MSD

MSD

15 open positions available

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MSD

Digital MMD Compliance Lead (Director)

MSDPrague, Prague, Czechia, Rahway, New Jersey, Durham, North Carolina, Upper Gwynedd Township, Pennsylvania, Elkton, Virginia, IrelandFull-time
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Compensation$90K - 130K a year

Lead and mentor compliance team ensuring IT alignment with global regulatory standards and oversee compliance strategy for capital investments. | Bachelor's degree with 10+ years IT compliance experience including 5 years managing teams and expertise in pharmaceutical regulations. | Job Description We aspire to be the premier research-intensive biopharmaceutical company. We're at the forefront of research to deliver innovative health solutions that advance the prevention and treatment of diseases in people and animals. We are seeking an experienced and proactive compliance leader to oversee our divisional compliance team to ensure regulatory alignment across our technology landscape. In this role, you will operate with a high degree of independence while championing a culture of transparency and knowledge sharing. You will serve as the vital link between IT and our broader business functions, ensuring that daily operations and major structural investments meet our rigorous global compliance standards. Responsibilities Build, lead, and mentor a high-performing team of compliance professionals. Successfully guide the team through ambiguity, competing priorities, and periods of complex organizational growth, fostering a resilient and adaptable team culture. Direct and oversee day-to-day IT operational compliance activities. Ensure that our ongoing IT processes, systems, and controls consistently meet internal standards and external regulatory requirements. Lead the IT compliance strategy and execution for large-scale capital investments. This includes ensuring all technology implementations for new facility builds and major upgrades to existing facilities are fully compliant from design through deployment. Act as the primary compliance liaison to key business units. Partner deeply with our Quality organization, the Global Engineering function, members of our Governance, Risk, and Compliance (GRC) team, and internal stakeholders to align objectives and streamline compliance efforts. Drive and manage global process improvement initiatives across the compliance landscape. This includes executing targeted, small-scale operational enhancements as well as steering large, complex, multi-regional enterprise programs. Drive compliance initiatives independently while maintaining open, transparent communication with leadership and stakeholders. Actively promote knowledge sharing across departments to elevate the organization’s overall understanding of IT compliance. Qualifications Required A bachelor’s degree (BA/BS) is required. A minimum of ten (10) years of progressive experience in IT compliance. At least five (5) years of direct experience leading and managing teams. Demonstrated ability to inspire and manage teams effectively during complex times of change, growth, and shifting prioritization. Demonstrated, deep knowledge of supporting and validating computerized systems within a global, highly regulated pharmaceutical environment. Expertise must extend well beyond US FDA regulations (e.g., 21 CFR Part 11). Must possess a comprehensive understanding of international health authority regulations and guidelines, including the EMA (Europe), MHRA (UK), and other relevant global standards (such as Annex 11, ICH guidelines, and GAMP 5 methodologies). A self-starter who excels at independent execution, values clear communication and transparent reporting, and possesses exceptional stakeholder management skills. Required Skills: Audit Management, Business Process Improvements, Data Modeling, FDA Regulations, Global Engineering, Governance Management, Information Systems Strategy, Information Technology Operations, Investment Compliance, IT Compliance Audit, IT Compliance Management, IT Performance Management, IT Security Compliance, Leadership, Pharmacy Regulation, Process Improvement Projects, Quality Assurance (QA), Regulatory Requirements, Stakeholder Relationship Management, Team Management, Technical Compliance Preferred Skills: Current Employees apply HERE Current Contingent Workers apply HERE US and Puerto Rico Residents Only: Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process. As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics. As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit: EEOC Know Your Rights EEOC GINA Supplement​ We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively. Learn more about your rights, including under California, Colorado and other US State Acts The salary range for this role is $173,200.00 - $272,600.00 This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employee’s position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs. The successful candidate will be eligible for annual bonus and long-term incentive, if applicable. We offer a comprehensive package of benefits. Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days. More information about benefits is available at https://jobs.merck.com/us/en/compensation-and-benefits. You can apply for this role through https://jobs.merck.com/us/en (or via the Workday Jobs Hub if you are a current employee). The application deadline for this position is stated on this posting. San Francisco Residents Only: We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance Los Angeles Residents Only: We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles’ Fair Chance Initiative for Hiring Ordinance Search Firm Representatives Please Read Carefully Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails. Employee Status: Regular Relocation: No relocation VISA Sponsorship: No Travel Requirements: 10% Flexible Work Arrangements: Hybrid Shift: 1st - Day Valid Driving License: No Hazardous Material(s): n/a Job Posting End Date: 08/11/2026 *A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.

IT Compliance Management
Governance Management
Leadership
Direct Apply
Posted 6 days ago
MSD

Associate Director, Global Data Management and Standards - Business Operations

MSDWarsaw, Masovian Voivodeship, Poland, Rahway, New Jersey, Upper Gwynedd Township, PennsylvaniaFull-time
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Compensation$90K - 130K a year

Drive enterprise-wide planning, governance, and organizational readiness for Global Data Management and Standards focusing on resource capacity planning and change management. | Bachelor's degree with 8+ years or advanced degree with 4+ years experience, strong analytical skills in Power BI/Tableau, and understanding of clinical data management and operational governance. | Job Description The Associate Director, Global Data Management and Standards - Business Operations, is responsible for collaborating with GDMS Leadership to drive enterprise-wide planning, governance, and organizational readiness initiatives that enable successful execution of strategic programs and projects. This role provides resource and capacity planning to ensure optimal allocation of talent, skills, and budget across the portfolio, while driving PMO standards, project governance, and performance reporting. The Associate Director partners with business leaders and key stakeholders to lead change management efforts, develop and execute communication strategies that promote transparency and stakeholder engagement, and champion learning and development initiatives that build organizational capabilities and support adoption of new processes, technologies, and ways of working. Through strong leadership, cross-functional collaboration, and a focus on continuous improvement, this position ensures the organization is equipped to deliver business objectives efficiently and sustainably. Responsibilities: Forecasting, Capacity, & Portfolio Management: Maintain headcount, workload, and demand models for the functional area; run allocation algorithms to help ensure the Book of Business is delivered with quality and timeliness. Support operating-model optimization within the functional area, translate outcomes into action plans and track through implementation. Manage real-time workload balancing, capacity, and compliance-driven case allocation across geographies within the functional area to ensure balanced operations, on-time delivery, and business continuity through holidays, resource availability, and demand peaks Build and maintain operational dashboards; collect, analyze, and validate portfolio data (efficiency, utilization, quality); ensure standardized reporting in partnership with cross-functional peers across GDMS (Global Data Management & Standards) and enterprise standards. Assist in developing forecasting tools, dashboards, and visualizations; contribute to continuous improvement of capacity modeling and workforce analytics. Support long-term quality management plans; participate in strategic and tactical special projects as needed. Operational Governance, Execution, & Metrics: Support PMO activities, including project planning, metrics tracking, status reporting, and management of cross-functional dependencies. Prepare inputs for Operational Reviews; ensure consistent metric definitions, sources, and timeframes per enterprise cadence and templates. Coordinate resource and financial forecasting, contracting, and invoicing; track variances and data integrity and publish reconciled views as required. Collaborate with stakeholders to maintain a unified set of metrics, training, and SOP/BP (Standard Operating Practice/ Best Practice) frameworks based on functional area needs. Monitor operational metrics post–system release to ensure realized efficiencies are captured in forecasting models and resource planning assumptions. Training, Communication, & Change Management: Support creation, maintenance, and delivery of role-specific curriculum; co-develop GDMS-wide training for the functional area; measure uptake. Coordinate function-specific communications and change management aligned to GDMS/GCTO (Global Clinical Trial Operations) frameworks. Embed Human-first Organization practices by designing adoption aids (FAQs, quick guides) and incorporating user feedback into process improvements. Qualifications, Skills & Experience: Technical Skills Ability to interpret operational, capacity, and financial data; comfortable with variance analysis and trends. Proficient with Power BI/Tableau and Excel (advanced modeling) for dashboards and what-if views. Working knowledge of capacity planning, resourcing, and portfolio management concepts. Familiarity with functional operational systems, performance dashboards, and workforce analytics data. Understanding of data integrity, metric standardization, and basic QC (Quality Control)/reconciliation practices. Basic grasp of forecasting, budgeting, and accruals; reads plan/forecast/actuals and ties them to operational drivers. Understanding of Agile collaboration and intake tracking tools for requests, changes, and release notes. Non-technical knowledge, skills, and abilities: Fluent in English; exceptional communication and influencing skills, able to engage and align stakeholders across functions, geographies, and levels. Strong stakeholder management and collaboration capabilities, fostering trust and effective partnerships. Skilled in organizing cross-team work; coordinates milestones and deliverables; escalates risks early. Demonstrated ability to lead through influence, motivating and guiding cross-functional and virtual teams without direct authority. Highly adaptable and resilient, able to prioritize and perform effectively under pressure in fast-changing environments. Works independently with accountability, exercising sound judgment and initiative while maintaining alignment with organizational priorities. Effective facilitator of decision-making, coordinating the work of others and driving timely resolution of complex issues. Crafts concise, decision-ready summaries for leadership, clearly framing risks, options, and recommendations. Strong organization and prioritization, managing multiple deliverables, running risk/change control, aligning stakeholders (including service providers), and providing status and governance updates. Sound judgment and accountability with emphasis on ambiguity, escalation management, and consensus-building on process/technology improvements. Enterprise Leadership Skills: Networking & Partnerships | Builds and sustains collaborative partnerships across GDMS, Finance, IT, and functional leaders to align forecasting assumptions, standardize metrics, and coordinate portfolio and resource priorities. Business Savviness | Applies strong operational and financial acumen to interpret portfolio performance, workforce capacity, and variance trends, guiding data-driven resource planning and efficiency decisions within the assigned scope. Influence | Influences cross-functional stakeholders by translating complex capacity, financial, and performance data into clear trade-offs, recommendations, and aligned action plans within governance forums. Business Operations Qualifications & Experience: Bachelor's Degree Minimum of 8 years experience working in relevant field for associated job description OR Advanced Degree (Masters or Doctorate): Minimum of 4 years experience working in relevant field for associated job description Required Skills: Adaptability, Business Acumen, Change Management, Clinical Data Management, Data Analysis, Good Clinical Practice (GCP), Strategic Thinking Preferred Skills: Current Employees apply HERE Current Contingent Workers apply HERE Search Firm Representatives Please Read Carefully Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails. Employee Status: Regular Relocation: No relocation VISA Sponsorship: No Travel Requirements: 10% Flexible Work Arrangements: Hybrid Shift: Not Indicated Valid Driving License: No Hazardous Material(s): n/a Job Posting End Date: 08/16/2026 *A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.

Capacity Planning
Portfolio Management
Change Management
Data Analysis
Power BI
Tableau
Clinical Data Management
Direct Apply
Posted 9 days ago
MSD

Associate Director, Supply Chain Management

MSDDublin, Leinster, Ireland, Lucerne, Lucerne, Switzerland, Rahway, New Jersey, Durham, North Carolina, Upper Gwynedd Township, PennsylvaniaFull-time
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Compensation$120K - 160K a year

Develop and execute end-to-end biologics product supply strategies, leading cross-functional teams to manage risks and lifecycle strategies ensuring supply continuity. | Bachelor's degree with 7+ years in large molecule operations, strong leadership in matrix environments, and knowledge of regulatory strategies and product lifecycles. | Job Description At our company, we aspire to be the premier research-intensive biopharmaceutical company. We're at the forefront of research to deliver innovative health solutions that advance the prevention and treatment of diseases in people and animals. We use the power of leading-edge science to save and improve lives around the world. Join us in our mission to make a difference. Value Chain Management (VCM) is the accountable organization for our company's Manufacturing Division product supply chain strategy in alignment with Global Human Health (GHH) brand/ franchise commercial goals. The Biologics VCM Product Manager (PM) works under direction of the VCM Product Leader supporting the development and execution of end-to-end (E2E) product supply strategies for one or more Biologics products. The VCM Product Manager will be responsible for supporting supply chain design, global filing and launch strategy, long-range demand vs capacity planning, integrated risk management, cost of goods projections, and post-approval product/ process/ supply chain change and lifecycle strategies for their product(s). As a result, VCM Product Managers have direct impact on cost, quality, customer service, and compliance which ultimately affects access, continuity of supply, and commercial outcomes. The VCM Product Manager will help lead the cross-functional Supply Chain Working Group (SCWG) for pipeline products or Value Chain Management Team (VCMT) for commercial products to develop and maintain a multi-year product strategy, prioritize key investments across the product supply chain, assure key project execution, and drive year on year attainment of brand operating metrics. VCM PM will help the SCWG/ VCMT to serve as a network level escalation team, to manage issues and risks escalated from sites and functions that require network level responses and communications. This is a highly integrative position, and it requires strong large molecule operations and technical knowledge as well as very strong leadership skills to help create the vision that guides and inspires the team and stakeholders. The role also requires strong team building skills and exceptional strength in communications. Responsibilities: Assist in leading cross functional Supply Chain Working Group (SCWG) for pipeline products or Value Chain Management Team (VCMT) for commercial products Support and/ or lead commercial siting selection, supply chain design, and value stream mapping Assist in gaining alignment and endorsement for supply chain strategic elements through senior stakeholder management and appropriate executive governance forums Develop and maintain product supply chain lifecycle strategies through Product Master Plans (PMP) as products are commercialized Support management of post-approval physical product enhancements, process and method technical changes, robustness/quality/ productivity projects Manage product supply chain Integrated Risk Management (IRM) and Business Continuity Planning (BCP), including identification & prioritization of mitigation strategies Assist in Global Filing and Launch (GFLS) strategy development to gain cross-divisional alignment on scope of market launches and associated timing Support development of Cost of Goods projections through the product lifecycle Support network/ platform strategies driven by pipeline evolution, and support associated cross-functional teams implementing manufacturing network capability/ expansion programs Help manage the interface with GHH on the global long-range demand forecast, and engage with VCM analytics COE on the development and maintenance of supply models and conducting scenario analysis in response to evolving global demand dynamics Engage in resolution of global product supply disruptions where long-term strategic supply chain alternatives need to be established Qualifications Required: Bachelor’s of Science degree in Engineering, Science, or Supply Chain Management Minimum of seven (7) years of relevant work experience Breadth of experience in large molecule (biologics/ vaccines) operations, technology, quality, and/ or supply chain Demonstrated ability to lead a cross-functional matrix teams through strategy/ project development and execution teams driving accountability through measured accomplishments Knowledge of the functions that support the business including the following: Product/ Process Development, Manufacturing Operations, Finance, Regulatory, Quality, Compliance, Supply Chain and Commercial Operations Understanding of manufacturing, testing and release processes for products supported. Understanding of regulatory strategy with respect to new product introduction (GFLS) and inline lifecycle management (change control) Understanding of product development lifecycle and integration of CMC and clinical strategy to bring a product to market. Ability to engage with our Research & Development division colleagues to ensure product is positioned to reliably launch with appropriate robustness and quality Ability to design and optimize product supply chains to deliver on necessary capacity, cost, and performance as measured by targeted SCM KPIs (lead time, inventory, COGs etc.) Strategic thinking and ability to assimilate highly complicated and multi-factored inputs into an integrated strategy that clearly links to business objectives and enterprise priorities Demonstrated ability to make timely decisions and influence direction in ambiguous situations Strong business acumen including understanding of financial product and network management as applied to key business processes such as business case/NPV analysis, product COGS interrogation and effective risk authorization stewardship. Understanding of product commercial strategy to inform supply strategy Assertiveness and ability to persuade and influence decisions along with driving accountability through measured accomplishments Proactive mindset and ability to look outside the assigned role with an eagerness to identify potential product and supply risks and engage in opportunities to improve business processes Proficiency in project and portfolio management tools and techniques Strong data analysis skills with competence in analyzing data sets and translating to drive business decision making Effective verbal and written communication skills with an ability to organize complex information in a concise and compelling manner Preferred: · Master’s of Science degree in Engineering, Science, or Supply Chain Management with eight (8) years of required work experience Required Skills: Business Continuity, Business Processes, Business Process Improvements, Clinical Supply Chain Management, Data Analysis, Driving Continuous Improvement, ERP Financial Systems, Inventory Control Management, Portfolio Management, Product Strategies, Strategic Planning, Supply Chain Design, Supply Chain Processes, Supply Change Management, Team-Building Preferred Skills: Current Employees apply HERE Current Contingent Workers apply HERE US and Puerto Rico Residents Only: Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process. As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics. As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit: EEOC Know Your Rights EEOC GINA Supplement​ We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively. Learn more about your rights, including under California, Colorado and other US State Acts The salary range for this role is $129,000.00 - $203,100.00 This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employee’s position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs. The successful candidate will be eligible for annual bonus and long-term incentive, if applicable. We offer a comprehensive package of benefits. Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days. More information about benefits is available at https://jobs.merck.com/us/en/compensation-and-benefits. You can apply for this role through https://jobs.merck.com/us/en (or via the Workday Jobs Hub if you are a current employee). The application deadline for this position is stated on this posting. San Francisco Residents Only: We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance Los Angeles Residents Only: We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles’ Fair Chance Initiative for Hiring Ordinance Search Firm Representatives Please Read Carefully Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails. Employee Status: Regular Relocation: No relocation VISA Sponsorship: No Travel Requirements: 10% Flexible Work Arrangements: Hybrid Shift: 1st - Day Valid Driving License: No Hazardous Material(s): n/a Job Posting End Date: 08/1/2026 *A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.

Supply Chain Management
Strategic Planning
Data Analysis
Direct Apply
Posted 9 days ago
MSD

Senior Specialist, Clinical Supply Project Manager - Inventory Manager – Hybrid

MSDRahway, New Jersey, Upper Gwynedd Township, PennsylvaniaFull-time
View Job
Compensation$55K - 90K a year

Manage strategic and operational plans for clinical supply movement, forecasting, and risk mitigation. | Bachelor's degree or 10+ years experience, 5+ years in project management and supply chain planning, SAP proficiency, GMP/GCP knowledge. | Job Description The Global Clinical Supply (GCS) organization is accountable for managing the 'end-to-end' integrated clinical supply chain across the full portfolio of clinical trials. GCS is accountable for the planning, sourcing, labelling, packaging and delivery of clinical supplies to clinical sites globally. The GCS Planning (Planning) organization is the key interface between clinical development teams and the operational/executional arms within the business. This role works within the Planning Execution and Inventory Management Section of the GCS Planning organization. Working independently, the Inventory Manager Clinical Supplies Project Manager (IM CSPM) creates strategic and operational plans associated with the downstream activities of clinical supplies for their assigned studies. The primary function of the IM CSPM is planning the availability of materials and subsequent movement through our depot network and further through to distribution and management of materials to the clinical site. The incumbent must have demonstrated understanding of E2E product development process & connectivity between functions supporting pipeline (i.e. clinical development, CMC, supply chain, & human health), and balancing needs of patients & ensuring stable supply of product. ​ Primary activities include, but are not limited to: Participates on the Clinical Trial Team (CTT) and collaborates closely with other functional area representatives to negotiate timelines and strategy for clinical supplies. Interacts with key partners in both GCS (Logistics and Trade, Distribution, Operations etc.) as well as other organizations such as Global Clinical Trial Operations (GCTO) headquarter and regional colleagues and Global Development Quality (GDQ) to address clinical supply related topics. Responsible and accountable for establishing the timelines for clinical supply needs per protocol and ensuring a robust signal for packaging and distribution for Clinical Finished Goods (CFGs) Analyzes and anticipates clinical study risks as they relate to clinical supply chain deliverables and prepares, analyzes, and/or develops mitigation strategies for review with clinical partners and senior leaders. Responsible and accountable for utilizing key tools/systems such as IRT & Microsoft PowerApps, SWMS, Veeva, MEDS, MyLearning, and other Microsoft Applications in the management of clinical supplies for assigned studies. Works directly in the SAP system to ensure a robust and consolidated forecast for CFGs is maintained. Report clinical supply chain incidents to support the gathering of metrics in GCS to describe business health. Participate in root causing to identify areas for operational improvement. Participates in initiation and timely processing of change controls through collaboration with GCS Planning and other cross functional stakeholders and in accordance with established GCS planning SOPs/BPs and QMS Topic 3.4 Change Control Procedures and Work Instructions. Participates in authoring and timely processing of deviation records as well as supports deviation investigations as required. Participates in critical non-pipeline and compliance activities in support of GCS Planning (e.g., process improvement initiatives, subject matter expert roles, SOP/BP development/maintenance, cross functional projects, etc.) Participates in supporting regulatory agency inspections for assigned trials as required. Demonstrates high capability to solve unstructured problems, make informed risk decisions considering both technical & business risks, & influence portfolio decisions with facts and data​ Demonstrates ability to balance strategy with ability for tactical execution and has strong ownership & accountability of assigned work​ Focus on Customers & Patients. Make rapid, disciplined decisions. Demonstrates Ethics & Integrity. Required Experience and Skills: Bachelor’s Degree in business, supply chain management, engineering or scientific discipline or High School Diploma with 10+ years equivalent industry experience in Pharmaceutical Clinical Supply (packaging, labeling, logistics and clinical supply inventory management) At least 5 years of experience in project management At least 5 years of experience in planning, scheduling, coordination and processing of supply chain activities, or the equivalent Excellent Communication & Interpersonal Skills: ability to effectively communicate with stakeholders at various levels, including cross-functional teams, senior management, external vendors, and clinical sites. Strong negotiation, influencing, and relationship-building skills to ensure alignment and collaboration in the supply planning process.​ Project Management Skills: strong knowledge of the principles of project management and clinical customer relationship management. Technical Proficiency: familiarity with supply chain systems and software (e.g. SAP or Oracle) and demand planning principles as well as Microsoft Excel, PowerPoint, and Word Strong Analytical & Problem Solving Skills: ability to analyze complex data, identify trends, and make data-driven decisions to optimize supply chain processes. Flexibility & Adaptability: Demonstrates ability to thrive in a fast-paced and dynamic environment, with the capability to adapt quickly to changing business needs and priorities.​ Detail Oriented & Organized: strong attention to detail in managing complex supply chain activities; ability to multitask, prioritize tasks, and meet tight deadlines.​ Continuous Improvement Mindset: Proactive approach to identify process inefficiencies, develop solutions, and drive continuous improvement initiatives within the clinical supply planning function. Proficiency in using supply chain management systems and software, including experience with ERP systems (e.g., SAP), demand planning tools, and inventory management systems. Proven record in project / portfolio management. Knowledge of Good Manufacturing Practices (GMP) and Good Clinical Practices (GCP) is highly desirable. Preferred Experience and Skills: Results-orientation with the proven ability to execute on collaborative projects and develop subject matter expertise Knowledge of order management, supply chain operations and document control. #eligibleforERP GCScareer26 #MSJR Required Skills: Adaptability, Adaptability, Business Risks, Change Management, Clinical Development, Clinical Supplies Management, Clinical Supply Chain Management, Clinical Trial Management, Complex Data Analysis, Cross-Functional Leadership, Data Analysis, Demand Planning, Detail-Oriented, Deviation Investigations, Good Manufacturing Practices (GMP), Interpersonal Relationships, Inventory Management, Key Performance Indicators (KPI), Materials Requirements Planning (MRP), Portfolio Management, Process Improvement Projects, Project Management, Risk Management, Supply Chain Optimization, Supply Chain Systems {+ 2 more} Preferred Skills: Current Employees apply HERE Current Contingent Workers apply HERE US and Puerto Rico Residents Only: Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process. As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics. As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit: EEOC Know Your Rights EEOC GINA Supplement​ We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively. Learn more about your rights, including under California, Colorado and other US State Acts The salary range for this role is $117,000.00 - $184,200.00 This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employee’s position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs. The successful candidate will be eligible for annual bonus and long-term incentive, if applicable. We offer a comprehensive package of benefits. Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days. More information about benefits is available at https://jobs.merck.com/us/en/compensation-and-benefits. You can apply for this role through https://jobs.merck.com/us/en (or via the Workday Jobs Hub if you are a current employee). The application deadline for this position is stated on this posting. San Francisco Residents Only: We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance Los Angeles Residents Only: We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles’ Fair Chance Initiative for Hiring Ordinance Search Firm Representatives Please Read Carefully Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails. Employee Status: Regular Relocation: No relocation VISA Sponsorship: No Travel Requirements: 10% Flexible Work Arrangements: Hybrid Shift: 1st - Day Valid Driving License: Yes Hazardous Material(s): No Job Posting End Date: 07/24/2026 *A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.

Clinical Supply Chain Management
Project Management
Inventory Management
Demand Planning
SAP
Risk Management
Direct Apply
Posted 12 days ago
MSD

Director, Cybersecurity Engineering

MSDRahway, New JerseyFull-time
View Job
Compensation$90K - 150K a year

Lead proof of concept exercises and oversee engineering of complex security systems across environments. | Bachelor's degree with 5+ years in people and engineering leadership for enterprise initiatives, strong innovation and communication skills. | Job Description Our company is looking for a leader to join our Cyber Rapid Innovation organization to spearhead new technology initiatives. This leader serves as an enterprise-wide point of contact and SME for emerging technologies and how they impact our overall security footprint. Additionally, this individual will serve as a liaison between our company and the broader cyber industry and community. If you are passionate about cybersecurity and innovation, and thrive in a dynamic environment, we invite you to join our team and make a significant impact. This is a hybrid role (3 days in the office) based in Rahway, NJ Responsibilities Lead end-to-end proof of concept exercises for our CISO organization Interface with vendors, peers, and the broader industry to stay on top of new and emerging technologies in the security ecosystem Oversee the engineering and implementation of complex security systems bo.th on-premises and in the cloud Build a strong internal network to ensure cohesion across multiple business verticals Ensure engineering excellence is front and center as new solutions are brought in and enabled Minimum Qualifications Bachelor’s degree in related field Minimum five years of managerial experience in people leadership, with the ability to inspire and guide teams At least 5 years' experience in Engineering leadership experience, with a specific focus on large enterprise-scale initiatives Strong written communication skills, with the ability to articulate complex concepts clearly Demonstrated innovation in the field of technology and/or cybersecurity Adept at networking and building partnerships within the industry Commitment to execution excellence, ensuring high standards in all projects Strong analytical thinking skills, with the ability to solve complex problems Required Skills: Application Security, Application Security, Certificate Services, Change Catalyst, Communication, Cross-Cultural Awareness, Cybersecurity, Cybersecurity Analytics, Cybersecurity Operations, Delivery of Security Applications, Design Applications, Emerging Technologies, Establishing Contacts, Information Security, Leadership, Liaison Communications, Network Segmentation, Operational Technology (OT) Security, Project Management, Project Planning, Security Compliance, SLA Management, Strategic Initiative, Systematic Problem Solving, System Designs {+ 3 more} Preferred Skills: Current Employees apply HERE Current Contingent Workers apply HERE US and Puerto Rico Residents Only: Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process. As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics. As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit: EEOC Know Your Rights EEOC GINA Supplement​ We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively. Learn more about your rights, including under California, Colorado and other US State Acts The salary range for this role is $156,900.00 - $247,000.00 This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employee’s position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs. The successful candidate will be eligible for annual bonus and long-term incentive, if applicable. We offer a comprehensive package of benefits. Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days. More information about benefits is available at https://jobs.merck.com/us/en/compensation-and-benefits. You can apply for this role through https://jobs.merck.com/us/en (or via the Workday Jobs Hub if you are a current employee). The application deadline for this position is stated on this posting. San Francisco Residents Only: We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance Los Angeles Residents Only: We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles’ Fair Chance Initiative for Hiring Ordinance Search Firm Representatives Please Read Carefully Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails. Employee Status: Regular Relocation: Domestic VISA Sponsorship: No Travel Requirements: 10% Flexible Work Arrangements: Hybrid Shift: 1st - Day Valid Driving License: No Hazardous Material(s): N/a Job Posting End Date: 07/24/2026 *A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.

Cybersecurity Operations
OT Security
Leadership
Direct Apply
Posted 16 days ago
MSD

Associate Director, US Strategy & Planning

MSDNorth Wales, PennsylvaniaFull-time
View Job
Compensation$75K - 120K a year

Lead development of long-term US commercial strategies and data-driven resource prioritization frameworks. | Bachelor's degree with 5+ years in strategy, marketing, sales, or commercial operations and strong executive presence in healthcare. | Job Description The Associate Director, US Commercial Strategy is a critical contributor on the US Market Strategy team which is responsible for Commercial Strategy, Launch Strategy and Operations and Customer Experience in the US Market. The Associate Director, US commercial strategy, will work in close partnership with leadership across Oncology, Specialty, Pharma & ID, Commercial Excellence & Innovation and Digital Human Health. As a member of the US Commercial Strategy team, this position partners to develop long-term commercial strategy and identify opportunity spaces by working in close partnership with key stakeholders, to include the US Country Council Leadership Team. This position reports to the Director, US Commercial Strategy Lead. Primary Responsibilities: Support the development of a long-term Commercial Strategy to guide the US market’s ongoing commercial transformation. Strategy Development: Lead end-to-end strategy support—define opportunity spaces, structure approaches, conduct analyses, translate insights into Commercial Strategy, align stakeholders through workshops, and deliver executive-ready presentations. Translate strategic opportunity spaces into now/near/next strategic blueprints with realization owners. Partner on high-priority strategic initiatives that will drive transformational impact and position the US market, for future success. Resource Prioritization & Optimization: Develop frameworks and models to support data-driven resource allocation decisions across products and functions. Identify critical assumptions and prioritization model logic. Ability to generate strategic insights from data and apply those insights to strategic opportunity spaces. Work with corporate & global strategy, to ensure tight integration with the US Market. Build effective and sustainable partnerships with internal stakeholders, as well as leading external organizations, to ensure that our US commercial strategy is forward looking, well-rounded and represented in the appropriate healthcare context. Position Qualifications: Education Minimum Requirement: Required: BA/BS degree. Preferred: MBA or MPH degree. Required Experience and Skills: Minimum of 5 years of work experience to include Strategy Development, Marketing, Sales, Access / Policy, Commercial Operations, and/or Organizational transformation. Strong executive presence to include advanced written and verbal skills. Ability to analyze external and industry trends, form educated opinions and deliver tangible recommendations to key stakeholders. Understanding of US / Global Healthcare ecosystem. Energized by working in a collaborative, fast-paced environment in strong partnership with peers and key stakeholders, both within and outside the US market. Strong vision for the future, with the ability to inspire change, translate data into business implications, gain support, and partner to drive organizational transformation and operating model evolution. Exceptional working knowledge of MS Office applications, including PPT, Excel and Word. Inspire impact through strong collaborative relationships. Ability to lead without direct influence. Demonstrates high degree of ethics and integrity. Required Skills: Adaptability, Adaptability, Agile Project Management, Business Strategies, Commercial Strategies, Corporate Strategy Development, Customer Satisfaction, Data-Driven Decision Making, Developing Proposals, Employee Performance Evaluations, Environmental Scanning, Executive Presence, Feasibility Studies, Global Strategy, IT Demand Management, Market Research, Pharmaceutical Market, Portfolio Management, Prioritization, Project Management, Resource Allocation, Risk Management, Stakeholder Engagement, Strategic Initiative, Strategic Insights {+ 2 more} Preferred Skills: Current Employees apply HERE Current Contingent Workers apply HERE US and Puerto Rico Residents Only: Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process. As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics. As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit: EEOC Know Your Rights EEOC GINA Supplement We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively. Learn more about your rights, including under California, Colorado and other US State Acts The salary range for this role is $142,400.00 - $224,100.00 This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employee’s position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs. The successful candidate will be eligible for annual bonus and long-term incentive, if applicable. We offer a comprehensive package of benefits. Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days. More information about benefits is available at https://jobs.merck.com/us/en/compensation-and-benefits. You can apply for this role through https://jobs.merck.com/us/en (or via the Workday Jobs Hub if you are a current employee). The application deadline for this position is stated on this posting. San Francisco Residents Only: We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance Los Angeles Residents Only: We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles’ Fair Chance Initiative for Hiring Ordinance Search Firm Representatives Please Read Carefully Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails. Employee Status: Regular Relocation: Domestic VISA Sponsorship: No Travel Requirements: 10% Flexible Work Arrangements: Hybrid Shift: 1st - Day Valid Driving License: No Hazardous Material(s): n/a Job Posting End Date: 08/15/2026 *A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date. Our company is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where we have codified our legacy for over a century. Our success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare.

Strategy Development
Commercial Strategy
Resource Allocation
Direct Apply
Posted 18 days ago
MSD

Dir , Technical Product Management, Content Supply Chain Orchestration

MSDRahway, New Jersey, North Wales, PennsylvaniaFull-time
View Job
Compensation$85K - 130K a year

Lead strategic direction and operating model for enterprise content supply chain orchestration focusing on standardization and automation globally. | 8+ years leading complex technology-enabled business transformations in regulated environments with a bachelor's degree; preference for pharmaceutical or healthcare experience. | Job Description The Director, Content Supply Chain Orchestration is accountable for defining and leading the strategic direction, operating model, and execution of an enterprise content supply chain orchestration capability that enables faster, higher-quality, and more cost-effective content creation at scale. This role translates business priorities into an integrated content supply chain strategy that supports global product launches, omnichannel engagement, and reuse of approved content across markets and brands. This leader owns the orchestration layer across people, process, data, and technology, with responsibility for standardization, governance, automation, and value realization across the end-to-end content lifecycle. The role requires strong strategic leadership in a highly matrixed, regulated environment, including the ability to influence senior leaders, shape enterprise decisions, lead global transformation, and build high-performing teams that deliver measurable business impact. Required Experience & Qualifications: 8+years experience leading complex, technology-enabled business transformation in global, matrixed organizations, with demonstrated accountability for enterprise outcomes and cross-functional delivery. Proven success designing, scaling, and governing operating models, workflows, or platforms that improve speed, quality, compliance, and efficiency across an end-to-end process. Strong experience partnering with senior stakeholders across business, technology, operations, and compliance functions to shape strategy, drive alignment, and manage complex trade-offs. Demonstrated track record leading organizational change, global rollouts, and adoption of new capabilities in regulated environments, including management of risk, dependencies, and value realization. Experience building, leading, and developing high-performing teams, including coaching leaders and fostering an inclusive, accountable, and growth-oriented culture. Strong understanding of pharmaceutical, healthcare, or other highly regulated business environments, including the importance of governance, compliance, and quality. Preferred experience with content supply chain, digital asset management, workflow orchestration, metadata strategy, and Adobe-based or related enterprise platforms. This role will report into Executive Director, Content Enablement & Execution and will lead up to 10 members of the product team. Necessary Competencies: · Strategic enterprise mindset with the ability to connect operational decisions to business outcomes and long-term capability building. · Strong leadership presence and executive communication skills, with the ability to influence and align senior stakeholders in a complex matrix. · High learning agility and sound judgment, with the ability to navigate ambiguity, assess trade-offs, and make decisions at pace. · Strong change leadership capabilities, including the ability to inspire adoption, sustain momentum, and embed new ways of working. · Inclusive people leader who develops talent, builds trust, and creates an environment of accountability, collaboration, and continuous improvement Education Minimum Requirement: Bachelor’s degree in business, technology, engineering, life sciences, or a related field required. Advanced degree preferred. Key Accountabilities 1. Strategy, Operating Model, and Governance · Define and evolve the enterprise strategy, operating model, and governance for content supply chain orchestration, aligned to business priorities, launch needs, and long-term capability goals.· Establish decision frameworks, standards, and guardrails that enable consistency, scale, compliance, and efficient execution across the end-to-end content lifecycle.· Translate strategic objectives into prioritized roadmaps, clear success measures, and sequenced delivery plans across people, process, data, and technology. 2. End-to-End Process Design and Orchestration· Own the design and continuous improvement of scalable, standardized workflows spanning intake, planning, creation, review, approval, distribution, reuse, and retirement of content.· Balance enterprise standardization with market and brand needs, ensuring the operating model supports both global consistency and local execution requirements.· Identify opportunities to reduce cycle time, improve quality, eliminate duplication, and increase reuse through simplification and orchestration. 3. Data, Metadata, and Automation· Lead the enterprise approach to taxonomy, metadata, and tagging standards to improve findability, reuse, reporting, and downstream optimization.· Drive automation opportunities across the content supply chain, leveraging workflow and platform capabilities to improve efficiency, control, and user experience.· Partner with data, analytics, and platform teams to ensure orchestration capabilities generate actionable insights and measurable business value. 4. Platform Enablement and Transformation Delivery· Provide business leadership for orchestration-related platform capabilities, including prioritization of enhancements, integrations, and rollout sequencing.· Lead large-scale transformation and migration efforts from legacy tools and fragmented ways of working into a standardized future-state ecosystem.· Ensure delivery is achieved with clear governance, strong dependency management, disciplined risk mitigation, and minimal business disruption. 5. Stakeholder Leadership and Enterprise Influence· Serve as a trusted strategic partner to senior leaders across business, operations, technology, legal, regulatory, medical, and external partners.· Influence enterprise decisions by articulating trade-offs, risks, and recommendations clearly, and by building alignment across stakeholder groups without direct authority.· Communicate progress, issues, and outcomes to leadership with clarity and transparency, reinforcing accountability and confidence in delivery. 6. People Leadership and Capability Building· Lead, coach, and develop a high-performing global team, building depth in strategic thinking, execution excellence, and change leadership.· Create an inclusive and accountable culture that encourages collaboration, innovation, continuous improvement, and strong talent development.· Assess capability gaps and build the organizational structures, roles, and development plans needed to sustain long-term success. Success Criteria for the role: · A clear enterprise content supply chain strategy and operating model is defined, adopted, and governed across priority areas. · Measurable improvements are achieved in speed, reuse, quality, compliance, and cost efficiency across the content lifecycle. · Platform, workflow, and migration initiatives are delivered with strong adoption, controlled risk, and sustained business value. · Senior stakeholders view the function as a trusted partner that brings clarity, structure, and forward momentum to complex transformation efforts. · The organization demonstrates strong engagement, capability growth, and leadership bench strength within the team. Required Skills: Asset Management, Benefits Management, Business Transformation, Global Rollouts, Global Team Collaboration, Global Transformation, Life Science, Management System Development, Operating Models, Operational Decisions, Process Orchestration, Product Management, Requirements Management, Risk Management, Risk Mitigation Strategies, Stakeholder Relationship Management, Strategic Leadership, Strategic Planning, Strategic Thinking, System Designs Preferred Skills: Current Employees apply HERE Current Contingent Workers apply HERE US and Puerto Rico Residents Only: Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process. As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics. As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit: EEOC Know Your Rights EEOC GINA Supplement We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively. Learn more about your rights, including under California, Colorado and other US State Acts The salary range for this role is $173,200.00 - $272,600.00 This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employee’s position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs. The successful candidate will be eligible for annual bonus and long-term incentive, if applicable. We offer a comprehensive package of benefits. Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days. More information about benefits is available at https://jobs.merck.com/us/en/compensation-and-benefits. You can apply for this role through https://jobs.merck.com/us/en (or via the Workday Jobs Hub if you are a current employee). The application deadline for this position is stated on this posting. San Francisco Residents Only: We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance Los Angeles Residents Only: We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles’ Fair Chance Initiative for Hiring Ordinance Search Firm Representatives Please Read Carefully Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails. Employee Status: Regular Relocation: No relocation VISA Sponsorship: No Travel Requirements: 25% Flexible Work Arrangements: Hybrid Shift: Not Indicated Valid Driving License: No Hazardous Material(s): n/a Job Posting End Date: 07/24/2026 *A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date. Our company is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where we have codified our legacy for over a century. Our success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare.

Strategic Leadership
Supply Chain Management
S&OP Leadership
Direct Apply
Posted 24 days ago
MS

Lead Architect, Data Context Layer

MSDRahway, New Jersey, North Wales, PennsylvaniaFull-time
View Job
Compensation$120K - 160K a year

Define and guide the conceptual and technical architecture for an enterprise Data Context Layer platform to enable self-service publishing and consumption of standardized data context. | Bachelor's degree and 8+ years in enterprise, solution, or data architecture with expertise in semantic technologies and AI infrastructure. | Job Description Role Overview This role is part of a broader enterprise initiative to establish a Data Context Layer (DCL) — a foundational capability designed to provide consistent, reusable, and scalable context across enterprise data products. The DCL is intended to address challenges related to data fragmentation, lack of shared semantics, and inconsistent interpretation of data across systems and products. It establishes a unified layer for representing context, relationships, and meaning, enabling downstream products to operate with greater consistency, interoperability, and intelligence. In addition, the DCL plays a critical role in enabling agentic AI capabilities across the enterprise by providing the structured context and semantic grounding required for intelligent agents to operate reliably. This includes ensuring that agent-driven workflows and decisions are based on consistent, governed, and interpretable data context, reducing risks associated with fragmentation, ambiguity, and lack of control. Within this initiative, we are seeking a Lead Architect to define and guide the conceptual and technical architecture for an enterprise platform that enables teams to publish, discover, and consume standardized data context through self-service. This role will shape the target architecture, integration patterns, and technical standards that support scalable, secure, and production-ready context services across the enterprise. The ideal candidate has deep experience in enterprise architecture, data platforms, semantic technologies, and AI-enabled systems. Familiarity with ontologies, OWL, metadata-driven architectures, agentic AI, prompt engineering, and context engineering is required, as the platform must support both human and AI-driven consumers of context. Key Responsibilities Define the target architecture for the enterprise data context self-service platform. Establish architectural standards and patterns for: context publishing discovery access control versioning validation lineage and provenance observability and monitoring Partner with product, engineering, service design, security, and governance teams to ensure the platform is technically sound and aligned to enterprise needs. Evaluate and recommend technologies and integration patterns including: ontology and semantic modeling approaches OWL/RDF-based systems knowledge graphs semantic layers MCP, A2A, and Timbr-like technologies where applicable Design architecture that supports both self-service user workflows and AI/agentic consumption patterns. Ensure context can move from development to production in a governed, scalable, and supportable way. Define non-functional requirements including performance, resilience, security, compliance, and operational maintainability. Review solution designs and implementation plans to ensure adherence to architectural standards. Create reference architectures, patterns, and decision records to guide implementation teams. Collaborate with platform teams to support long-term scalability, reuse, and interoperability across domains. Help shape how the platform supports agentic AI workflows, including structured prompt context, tool access, and reliable data grounding. Minimum Required Qualifications Bachelors degree 8+ years of experience in enterprise architecture, solution architecture, data architecture, or platform architecture. Strong technical background in data platforms, metadata systems, semantic technologies, or AI infrastructure. Familiarity with ontologies, OWL, RDF, knowledge graphs, and semantic layer concepts. Experience designing platforms that support self-service, enterprise-scale reuse, and governed access. Expertise in agentic AI, prompt engineering, and context engineering concepts. Experience defining and enforcing technical standards across multiple teams. Strong ability to communicate architecture decisions to both technical and non-technical stakeholders. Preferred Qualifications Experience with MCP, A2A, Timbr, or similar context-serving or semantic interoperability technologies. Background in enterprise data governance, metadata management, or data catalog architectures. Experience supporting AI-enabled platforms or agentic workflows. Knowledge of production concerns such as observability, testing, CI/CD, identity and access management, and lifecycle management. Experience creating reference architectures and reusable patterns for platform teams. Familiarity with regulated or security-sensitive enterprise environments. What Success Looks Like Success in this role means: the platform has a clear, scalable Conceptual/Technical architecture context is served consistently and securely across the enterprise teams can build and integrate using reusable patterns development-to-production flows are reliable and governed the platform supports both enterprise applications and AI/agentic use cases architectural decisions reduce duplication and increase long-term maintainability Required Skills: Context Mapping, Data Modeling, Design Applications, Enterprise Architecture (EA), Enterprise Architecture Management, Enterprise Data, Enterprise Data Management, Enterprise Security Operations, Metadata, Metadata Management, Ontology, Prompt Engineering, Reference Architectures, Release Management, Requirements Management, Semantic Web, Solution Architecture, System Designs, System Integration Preferred Skills: Current Employees apply HERE Current Contingent Workers apply HERE US and Puerto Rico Residents Only: Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process. As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics. As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit: EEOC Know Your Rights EEOC GINA Supplement We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively. Learn more about your rights, including under California, Colorado and other US State Acts The salary range for this role is $142,400.00 - $224,100.00 This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employee’s position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs. The successful candidate will be eligible for annual bonus and long-term incentive, if applicable. We offer a comprehensive package of benefits. Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days. More information about benefits is available at https://jobs.merck.com/us/en/compensation-and-benefits. You can apply for this role through https://jobs.merck.com/us/en (or via the Workday Jobs Hub if you are a current employee). The application deadline for this position is stated on this posting. San Francisco Residents Only: We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance Los Angeles Residents Only: We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles’ Fair Chance Initiative for Hiring Ordinance Search Firm Representatives Please Read Carefully Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails. Employee Status: Regular Relocation: No relocation VISA Sponsorship: No Travel Requirements: 10% Flexible Work Arrangements: Hybrid Shift: 1st - Day Valid Driving License: No Hazardous Material(s): N/A Job Posting End Date: 07/13/2026 *A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date. Our company is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where we have codified our legacy for over a century. Our success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare.

Business Intelligence
Data Analytics
Python
R
SQL
IBM Cognos
Tableau
Power BI
AI Prompt Engineering
Direct Apply
Posted 27 days ago
MS

Director, Portfolio Lead Intercontinental – Pharma / Specialty (m/f/d)

MSDLucerne, Lucerne, Switzerland, Rahway, New Jersey, Upper Gwynedd Township, PennsylvaniaFull-time
View Job
Compensation$90K - 130K a year

Lead franchise performance and strategic alignment for pharma portfolio across regions ensuring launch readiness. | Requires 10+ years in pharma commercial operations or consulting with a bachelor's and preferably a postgraduate degree. | Job Description Reports to: AVP Intercontinental Business Operations Position Summary The Intercontinental Portfolio Lead is a critical leadership role within the Intercontinental (IC) Regional Team, responsible for driving franchise performance, execution excellence, and strategic alignment across the Pharma/Specialty portfolio. The Portfolio Lead will ensure effective translation of strategy into execution, accelerate launch readiness, and deliver sustained performance across markets, while serving as the primary interface between Global Franchises and the Intercontinental Region. In addition, the Portfolio Lead is accountable for leading 1–2 high-impact cross-regional strategic initiatives, focused on advancing capabilities, improving execution models, and unlocking growth across Intercontinental markets. The role requires deep enterprise and commercial strategic expertise, a hands-on execution-focused leadership approach, and a strong understanding of the Intercontinental business. Success requires strong analytical skills to generate insights and actionable plans, exceptional influencing skills with tact and diplomacy, and a proven track record of business leadership, collaboration, and delivering results in a dynamic, fast-paced environment. Position Responsibilities Franchise Leadership & Regional Stewardship Act as the IC lead and spokesperson for the Pharma/Specialty franchise Lead and coordinate the IC franchise community and squads across regions Drive alignment of strategy, priorities, and execution across markets and sub-regions (CMOs/RCLs in AP, EEMEA, and LATAM) Represent IC perspectives in global discussions and governance Act as the primary interface between Global Franchises and Intercontinental, building strong partnerships across global, regional, and local stakeholders Strategy Execution & Performance Management Consolidate global strategies into clear, actionable regional priorities Monitor, consolidate, and report business performance across the portfolio Identify risks and opportunities and drive proactive course correction Ensure disciplined execution against financial and strategic objectives Launch Excellence & Portfolio Acceleration Coordinate regional efforts for launch readiness and launch excellence Drive lifecycle management priorities and portfolio optimization Support execution across both launch and in-line assets Strategic Initiatives & Capability Building Lead 1–2 cross-regional strategic projects such as localizations, commercial business development, above-market partnerships, and capability deployment in coordination with cross-functional teams (Access, Policy, BD, DHH) Required Experience and Skills Minimum of 10 years of progressive experience across marketing, sales, access, commercial operations or related experiences in pharmaceutical or management consulting company Bachelor’s degree required; Advanced degree (MBA, MSc, or equivalent) preferred Proven track record in commercial strategy and execution, launch excellence and/or portfolio management, leading complex, cross-functional initiatives Exposure to multiple markets and diverse healthcare systems Preferred Experience and Skills Depth of Therapeutic Area expertise in Pharma/Specialty, coupled with the Intercontinental region experience (Market experience is a strong plus (P&L and people management)) Depth of Marketing, Market Access understanding and P&L management, as well as a fundamental understanding of the Intercontinental business Leadership and Impact: Proven track record of high-performance launches and driving business results Collaboration & Influence without authority: Strong collaboration skills, both within commercial teams and cross divisional teams including R&D and manufacturing, medical affairs, Outcomes Research and Access Communication: Ability to clearly articulate messages/information across the enterprise and to all levels, including highest levels of senior leadership Strategic Thinking: Proven ability to analyze complex data and create clear patient and customer centric strategies Challenging Status Quo: Ability to push past internal obstacles to drive initiatives forward Travel Position requires up to 30-50 % travel Location Preference is for this role to be based in Lucerne, Switzerland (Intercontinental HQ). Relocation support can be provided to the successful candidate, if required. The role may also be based in the United States, in Rahway or Upper Gwynedd. Only U.S.-based local candidates will be considered for U.S.-based positions, and no visa or relocation support to the United States will be provided. ++++++++++++++++++++++++++++++++++++ US and Puerto Rico Residents Only: Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process. As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics. As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit: EEOC Know Your Rights EEOC GINA Supplement We are proud to be a company that embraces the value of bringing together, talented, and committed people with varied experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with varied ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively. Learn more about your rights, including under California, Colorado and other US State Acts U.S. Hybrid Work Model Effective September 5, 2023, employees in office-based positions in the U.S. will be working a Hybrid work consisting of three total days on-site per week, Monday - Thursday, although the specific days may vary by site or organization, with Friday designated as a remote-working day, unless business critical tasks require an on-site presence. This Hybrid work model does not apply to, and daily in-person attendance is required for, field-based positions; facility-based, manufacturing-based, or research-based positions where the work to be performed is located at a Company site; positions covered by a collective-bargaining agreement (unless the agreement provides for hybrid work); or any other position for which the Company has determined the job requirements cannot be reasonably met working remotely. Please note, this Hybrid work model guidance also does not apply to roles that have been designated as “remote”. The salary range for this role is $190,800.00 - $300,300.00 This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employee’s position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs. The successful candidate will be eligible for annual bonus and long-term incentive, if applicable. We offer a comprehensive package of benefits. Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days. More information about benefits is available on our US Compensation and Benefits homepage US Compensation and Benefits homepage. You can apply for this role through career page, (or via the Workday Jobs Hub if you are a current employee). The application deadline for this position is stated on this posting. San Francisco Residents Only: We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance Los Angeles Residents Only: We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles’ Fair Chance Initiative for Hiring Ordinance Search Firm Representatives Please Read Carefully We do not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails. Required Skills: Commercial Strategies, Cross-Functional Leadership, Data-Driven Decision Making, Executive Communications, Influence, Launch Excellence, Portfolio Management, Profit and Loss (P&L), Strategic Thinking Preferred Skills: Speciality Pharmaceuticals Current Employees apply HERE Current Contingent Workers apply HERE Search Firm Representatives Please Read Carefully Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails. Employee Status: Regular Relocation: International VISA Sponsorship: Yes Travel Requirements: 50% Flexible Work Arrangements: Hybrid Shift: Not Indicated Valid Driving License: No Hazardous Material(s): no Job Posting End Date: 07/20/2026 *A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date. Our company is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where we have codified our legacy for over a century. Our success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare.

Business Intelligence
Data Analysis
Audit Data Analytics
Direct Apply
Posted 28 days ago
MS

Director, Portfolio Lead Intercontinental – Vaccines & Infectious Disease (m/f/d)

MSDLucerne, Lucerne, Switzerland, Rahway, New Jersey, Upper Gwynedd Township, PennsylvaniaFull-time
View Job
Compensation$120K - 180K a year

Lead vaccine and infectious disease portfolio across region to drive franchise performance and strategic alignment. | Requires 10+ years in pharmaceutical commercial operations or management consulting with advanced degree preferred. | Job Description Reports to: AVP Intercontinental Business Operations Position Summary The Intercontinental Portfolio Lead is a critical leadership role within the Intercontinental (IC) Regional Team, responsible for driving franchise performance, execution excellence, and strategic alignment across the Vaccines & Infectious Disease portfolio. The Portfolio Lead will ensure effective translation of strategy into execution, accelerate launch readiness, and deliver sustained performance across markets, while serving as the primary interface between Global Franchises and the Intercontinental Region. In addition, the Portfolio Lead is accountable for leading 1–2 high-impact cross-regional strategic initiatives, focused on advancing capabilities, improving execution models, and unlocking growth across Intercontinental markets. The role requires deep enterprise and commercial strategic expertise, a hands-on execution-focused leadership approach, and a strong understanding of the Intercontinental business. Success requires strong analytical skills to generate insights and actionable plans, exceptional influencing skills with tact and diplomacy, and a proven track record of business leadership, collaboration, and delivering results in a dynamic, fast-paced environment. Position Responsibilities Franchise Leadership & Regional Stewardship Act as the IC lead and spokesperson for the Vaccines & Infectious Disease franchise Lead and coordinate the IC franchise community and squads across regions Drive alignment of strategy, priorities, and execution across markets and sub-regions (CMOs/RCLs in AP, EEMEA, and LATAM) Represent IC perspectives in global discussions and governance Act as the primary interface between Global Franchises and Intercontinental, building strong partnerships across global, regional, and local stakeholders Strategy Execution & Performance Management Consolidate global strategies into clear, actionable regional priorities Monitor, consolidate, and report business performance across the portfolio Identify risks and opportunities and drive proactive course correction Ensure disciplined execution against financial and strategic objectives Launch Excellence & Portfolio Acceleration Coordinate regional efforts for launch readiness and launch excellence Drive lifecycle management priorities and portfolio optimization Support execution across both launch and in-line assets Strategic Initiatives & Capability Building Lead 1–2 cross-regional strategic projects such as localizations, commercial business development, above-market partnerships, and capability deployment in coordination with cross-functional teams (Access, Policy, BD, DHH) Required Experience and Skills Minimum of 10 years of progressive experience across marketing, sales, access, commercial operations or related experiences in pharmaceutical or management consulting company Bachelor’s degree required; Advanced degree (MBA, MSc, or equivalent) preferred Proven track record in commercial strategy and execution, launch excellence and/or portfolio management, leading complex, cross-functional initiatives Exposure to multiple markets and diverse healthcare systems Preferred Experience and Skills Depth of Therapeutic Area expertise in Vaccines & Infectious Diseases, coupled with the Intercontinental region experience (Market experience is a strong plus (P&L and people management)) Depth of Marketing, Market Access understanding and P&L management, as well as a fundamental understanding of the Intercontinental business Leadership and Impact: Proven track record of high-performance launches and driving business results Collaboration & Influence without authority: Strong collaboration skills, both within commercial teams and cross divisional teams including R&D and manufacturing, medical affairs, Outcomes Research and Access Communication: Ability to clearly articulate messages/information across the enterprise and to all levels, including highest levels of senior leadership Strategic Thinking: Proven ability to analyze complex data and create clear patient and customer centric strategies Challenging Status Quo: Ability to push past internal obstacles to drive initiatives forward Travel Position requires up to 30-50 % travel Location Preference is for this role to be based in Lucerne, Switzerland (Intercontinental HQ). Relocation support can be provided to the successful candidate, if required. The role may also be based in the United States, in Rahway or Upper Gwynedd. Only U.S.-based local candidates will be considered for U.S.-based positions, and no visa or relocation support to the United States will be provided. ++++++++++++++++++++++++++++++++++++ US and Puerto Rico Residents Only: Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process. As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics. As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit: EEOC Know Your Rights EEOC GINA Supplement We are proud to be a company that embraces the value of bringing together, talented, and committed people with varied experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with varied ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively. Learn more about your rights, including under California, Colorado and other US State Acts U.S. Hybrid Work Model Effective September 5, 2023, employees in office-based positions in the U.S. will be working a Hybrid work consisting of three total days on-site per week, Monday - Thursday, although the specific days may vary by site or organization, with Friday designated as a remote-working day, unless business critical tasks require an on-site presence. This Hybrid work model does not apply to, and daily in-person attendance is required for, field-based positions; facility-based, manufacturing-based, or research-based positions where the work to be performed is located at a Company site; positions covered by a collective-bargaining agreement (unless the agreement provides for hybrid work); or any other position for which the Company has determined the job requirements cannot be reasonably met working remotely. Please note, this Hybrid work model guidance also does not apply to roles that have been designated as “remote”. The salary range for this role is $190,800.00 - $300,300.00 This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employee’s position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs. The successful candidate will be eligible for annual bonus and long-term incentive, if applicable. We offer a comprehensive package of benefits. Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days. More information about benefits is available on our US Compensation and Benefits homepage. You can apply for this role through career page , (or via the Workday Jobs Hub if you are a current employee). The application deadline for this position is stated on this posting. San Francisco Residents Only: We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance Los Angeles Residents Only: We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles’ Fair Chance Initiative for Hiring Ordinance Search Firm Representatives Please Read Carefully We do not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails. Required Skills: Commercial Strategies, Cross-Functional Leadership, Data-Driven Decision Making, Executive Communications, Infectious Disease, Influence, Launch Excellence, Portfolio Management, Profit and Loss (P&L), Strategic Thinking Preferred Skills: Current Employees apply HERE Current Contingent Workers apply HERE Search Firm Representatives Please Read Carefully Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails. Employee Status: Regular Relocation: International VISA Sponsorship: Yes Travel Requirements: 50% Flexible Work Arrangements: Hybrid Shift: Not Indicated Valid Driving License: No Hazardous Material(s): no Job Posting End Date: 07/20/2026 *A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date. Our company is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where we have codified our legacy for over a century. Our success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare.

Business Intelligence
Data Analysis
Audit Data Analytics
Direct Apply
Posted 28 days ago
MSD

Associate Director, Global Clinical Supply Compliance (Hybrid)

MSDRahway, New JerseyFull-time
View Job
Compensation$90K - 130K a year

Lead global clinical supply quality systems ensuring compliant, inspection-ready operations and drive compliance strategy across stakeholders. | Bachelor's or Master's degree with 6+ years in regulated GxP environment managing quality systems globally. | Job Description The Associate Director in Global Clinical Supply (GCS) Compliance is a subject matter expert and project leader responsible for advancing and sustaining GxP Quality Systems across GCS to ensure clinical supply operations are executed in a compliant, inspection‑ready, and risk‑based manner. GCS supports Phase I–IV trials across 60+ countries in alignment with local and regional regulations for GxP (GMP, GDP, and GCP) and Environmental Health & Safety (EHS). In this role, the Associate Director applies deep technical judgment and systems level thinking to complex compliance challenges while influencing outcomes across a highly matrixed organization. This role provides expert support and project leadership for key GCS compliance processes —including deviations, CAPA, change control, documentation, training, audits/inspections, analytics, risk management, and EHS. Associate Directors are expected to apply expertise and subject matter depth broadly across these domains. The Associate Director partners closely with GCS functional areas and stakeholders within Development Sciences and Clinical Supply, our company's Research Laboratories Quality Assurance, Global Development Quality, IT/Digital, GCTO, Procurement, and other enterprise stakeholders to drive compliance strategy, QMS alignment, and performance improvement within GCS. Qualifications Education & Experience: Bachelor’s degree in a Scientific, Engineering, or related field with 8+ years of relevant experience in a regulated GxP environment; or master’s degree with 6+ years of experience in compliance, quality, technical operations, or related disciplines. Demonstrated experience in supporting or managing multiple GxP Quality Systems (e.g., deviations, CAPA, change control, documentation, training, audits/inspections, risk management, EHS) is required. Proven ability to lead cross-functional initiatives or complex compliance projects at a regional or global scale. Skill-based Qualifications: With strong subject matter expertise, sound judgment, and the ability to lead complex system and process design and execution, candidates must demonstrate: Experience and ability to provide technical oversight and strategic process leadership across multiple compliance pillars such as deviations, CAPA, change control, documentation, training, risk management, inspection/audit coordination, and Environmental Health & Safety. Proven track record of interpreting regulations and designing new processes or governance frameworks to drive compliance across global network. Includes ability to independently resolve complex compliance challenges and deliver sustainable improvements. Advanced ability to apply GxP and ALCOA+ principles to ensure quality and data integrity in system and process execution. Expertise in proactively identifying, assessing, and mitigating risks to timelines, scope, compliance outcomes, or deliverables, including high-level escalation and risk communication. Proficiency in performing and overseeing complex investigations and CAPA activities with deep root cause identification and QRM-aligned rigor. Ability to build and lead strong, trust‑based partnerships across Quality, Supply Chain, Technical Operations, IT, and clinical development stakeholders, enabling collaborative compliance strategies and performance improvement initiatives Exceptional analytical skills with demonstrated capability to interpret operational trends and support data‑driven decisions. Includes designing, implementing and optimizing data analytic tools or dashboards for actionable insights. Excellent communication skills, supporting clear, concise, and influential interactions across functional and site teams. Includes effective presentations of compliance findings and recommendations to leadership and key stakeholders. Preferred Experience and Skills: Working knowledge of Quality Risk Management (QRM) tools and concepts for application to investigations, change control, and system design. Experience contributing to or co‑leading Communities of Practice or SME networks. Experience supporting or leading Change Management activities (training, documentation updates, rollout planning). Experience with GMP electronic systems (e.g., MEDs, Veeva, TrackWise, LMS, SAP). Experience applying Lean Six Sigma or continuous improvement methodologies. #GCScareer #eligibleforERP #PSCS Required Skills: CAPA Management, Clinical Supply Chain Management, Communications Support, Compliance Strategies, Continuous Improvement, Data Integrity, Driving Continuous Improvement, GMP Compliance, Meeting Leadership, Quality Risk Assessment, Supply Chain Optimization Preferred Skills: Current Employees apply HERE Current Contingent Workers apply HERE US and Puerto Rico Residents Only: Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process. As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics. As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit: EEOC Know Your Rights EEOC GINA Supplement We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively. Learn more about your rights, including under California, Colorado and other US State Acts The salary range for this role is $129,000.00 - $203,100.00 This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employee’s position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs. The successful candidate will be eligible for annual bonus and long-term incentive, if applicable. We offer a comprehensive package of benefits. Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days. More information about benefits is available at https://jobs.merck.com/us/en/compensation-and-benefits. You can apply for this role through https://jobs.merck.com/us/en (or via the Workday Jobs Hub if you are a current employee). The application deadline for this position is stated on this posting. San Francisco Residents Only: We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance Los Angeles Residents Only: We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles’ Fair Chance Initiative for Hiring Ordinance Search Firm Representatives Please Read Carefully Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails. Employee Status: Regular Relocation: No relocation VISA Sponsorship: No Travel Requirements: 10% Flexible Work Arrangements: Hybrid Shift: 1st - Day Valid Driving License: No Hazardous Material(s): n/a Job Posting End Date: 07/9/2026 *A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date. Our company is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where we have codified our legacy for over a century. Our success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare.

GMP Compliance
Supply Chain Optimization
CAPA Management
Direct Apply
Posted 30 days ago
MSD

Procurement Specialist, Data Analyst & Support (Remote)

MSDAnywhereFull-time
View Job
Compensation$Not specified

| Job Description Role Summary We are seeking a detail-oriented Procurement Specialist to join our Global Capital Procurement (GCP) team. This role is pivotal in providing operational support and ensuring the smooth functioning of our procurement processes. Reporting to the Global Capital Procurement PMO Lead, the Specialist will collaborate closely with Regional Capital Procurement Execution teams, Global Capital Procurement Category teams, and various internal and external stakeholders to drive the success of our capital projects. The Specialist will serve as a system and process support lead, acting as a subject matter expert for our procurement tools, particularly SAP Ariba. This role involves providing comprehensive end-user and supplier support, managing procurement queues, and maintaining dashboards and data sets. The Specialist will also play a crucial role in standard management, process improvement, and compliance, ensuring that our teams adhere to updated guidelines and standards. Additionally, the Specialist will facilitate team coordination and communication, supporting onboarding processes, audits, and relevant communication efforts. The ideal candidate will be proactive and rigorous, data-literate, and capable of driving change to enhance efficiency and effectiveness within the procurement function. This position offers the flexibility of being either hybrid or remote, with teams based in US, Europe and Asia. Key Role Responsibilities1. System Support • Subject Matter Expertise: Serve as SME to the team and partners for all deployed Ariba modules, troubleshooting errors related to purchase orders, contracts, e-sourcing, and procure-to-pay processes • End-User and supplier Support: Provide comprehensive support for Ariba issues, inquiries, order routing, and RFP activities including training and vendor issue resolution • Queue Management: Monitor and manage procurement queues, review purchase orders, change orders and marketplace purchases, assist suppliers with PO and invoicing issues, manage expedited payment requirements per regulatory requirements • Contractor Invoice Management: Process purchase orders for contractors, support teams with time entry into CATS, troubleshoot system issues as needed • Tools and Systems: Provide support for emerging tools including project databases, Power BI dashboards, and digitized procurement processes; Represent the GCP team in future SAP module implementations and other system changes 2. Reporting and Data Analytics • Dashboard Management: update and maintain dashboards for monthly reviews, act as gate keeper on savings and coordinate entries into Ariba across teams and regions, manage reporting tier-1 and tier-2 impact spend, maintain GCP project tracker • Data Mining and Gap Analysis: conduct data mining and data conditioning for the teams, build ad-hoc reports with data extracted from existing systems, identify reporting gaps and develop and drive action plans • Support on Financial Reporting: help generate and maintain budget reports on actuals and forecast for procurement activities (contractor, travel expenses) 3. Standard Management and Process Improvement • GCP processes and guidelines: help team members in keeping guidelines and standards up to date, manage MEDS uploads and process database, drive schedule for process verification, action plan development, and guideline updates • Compliance: support the teams in understanding policy changes and updating working standards and guidelines • Audit Support: provide support for Corporate audits and other compliance inquiries 4. Team Coordination and Communication • SPOC Team Facilitation: facilitate weekly tactical calls with SPOCs and category teams as needed • Onboarding: support new employee onboarding processes, facilitate onboarding of contractors • Holiday Coverage: Provide SPOC backup support during absence Basic Qualifications • Required: Bachelor's degree or equivalent experience in supply chain procurement, business administration, Engineering, or a related field. • Desirable: Professional certification in procurement or supply chain management (e.g., CPSM, CPIM, CIPS) Experience • 3-5 years of experience in procurement, supply chain, or related business operations • Strong proficiency in SAP Ariba platform and modules • Experience with Qlik, Power BI, or similar business intelligence tools • Experience in process continuous improvement, project management and contract management • Knowledge of pharmaceutical or life sciences industry and Capital projects procurement practices Knowledge and skills • Procurement Expertise:Comprehensive knowledge of procurement practices, contract management, strategic sourcing, category management, and capital project lifecycle processes • Technology and Systems:Advanced proficiency in procurement software (SAP/Ariba platforms), ERP systems, MS Office Suite with advanced Excel capabilities, and digital collaboration tools (Teams, SharePoint, Power BI) • Data Analysis and Performance Management:Strong analytical skills with experience in data analysis, reporting, KPI measurement, and supplier performance evaluation • Communication and Stakeholder Management:Excellent verbal and written communication skills with the ability to present complex topics to diverse internal and external stakeholders, including suppliers and industry organizations • Cross-Functional Collaboration:Proven ability to work effectively across departments, regions, and time zones while influencing cross-functional leaders and supporting global teams • Systems Thinking and Process Optimization:Ability to understand complex procurement processes, drive continuous improvement, and optimize workflows for efficiency gains • Change Management and Problem-Solving:Capability to challenge current processes, solve complex problems, drive transformational changes, and lead improvement initiatives • Adaptability and Service Orientation:Flexibility to navigate dynamic, fast-paced environments with changing priorities while maintaining a customer service mindset • Attention to Detail and Organization:High level of detail-orientation with strong organizational skills and ability to deliver high-quality, timely outcomes • Sustainability and Inclusion Knowledge:Understanding of diversity/economic inclusion, environmental sustainability concepts, regulations, and industry best practices (desirable) Work Environment • This role is either remote or based at one of the large manufacturing sites. Required Skills: Adaptability, Adaptability, Biopharmaceutical Industry, Business Intelligence (BI), Capital Projects, Category Management, Clinical Supply Chain Management, Collaboration Tools, Contract Lifecycle Management (CLM), Contract Management, Cross-Functional Communications, Data Analysis, Driving Continuous Improvement, Inventory Control Management, Logistics, Microsoft Office, Onboarding, Procurement, Procurement Contracts, Procure-to-Pay, Production Planning, Project Management, Project Procurement Management, Purchasing Management, SAP Ariba {+ 5 more} Preferred Skills: Current Employees apply HERE Current Contingent Workers apply HERE US and Puerto Rico Residents Only: Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process. As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics.As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit: EEOC Know Your Rights EEOC GINA Supplement We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another's thinking and approach problems collectively. Learn more about your rights, including under California, Colorado and other US State Acts U.S. Hybrid Work Model Effective September 5, 2023, employees in office-based positions in the U.S. will be working a Hybrid work consisting of three total days on-site per week, Monday - Thursday, although the specific days may vary by site or organization, with Friday designated as a remote-working day, unless business critical tasks require an on-site presence.This Hybrid work model does not apply to, and daily in-person attendance is required for, field-based positions; facility-based, manufacturing-based, or research-based positions where the work to be performed is located at a Company site; positions covered by a collective-bargaining agreement (unless the agreement provides for hybrid work); or any other position for which the Company has determined the job requirements cannot be reasonably met working remotely. Please note, this Hybrid work model guidance also does not apply to roles that have been designated as "remote". The salary range for this role is $77,700.00 - $122,300.00 This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employee's position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs. The successful candidate will be eligible for annual bonus and long-term incentive, if applicable. We offer a comprehensive package of benefits. Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days. More information about benefits is available at https://jobs.merck.com/us/en/compensation-and-benefits. You can apply for this role through https://jobs.merck.com/us/en (or via the Workday Jobs Hub if you are a current employee). The application deadline for this position is stated on this posting. San Francisco Residents Only:We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance Los Angeles Residents Only:We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance Search Firm Representatives Please Read Carefully Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails. Employee Status: Regular Relocation: No relocation VISA Sponsorship: No Travel Requirements: 10% Flexible Work Arrangements: Remote Shift: Not Indicated Valid Driving License: No Hazardous Material(s): n/a Job Posting End Date: 10/17/2025 • A job posting is effective until 11:59:59PM on the day BEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.

Verified Source
Posted 10 months ago
MSD

Director, Animal Health - Customer Insights Lead

MSDAnywhereFull-time
View Job
Compensation$187K - 294K a year

Lead customer advisory boards and build strong customer relationships to inform R&D portfolio strategy and market activation efforts, ensuring alignment with customer needs and business goals. | 10+ years in large technology or biopharma organizations with leadership in customer insights, ability to influence cross-functional teams, strong analytical and communication skills, and experience driving organizational change. | Job Description The Customer Insights Lead is a strategic leader responsible for shaping and optimizing our Technology Solutions R&D portfolio and Market Activation efforts in alignment with customer needs and the organization’s business objectives. This person will lead a customer-facing role, responsible for elevating our organization’s understanding of customers’ operations to generate a comprehensive and proprietary customer knowledge base that will be leveraged as a key source of competitive advantage for our Technology Solutions business. He/she will build strong relationships with some of our largest and most influential customers, recruiting them to become our partners during the new product development process, as well as product champions once these new solutions reach launch stage. The Customer Insights Lead will organize and lead four to five Customer Advisory Boards (CABs) across multiple livestock segments and will be tasked with synthesizing CAB insights to ensure that business decisions are grounded in a sophisticated understanding of market opportunities, customer pain points, and emerging industry trends. Through CABs, he/she will leverage customer insights to guide our R&D pipeline strategy towards delivering innovative and differentiated solutions that maximize portfolio ROI. Finally, the Customer Insights Lead will leverage this unique knowledge base to guide Market Activation initiatives and maximize our technology portfolio’s commercial performance. As a key player in the organization, the Customer Insights Lead will be part of the Technology Design & Customer Interface (TDCI) Leadership Team and manage a significant budget dedicated to drive Technology Solutions towards ambitious revenue targets and commitments to our company's Animal Health (MAH). Key Responsibilities Customer Insights Champion: Champion a customer-centric culture and lead a global initiative to elevate our understanding of customer needs and market opportunities to inform strategic analysis and drive critical decision-making processes. • Lead, design, and launch four or more CABs comprised by select, highly influential, key account customers, defining membership, objectives, and engagement strategies. • Work closely with Regional Vice-Presidents and Country Managers to identify key customers and opinion leaders across key global markets with significant market potential. • Lead the process of recruiting key customers to join CABs and to become close partners during the new product development process, ensuring our solutions are designed around customer needs. • Facilitate annual CAB in-person meetings for each business segment as well as frequent virtual workshops and roundtable discussion to engage customers and ensure the capture of rich and diverse perspectives. • Build strong relationships with CAB executive members throughout this process so they evolve organically into product champions that promote our solutions to expand penetration and maximize sales outcomes. • Distill CAB discussions into strategic recommendations and share outcomes with MAH Executive Leadership Team, R&D, and commercial teams. • Continuously evaluate and improve CAB effectiveness through feedback, performance metrics, and best practices. • Create and maintain a dynamic customer needs repository, ensuring the organization remains aware and responsive to evolving market demands. Portfolio Strategy Leadership: Develop comprehensive R&D portfolio management strategy for Technology Solutions, ensuring roadmaps across species and business segments align with customer needs and strategic priorities. • Lead multi-disciplinary teams towards creating clearly articulated customer value propositions for our technology solutions and correlate these to revenue projections for our innovative products and R&D pipeline. • Build comprehensive analytical models to quantify market potentials and revenue projections within an evidence-based framework and ensure that framework is leveraged consistently across R&D projects. • Lead governance forums and facilitate transparent, data-driven decision-making for pipeline investments, resource allocation, and program prioritization. • Connect TDCI strategies to the overall MAH strategic framework and work closely with the “Tech Adoption Strategic Pillar” Lead to make sure our metrics are aligned with business goals and 5YP targets as set by the MAH’s Executive Vice-President and Leadership Team. Market Activation Excellence: Leverage customer knowledge base and expertise to lead cross-portfolio Market Activation initiatives and maximize portfolio sales performance. • Coordinate New Product Launch activities across species and business segments ensuring strategy execution includes CAB executive members as Product Champions. • Partner with TDCI Leads to develop go-to-market strategies that effectively communicate product’s customer value proposition to maximize financial outcomes. • Establish clear connections between TDCI roadmap projects across species and business segments and 5YP targets to drive sales budgeting processes. • Build strong rapport with Regional and Local Operations to effectively activate and execute joint commercial initiatives towards maximizing sales performance of our current portfolio. Experience and Skills • Unapologetic Customer Champion: Proven leadership presence required to ensure customer needs become central to strategy and roadmap decisions at the highest governance levels. • Influence & Impact: Skilled in translating customer voice into strategic action and driving organizational alignment. • Collaboration: Effective working within cross-disciplinary teams and managing competing priorities; ability to lead without direct authority. • Analytical Rigor: Strong ability to interpret complex data and derive actionable insights; proficiency in financial modelling and scenario planning. • Communication: Adept at tailoring messages to diverse audiences, from technical teams to executive leadership. • Relationship Building: Proven capability to cultivate trust and rapport with external customers and internal teams. • Commercial Acumen: Experienced in developing go-to-market strategies focused on business and commercial solutions. • Agility: Comfortable navigating ambiguity and adapting to rapidly changing environments. • Cultural Intelligence: Capable of navigating diverse cultural norms and values to effectively lead global teams. This is a remote position that can be based in multiple regions. Education: • Bachelor's degree in related area of study. Required: • 10+ years of experience large technology and/or biopharma corporate organizations. • Positive attitude, excellent interpersonal skills, and proven ability to navigate highly matrixed organizations. • Exceptional attention to detail and commercial instinct. • Veterinary training and technical background in livestock are preferred. • Proven leadership in driving organizational change and continuous improvement. • Ability to travel 30 to 40% of the time. • Given the global nature of the role, fluency in English is required; ability to speak additional languages is desired. #MSJR Current Employees apply HERE Current Contingent Workers apply HERE US and Puerto Rico Residents Only: Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process. As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics. As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit: EEOC Know Your Rights EEOC GINA Supplement​ We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively. Learn more about your rights, including under California, Colorado and other US State Acts U.S. Hybrid Work Model Effective September 5, 2023, employees in office-based positions in the U.S. will be working a Hybrid work consisting of three total days on-site per week, Monday - Thursday, although the specific days may vary by site or organization, with Friday designated as a remote-working day, unless business critical tasks require an on-site presence.This Hybrid work model does not apply to, and daily in-person attendance is required for, field-based positions; facility-based, manufacturing-based, or research-based positions where the work to be performed is located at a Company site; positions covered by a collective-bargaining agreement (unless the agreement provides for hybrid work); or any other position for which the Company has determined the job requirements cannot be reasonably met working remotely. Please note, this Hybrid work model guidance also does not apply to roles that have been designated as “remote”. The salary range for this role is $187,000.00 - $294,400.00 This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employee’s position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs. The successful candidate will be eligible for annual bonus and long-term incentive, if applicable. We offer a comprehensive package of benefits. Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days. More information about benefits is available at https://jobs.merck.com/us/en/compensation-and-benefits. You can apply for this role through https://jobs.merck.com/us/en (or via the Workday Jobs Hub if you are a current employee). The application deadline for this position is stated on this posting. San Francisco Residents Only: We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance Los Angeles Residents Only: We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles’ Fair Chance Initiative for Hiring Ordinance Search Firm Representatives Please Read Carefully Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails. Employee Status: Regular Relocation: No relocation VISA Sponsorship: Yes Travel Requirements: 50% Flexible Work Arrangements: Remote Shift: Not Indicated Valid Driving License: No Hazardous Material(s): N/A Required Skills: Biopharmaceutical Industry, Biopharmaceutical Industry, Business Decisions, Commercial Excellence, Content Marketing, Cross-Cultural Awareness, Cultural Intelligence, Customer Insights, Customer Relationship Building, Customer Value Proposition Development, Digital Marketing, Global Team Collaboration, Go-to-Market Strategies, Livestock Management, Market Development, Marketing Communications Planning, Market Research, Organizational Alignment, People Leadership, Portfolio Management, Pricing Strategies, Professional Networking, Relationship Building, Results-Oriented, Strategic Thinking {+ 1 more} Preferred Skills: Job Posting End Date: 10/6/2025 • A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.

Customer Insights
Leadership
Innovation
New Product Development
Market Research
Consumer Insights
Strategic Planning
Portfolio Management
Relationship Building
Cross-Cultural Awareness
Go-to-Market Strategies
Commercial Acumen
Analytical Rigor
Cultural Intelligence
Verified Source
Posted 10 months ago
MS

US Strategy Lead Director Medical Affairs (USDMA)/ Rheumatology & Dermatology (Remote)

MSDAnywhereFull-time
View Job
Compensation$187K - 294K a year

Lead and execute US medical affairs strategies for rheumatology and dermatology, drive scientific excellence, coordinate field readiness, manage training and advisory boards, and collaborate cross-functionally to align with global and regional goals. | Advanced degree (MD) with 5+ years medical affairs experience, 3+ years in relevant therapeutic area, strategic decision-making skills, strong communication, knowledge of US healthcare system, and ability to travel up to 40%. | Job Description Role Summary The US Director Medical Affairs (USDMA) is a regionally based position within our Company Research Laboratories, US Medical Affairs (our Research and Development Division USMA), and is a US Country Level Strategic director focusing on Rheumatology & Dermatology. This position strategically drives scientific excellence across in-line business and the One Company's Pipeline while optimizing field readiness across the USMA strategic pillars: Scientific Exchange Company Trials Investigator-Sponsored Programs Congresses Insights The US DMA is an experienced therapeutic area (TA) leader and subject matter expert (SME) with relevant medical affairs and field medical experience. This role is also responsible for driving execution of scientific and medical affairs plans for assigned Therapy Areas within their region, engaging with regional cross-functional teams, and providing US input to the relevant cross-functional team meetings, e.g., US MAT, PAT, MT and V&I Plans. As a core member (or co-lead) of the US Medical Affairs Team (MAT), the US DMA collaborates with the Global TA team and cross-functional partners to enable US regional implementation of Value & Implementation (V&I) Planning by: Integrating local insights into Global Scientific Value Content (GSVC) and Center of Scientific Exchange Excellence (CSEE) plans Facilitating local adoption of GSVC and CSEE initiatives Leading development and execution of aligned local training programs Evaluating training effectiveness and application in the field. Primary Responsibilities In collaboration with USMA Executive Director (ED) and Health Systems Payor Access Strategy Lead (PASL), conduct development and implementation of regional strategies aligned with headquarters V&I goals including defining a prioritized USMA Field strategy and implementation goals. Contribute to the integrated US Country Medical Affairs Plan (CMAP), including the US Field Medical Plan (FMP)/Field Engagement Plan (FEP) and field training plan for assigned TA as a member of the USMA TA Leadership Team Identifies and prioritizes US field resources, training needs and activities; and in collaboration with GMVC, ensures strategically aligned content and training and any other needed adult learning activities across the portfolio. This would also include the pull-through of pre- and post-congress regional training and content. Develop a strategic and comprehensive scientific engagement plan and ensure scientific exchange aligns with the global scientific communications platform. Ensure insights from advisory boards and field medical activities are actioned with relevant stakeholders, aligned with Country Medical Affairs priorities, and monitored for trends impacting future strategy. In collaboration with relevant USMA stakeholders (e.g. HS PASL), organize expert input events (e.g., advisory boards, forums) with contracted Scientific Leaders and key stakeholders to address new indication implementation and/or emerging science. Manage programs (i.e. patient support, education, risk management) as needed for appropriate and safe utilization of company medicines. Partner with GSVC, CSEE, US Global Clinical Trial Organization (GCTO), Global Medical and Scientific Affairs (GMSA) TA leads, and internal/external SMEs to orchestrate and deliver regional training as needed. Participate in bi-directional information exchange and sharing of best practices across USMA roles and teams, including Health Systems. Collaborate with the USMA Field Medical Alignment Director (FMAD) to ensure consistent standards, processes, and harmonization for training activities (e.g., clinical immersions, verbalizations, journal clubs). Provide input into strategic congress priorities and participate in planning at key scientific congresses. Continuously monitor healthcare environment and emerging trends to optimize CMAPs and field execution plans. Additional Responsibilities (as applicable) Serve as a point of contact for development and maintenance of US new-hire scientific foundational onboarding in collaboration with leadership and SMEs. Work with USMA Leadership and GMVC stakeholders to ensure consistent verbalization processes for new hires and tenured RMSDs regarding new data, indications, and disease areas. Provide support for the Investigator Studies Program (ISP) for assigned TA, including Areas of Interest consultation, dissemination, data highlights, training, and scientific review as requested by the GMSA ED. Required Qualifications, Skills & Experience An advanced degree (e.g., MD, PhD, PharmD) relevant to the TA-specific disease area and recognized medical expertise in the TA (rheumatology) A minimum of 5 years of medical affairs experience or equivalent clinical/research experience A minimum of 3 years of working in therapeutic area (clinical, research, or pharmaceutical environment) or within a highly relevant TA with demonstrated scientific acumen Proven ability in Strategic Decision Making & Planning, including helping the US Executive Director prioritize initiatives across the portfolio. Demonstrated Execution Excellence with a track record of leading complex projects, managing multiple priorities simultaneously in a fast-paced environment. Strong Emotional Intelligence to foster trust and respect within a complex, matrixed organizational structure. Exceptional Networking & Partnerships skills to collaborate effectively across diverse teams and stakeholders. Agile mindset as a Change Catalyst, committed to experimenting, learning, and adapting in response to evolving business needs, and capable of driving continuous improvement. Expertise in interpreting and communicating complex scientific concepts clearly in both one-on-one and group settings. Deep knowledge of the US healthcare system, including national treatment guidelines, clinical research processes, FDA regulations, and OIG compliance. The ability to travel up to 40% (i.e.: Congresses) Preferred Qualifications: Field Medical Affairs experience. University-level teaching experience and understanding of adult learning principles. Experience with innovative pharmaceutical training platforms. Proficiency in Microsoft Word, PowerPoint, and Excel. Ability to quickly assimilate new subject areas and work independently on complex problems #eligibleforERP Current Employees apply HERE Current Contingent Workers apply HERE US and Puerto Rico Residents Only: Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process. As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics. As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit: EEOC Know Your Rights EEOC GINA Supplement We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively. Learn more about your rights, including under California, Colorado and other US State Acts U.S. Hybrid Work Model Effective September 5, 2023, employees in office-based positions in the U.S. will be working a Hybrid work consisting of three total days on-site per week, Monday - Thursday, although the specific days may vary by site or organization, with Friday designated as a remote-working day, unless business critical tasks require an on-site presence.This Hybrid work model does not apply to, and daily in-person attendance is required for, field-based positions; facility-based, manufacturing-based, or research-based positions where the work to be performed is located at a Company site; positions covered by a collective-bargaining agreement (unless the agreement provides for hybrid work); or any other position for which the Company has determined the job requirements cannot be reasonably met working remotely. Please note, this Hybrid work model guidance also does not apply to roles that have been designated as “remote”. The salary range for this role is $187,000.00 - $294,400.00 This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employee’s position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs. The successful candidate will be eligible for annual bonus and long-term incentive, if applicable. We offer a comprehensive package of benefits. Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days. More information about benefits is available at https://jobs.merck.com/us/en/compensation-and-benefits. You can apply for this role through https://jobs.merck.com/us/en (or via the Workday Jobs Hub if you are a current employee). The application deadline for this position is stated on this posting. San Francisco Residents Only: We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance Los Angeles Residents Only: We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles’ Fair Chance Initiative for Hiring Ordinance Search Firm Representatives Please Read Carefully Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails. Employee Status: Regular Relocation: No relocation VISA Sponsorship: No Travel Requirements: 50% Flexible Work Arrangements: Remote Shift: Not Indicated Valid Driving License: No Hazardous Material(s): n/a Required Skills: Clinical Research, Communication, External Collaboration, Investigator-Initiated Studies (IIS), Medical Affairs, Pharmaceutical Medical Affairs, Pharmacoeconomics, Professional Networking, Rheumatology, Strategic Planning, Strategic Thinking Preferred Skills: Job Posting End Date: 10/11/2025 *A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date. Our company is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where we have codified our legacy for over a century. Our success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare.

Medical Affairs
Clinical Research
Strategic Planning
Communication
External Collaboration
Investigator-Initiated Studies
Pharmaceutical Medical Affairs
Pharmacoeconomics
Professional Networking
Rheumatology
Direct Apply
Posted 11 months ago
MS

Platform Engineer (Specialist) – Cybersecurity Automation & AI (Remote)

MSDAnywhereFull-time
View Job
Compensation$78K - 122K a year

You will build workflows that integrate across various security platforms, enabling automation pipelines that support AI-driven defense. This role requires understanding platform capabilities and shaping secure automation patterns that scale. | Candidates should have 1-2 years of experience in security engineering or IT automation, with proficiency in scripting languages like Python and PowerShell. A strong understanding of cybersecurity fundamentals and experience with enterprise platforms is essential. | Job Description Position Summary: We are hiring a Platform Engineer to join the Cybersecurity Automation & AI team. This is not a traditional automation role—you will help design and deliver the next generation of cybersecurity systems through secure, intelligent automation. You will build workflows that integrate across Microsoft Defender XDR, Sentinel, ServiceNow, and other enterprise platforms, enabling automation pipelines that support AI-driven defense and enterprise-scale risk reduction. Job Description: You’ll be working in a forward-leaning engineering function focused on transforming how cybersecurity operates—less detection, more design. The systems you build will be foundational to how we scale AI, automate risk response, and reduce manual toil across the enterprise. As a Platform Engineer, you’ll support the development of cross-platform cybersecurity automation workflows under the direction of the Platform Engineering Lead. You will be expected to go beyond implementation—to understand platform capabilities, evaluate extensibility, and help shape secure automation patterns that scale. This role requires working knowledge of cybersecurity—not just scripting or tool familiarity. You must understand why specific workflows exist (e.g., identity verification, privilege revocation, endpoint containment), what constitutes a secure pattern, and how your automation affects broader enterprise risk posture. You won’t own the tools—but you must deeply understand how to interact with them via APIs, orchestration frameworks, and platform-native automation features. Key Responsibilities: Build and support automation workflows across security platforms such as ServiceNow, Defender XDR, and Sentinel. Learn and apply platform-native capabilities, APIs, and extensibility models to solve real-world security automation challenges. Contribute to orchestration logic that includes trigger conditions, telemetry tagging, enrichment, and response actions. Implement automation scripts and integrations using Python, PowerShell, and REST APIs. Participate in test planning, safety validation, change control, and rollback design. Document technical implementations, integration patterns, and decision logic. Collaborate with engineers and domain owners to identify automation opportunities. Apply cybersecurity understanding to ensure automation is relevant, secure, and impactful. Required Qualifications: 1–2 years of hands-on experience in security engineering, IT automation, or platform integration; candidates with strong project-based or adjacent technical experience will be considered Experience with at least one enterprise platform such as Microsoft Defender, Sentinel, or ServiceNow Proficient in scripting (Python, PowerShell) and building workflows using REST APIs Strong understanding of cybersecurity fundamentals (e.g., least privilege, threat response, asset visibility, risk signals) Ability to translate security goals into platform-appropriate automation Comfortable operating in a federated environment where tools are not owned directly Preferred Qualifications: Experience with ServiceNow Flow Designer or IntegrationHub Exposure to multiple cybersecurity domains such as IAM, endpoint protection, or SIEM Experience building automation in large, regulated environments Familiarity with kill switch design, governance, and rollback in automation workflows Clear documentation and collaboration skills across cross-functional engineering teams Current Employees apply HERE Current Contingent Workers apply HERE US and Puerto Rico Residents Only: Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process. As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics. As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit: EEOC Know Your Rights EEOC GINA Supplement We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively. Learn more about your rights, including under California, Colorado and other US State Acts U.S. Hybrid Work Model Effective September 5, 2023, employees in office-based positions in the U.S. will be working a Hybrid work consisting of three total days on-site per week, Monday - Thursday, although the specific days may vary by site or organization, with Friday designated as a remote-working day, unless business critical tasks require an on-site presence.This Hybrid work model does not apply to, and daily in-person attendance is required for, field-based positions; facility-based, manufacturing-based, or research-based positions where the work to be performed is located at a Company site; positions covered by a collective-bargaining agreement (unless the agreement provides for hybrid work); or any other position for which the Company has determined the job requirements cannot be reasonably met working remotely. Please note, this Hybrid work model guidance also does not apply to roles that have been designated as “remote”. The salary range for this role is $77,700.00 - $122,300.00 This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employee’s position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs. The successful candidate will be eligible for annual bonus and long-term incentive, if applicable. We offer a comprehensive package of benefits. Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days. More information about benefits is available at https://jobs.merck.com/us/en/compensation-and-benefits. You can apply for this role through https://jobs.merck.com/us/en (or via the Workday Jobs Hub if you are a current employee). The application deadline for this position is stated on this posting. San Francisco Residents Only: We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance Los Angeles Residents Only: We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles’ Fair Chance Initiative for Hiring Ordinance Search Firm Representatives Please Read Carefully Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails. Employee Status: Regular Relocation: VISA Sponsorship: Travel Requirements: Flexible Work Arrangements: Remote Shift: Valid Driving License: Hazardous Material(s): Required Skills: Design Applications, Information Security, Security Operations, SLA Management, Software Development, Software Development Life Cycle (SDLC), System Designs, Technical Advice, Vulnerability Scanning Preferred Skills: Job Posting End Date: 08/5/2025 *A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date. Our company is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where we have codified our legacy for over a century. Our success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare.

Cybersecurity
Automation
Scripting
APIs
Integration
Documentation
Collaboration
Risk Management
Orchestration
Python
PowerShell
ServiceNow
Microsoft Defender
Sentinel
Security Engineering
Workflow Design
Direct Apply
Posted about 1 year ago

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