Roche

Lead the design and implementation of complex mechanical systems supporting research laboratories and vivarium environments, ensuring safety, reliability, and compliance. | Bachelor's in Mechanical Engineering with 15+ years in pharmaceutical or related industries, extensive experience in mechanical design, construction, commissioning, and industry standards. | Genentech is establishing a new Campus Development Team (CDT) to oversee the implementation of the Campus Vision Plan (CVP) for the South San Francisco campus. This Senior Principal Mechanical Engineer position provides single-point accountability for the successful end-to-end delivery of all Mechanical systems, with a primary focus on the complex laboratory and research environments within the gRED development. This role will also provide expertise for the supporting Vivarium, Utility Plant, and Electrical Distribution Hub as part of the CVP. The Principal Mechanical Engineer works within a large, cross-functional project organization and serves as the primary technical liaison, coordinating the specific mechanical systems (HVAC, plumbing, fire protection, building controls, automation and energy management) and reliability needs of scientific and vivarium user groups into actionable engineering designs. This position is responsible for ensuring all mechanical systems are delivered safely, on schedule, within budget, and to the highest standards of quality, meeting the critical demands of a world-class R&D and animal care facility. The Opportunity Responsibilities: The responsibilities for this position may include, but are not limited to: ● Provides technical leadership and deep subject matter expertise for the mechanical engineering designs supporting gRED research laboratories, specialized vivarium spaces, and associated supporting projects. ● Actively leads the design and planning of HVAC, plumbing, fire protection, building controls, automation and energy management critical to laboratory operations and specialized vivarium environments. ● Coordinates with the Utility Master Plans to ensure that upgrades to critical mechanical infrastructure (including the Regional Utility Plant and Electrical Distribution Hub) directly support the reliability, redundancy and scalability required by the new lab facilities. ● Serves as a respected industry expert on laboratory mechanical design, engaging with the Roche/Genentech internal and industry external network to learn, influence, and collaborate on new technologies and best practices for gRED. ● Primary focus will be ensuring scientific user requirements are incorporated into robust technical solutions for the gRED project. ● Provide expert design guidance on HVAC, plumbing, fire protection, building controls, automation and energy management to labs and strategies for flexible 'plug-and-play' capabilities, and robust back-up systems to protect critical experiments, data, and animal life-support systems. ● Work closely with other technical leads to ensure seamless integration of HVAC, plumbing, fire protection, building controls, automation and energy management systems with lab-specific platforms like Building Automation Systems (BAS) and environmental monitoring systems. ● Serve as the mechanical SME in all design and user-group meetings, providing clear technical options analysis and advocating for designs that prioritize scientific workflow, flexibility, and safety. ● A key function of this role will also be to ensure all mechanical designs align with Roche/Genentech and site-specific standards, with a particular focus on standards governing laboratory design and vivarium operations. ● Coordinates the mechanical scope into a comprehensive strategy to address the technical needs across all aspects of the gRED project, from main infrastructure to the point-of-use in the lab. ● A portion of the Principal Mechanical Engineer’s time will be spent supporting broad Design Engineering & Construction Services process improvement projects and LEAN initiatives, applying these principles to improve the lab design and delivery process. ● The Senior Principal Mechanical Engineer will be responsible for driving innovation in mechanical systems specifically for R&D environments, adopting technologies that improve lab flexibility, energy efficiency, and operational reliability. ● This role will participate in the development of a project-wide mechanical infrastructure strategy, in partnership with the Design team, to ensure the new gRED labs are adaptable for future scientific platforms and technologies, reducing total cost of ownership while maximizing uptime and research continuity. ● A key portion of the role is continuous learning, engagement with the Roche engineering network (technical experts within the Roche Global organization and other Roche sites) as well as outside industry organizations, including ASHRAE, ISPE and others. Key Tasks: ● Project Planning and Coordination: Develop and maintain a comprehensive project plan, coordinating with architects, engineers, and contractors. Apply innovative thinking to proactively identify and mitigate risks, while monitoring progress via KPIs and reporting status to senior management. ● Budgeting and Resource Management: Support the development and management of the project budget, ensuring cost control and effective resource allocation. This role also supports all procurement activities, including vendor selection, contract negotiation, and material acquisitions. ● Stakeholder Management: Build and maintain strong relationships with internal and external stakeholders, fostering collaboration, transparency, and alignment. Serve as a trusted liaison, keeping all parties informed and engaged through regular meetings and progress reports. ● Team Leadership: Provide effective leadership by clarifying roles and fostering a collaborative, motivated work environment. Mentor and guide team members while also contributing strategic design and technical expertise to the facility's construction. ● Quality Control: Implement and enforce strict quality control measures to ensure compliance with industry standards and specifications.. Who You Are Requirements: ● Bachelor’s degree in Mechanical Engineering or equivalent. ● 15 years or more pharmaceutical technology experience in industry or academia after receiving their Bachelor’s Degree, at least 8 of which involved mechanical system design, construction and\or commissioning and qualification activities. ● Working knowledge of ANSI / ASHRAE, NEMA, NFPA, EPA, and OSHA standards as well as relevant chemical industry specific standards and documentation (piping and instrumentation diagrams, process flow diagrams). ● Pharmaceutical GMP project mechanical design experience, LEED certification, experience in project management, LEAN / Six Sigma certification, and/or experience working in a campus environment highly desired, but not required. ● Must have excellent communication (written/verbal), presentation, leadership, interpersonal, collaborative, conflict resolution, and negotiating skills ● Excellent organization and planning skills. ● Advanced Microsoft Office and Google Suite skills. ● Exceptional teamwork and collaboration skills are essential to facilitate the work of cross-functional and interdepartmental teams. ● Must be dependable, provide attention to details, and execute proficiently in coordination tasks. ● Self-starter and ability to work with minimum or no supervision. Relocation benefits are not available for this posting. The expected salary range for this position based on the primary location of California is $168,10000 - $312,300 USD Annual. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance. This position also qualifies for the benefits detailed at the link provided below. Benefits Genentech is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws. If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants. Who We Are Genentech, a member of the Roche group and founder of the biotechnology industry, is dedicated to pursuing groundbreaking science to discover and develop medicines for people with serious and life-threatening diseases. To solve the world's most complex health challenges, we ask bigger questions that challenge our industry and the boundaries of science to transform society. Our transformational discoveries include the first targeted antibody for cancer and the first medicine for primary progressive multiple sclerosis. The next step is yours. To apply today, click on the "Apply for this job" button. Genentech is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws. If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants.

Manage technical development teams and projects in pharmaceutical drug development from pre-entry into humans until launch, ensuring schedule adherence and risk mitigation. | Bachelor's degree in Life Sciences, 5 years pharmaceutical/biotech experience, 1-3 years drug development project management, PMP preferred, strong communication and collaboration skills. | Technical Development Team Project Manager The Technical Development Team Project Manager (TDT PM) partners with a Technical Development Leader (TDL) to manage technical development team(s) in defining and implementing CMC strategies and activities associated with developing clinical candidates from pre-entry into humans until launch. He/she provides project and process management experience including project planning and scheduling, resource forecasting, performance monitoring, and facilitation of communication and decision making to help drive assigned projects to a successful outcome. This position is based in South San Francisco, on site. The Opportunity You partner with the Technical Development Lead (TDL) and technical teams to define the CMC strategy and objectives for 3-5 projects across various platforms (large/small molecules, new modalities). Managing technical development teams (TDTs) and external partners (CMOs), applying project management expertise to establish integrated schedules, ensuring adherence to timelines, and proactively managing/reducing critical path risks. You drive key business processes for TDTs, including risk assessment, governance reviews, and the application of agile principles for efficient meetings and fast, focused decision-making. You effectively plan and facilitate TDT meetings, and ensure all relevant stakeholders are regularly updated on project status, risks, and issues. Participating in departmental initiatives, driving business process improvement, and acting as a valuable member of the Project Team System by sharing best practices and lessons learned. Who You Are (Required) B.S. degree in Life Sciences is required; advanced degree (M.S/PhD) is preferred. 5 years in the pharmaceutical/biotech industry. 1-3 years of drug development project management experience. PMP certification is preferred. Preferred Knowledge/Skills/Competencies Understanding of the drug development and CMC process development. Project management experience with a good understanding of PM practices, business processes and tools; relevant process validation, CMC functions, regulatory, quality and cGMP experience preferred. Strong desire to learn and expand CMC knowledge and digital technology advancement. Advocate and drive the digital transformation to project management. Excellent verbal and written communication skills; must be able to effectively communicate/articulate TDT strategy and deliverables to team members and external business partners. Strong collaborative and relationship-building skills; demonstrated ability to effectively partner and influence internal and external stakeholders. Relocation benefits are not available for this job posting. The expected salary range for this position based on the primary location of California is $91,100.00 - $150,000.00. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance. This position also qualifies for the benefits detailed at the link provided below. Benefits Genentech is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws. If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants. Who We Are Genentech, a member of the Roche group and founder of the biotechnology industry, is dedicated to pursuing groundbreaking science to discover and develop medicines for people with serious and life-threatening diseases. To solve the world's most complex health challenges, we ask bigger questions that challenge our industry and the boundaries of science to transform society. Our transformational discoveries include the first targeted antibody for cancer and the first medicine for primary progressive multiple sclerosis. The next step is yours. To apply today, click on the "Apply for this job" button. Genentech is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws. If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants.

Leading a large multidisciplinary team in computational biology for Oncology, setting strategy, and driving innovation to support drug discovery and development. | PhD in a scientific or technical field with 15+ years of experience, deep expertise in computational biology, proven leadership in large teams, and experience in pre-clinical and clinical Oncology research. | A healthier future. It’s what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. That’s what makes us Roche. Advances in AI, data, and computational sciences are transforming drug discovery and development. Roche’s Research and Early Development organisations at Genentech (gRED) and Pharma (pRED) have demonstrated how these technologies accelerate R&D, leveraging data and novel computational models to drive impact. Seamless data sharing and access to models across gRED and pRED are essential to maximising these opportunities. The new Computational Sciences Center of Excellence (CoE) is a strategic, unified group whose goal is to harness this transformative power of data and Artificial Intelligence (AI) to assist our scientists in both pRED and gRED to deliver more innovative and transformative medicines for patients worldwide. This role will ensure that gRED and pRED are supported and enabled with world-leading data, analytical, and computational biology approaches in Oncology while developing our projects through the pre-clinical and clinical stages. This role is a leader of leaders, leading teams with a broad scope of bioinformatics, biostatistics, specialised disease and data science expertise with a primary focus on Oncology. As the Executive Director of Computational Biology - Oncology, you lead a team developing innovative data analysis solutions for target identification, target assessment, disease understanding, molecule characterization (mode of action, safety, etc.), improving predictive validity of pre-clinical models as well as supporting clinical development strategies by characterizing patient populations and identifying biomarker candidates. You drive impact on the gRED and pRED portfolio, build strong stakeholder relationships, and set strategy for your team and Roche. Your responsibilities include making decisions on talent, resourcing, business processes, and capability development, contributing to the organization's overall success. The Opportunity: Strategic leadership of the Computational Biology - Oncology department within Computational Center of Excellence and member of the Computational Biology and Medicine LT Define vision and strategy for computational biology in Oncology to achieve gRED and pRED objectives and implement world-leading approaches in portfolio projects to identify and assess new targets and to support the characterization of molecules and models that inform data driven decisions along the value chain. Responsible for hiring, developing, and retaining talent, fostering an environment for team members to broaden their skills for enhanced outcomes Ensure standardized tools and pipelines for computational biology, collaborating closely with biologists and computational leaders for efficient data flow and decision-making Drive innovation in analysis approaches, establish strong internal and external partnerships, and lead by example to demonstrate and align with our core values Who You Are: PhD in a scientific or technical field with 15+ years of experience, including significant group management and team formation Deep expertise in computational biology, bioinformatics, biostatistics, data science, or similar fields Proven expertise in pre-clinical and clinical research in Oncology. Proven experience leading large teams, involving multiple stakeholders, and achieving outstanding results efficiently Excellent partnering and collaboration skills, building trustful partnerships with internal and external stakeholders Deep understanding of how biological data analysis impacts decision-making along the value chain Ability to lead a multidisciplinary team, quickly understand topics, formulate problem statements, and achieve successful outcomes Willingness to travel regularly to ensure exchange with your global team members and stakeholders. Thrives in ambiguity, identifying opportunities, and bringing clarity to the team while fostering a growth mindset and development opportunities for direct reports. Relocation benefits are available for this job posting. This role will be based in the South San Francisco or Basel campus and onsite presence is expected. The expected salary range for this position based on the primary location of California is $249,600 - $463,500. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance. This position also qualifies for the benefits detailed at the link provided below. Benefits #LI-JD1 #ComputationCoE Genentech is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws. If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants. Who We Are Genentech, a member of the Roche group and founder of the biotechnology industry, is dedicated to pursuing groundbreaking science to discover and develop medicines for people with serious and life-threatening diseases. To solve the world's most complex health challenges, we ask bigger questions that challenge our industry and the boundaries of science to transform society. Our transformational discoveries include the first targeted antibody for cancer and the first medicine for primary progressive multiple sclerosis. The next step is yours. To apply today, click on the "Apply for this job" button. Genentech is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws. If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants.

Manage and grow strategic accounts by fostering relationships, developing strategic plans, and delivering tailored solutions. | Minimum 7+ years in complex sales or account management, excellent communication skills, and ability to work in a regulated environment. | At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters. The Position Key Account Manager - Roche Sequencing The Opportunity: As a Key Account Manager for Roche Sequencing, you will be responsible for maintaining and growing strategic accounts by fostering exceptional relationships with key stakeholders and aligning customer needs with Roche Sequencing's comprehensive portfolio of solutions. In this role, you will leverage your expertise to achieve sales targets, drive long-term partnerships, and deliver value-added solutions that support customers’ research and clinical objectives. Key Responsibilities: Account Management & Customer Relationships: • Serve as the primary point of contact for strategic accounts, managing and nurturing long-term relationships. • Meet regularly with customers to assess evolving needs and ensure satisfaction with Roche Sequencing’s products and support. • Proactively assess, clarify, and validate customer needs on an ongoing basis to deliver tailored solutions. ​ Strategic Planning & Execution: • Lead joint account planning processes with key customers, establishing mutual performance objectives, financial targets, and critical milestones for both one- and three-year timeframes. • Develop and execute strategies to achieve assigned sales quotas and revenue targets within designated strategic accounts. • Coordinate cross-functional resources — including support, service, and management specialists — to meet account performance goals and exceed customer expectations. Customer-Centric Solutions: • Apply a customer-focused selling approach to drive results, build partnerships, and ensure long-term satisfaction. • Stay informed about key market trends and competitive dynamics to identify and capitalize on new opportunities. • Act as a trusted advisor to customers, effectively communicating the value of Roche Sequencing’s portfolio and assisting them in achieving their research and clinical outcomes. Communication & Collaboration: • Clearly communicate progress on initiatives to internal teams and external stakeholders through regular updates and presentations. • Collaborate closely with internal teams (e.g., Customer Service, Technical Support, Marketing) to address customer concerns, resolve issues, and ensure high levels of satisfaction. • Coordinate with company executives and Customer Service Representatives to address challenges, maintain responsive communication, and resolve problems efficiently. Sales Leadership & Business Growth: • Proactively identify opportunities to expand Roche’s footprint within strategic accounts. • Demonstrate in-depth knowledge of Roche Sequencing’s portfolio to provide comprehensive support across sequencing platforms, software, and informatics capabilities. • Represent Roche at customer engagements, conferences, and key industry events to promote the brand and strengthen relationships. This is a National field-based role. Candidate can be based anywhere in the U.S. Relocation assistance is not provided for this role. Majority of accounts based in CA, AZ and East Coast. Travel Requirements: • Estimated travel, greater than 50%. Who You Are: You bring a passion for managing relationships and driving value for strategic customers. You thrive in roles where you serve as a trusted partner, offering deeply personalized solutions that meet complex customer needs while achieving company objectives. Minimum Qualifications: • You hold a Bachelor’s degree or equivalent experience. • You hold a minimum of 7+ years of proven success in complex sales or account management roles. • Excellent oral and written communication skills, with the ability to deliver impactful presentations. • Strong organizational and strategic planning skills to manage multiple accounts and initiatives simultaneously. • Proven leadership abilities • Ability to work in a regulated environment Preferred Qualifications: • Capital sales experience, particularly in sequencing, diagnostics, or life sciences. • Deep knowledge of next-generation sequencing (NGS) technologies, platforms, methodologies, and applications. • Previous experience working with large reference labs, clinical sequencing provider labs and other strategic key opinion leaders. • Familiarity with working across multiple customer call points (e.g., core lab managers, directors, clinicians, purchasing, research and development leads, C-suite executives). • Hands-on experience with CRM tools and strong proficiency with Google Suite of products • Exceptional negotiation skills paired with a solutions-oriented, problem-solving mindset. Key Attributes for Success: • Customer-focused with a strong ability to assess and address client needs effectively and efficiently. • Self-motivated and results-driven with a track record of achieving sales quotas and building long-term partnerships. • Ability to navigate complex organizational structures, coordinate cross-functional teams, and drive alignment toward shared objectives. The expected salary range for this position based on the primary location of CA is $129,200 - $240,000. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. This position is eligible to earn incentive compensation that is calculated and paid in accordance with the applicable Incentive Compensation Plan for the role. This position also qualifies for the benefits detailed at the link provided below. Benefits #LI-JW2 Who we are A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact. Let’s build a healthier future, together. Roche is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws. If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants.

Lead electrical engineering design and delivery for complex laboratory and vivarium facilities ensuring safety, quality, and schedule adherence. | Bachelor's in Electrical Engineering, 15+ years experience in electrical design for pharmaceutical/biotech labs, PE license desirable, expert knowledge of electrical codes and lab standards. | Genentech is establishing a new Campus Development Team (CDT) to oversee the implementation of the Campus Vision Plan (CVP) for the South San Francisco campus. This Principal Electrical Engineer position provides single-point accountability for the successful end-to-end delivery of all electrical and low voltage systems, with a primary focus on the complex laboratory and research environments within the gRED development. This role will also provide expertise for the supporting Vivarium, Utility Plant, and Electrical Distribution Hub as part of the CVP. The Principal Electrical Engineer works within a large, cross-functional project organization and serves as the primary technical liaison, coordinating the specific power, reliability, and low-voltage needs of scientific and vivarium user groups into actionable engineering designs. This position is responsible for ensuring all electrical and low voltage systems are delivered safely, on schedule, within budget, and to the highest standards of quality, meeting the critical demands of a world-class R&D and animal care facility. The Opportunity Responsibilities The responsibilities for this position may include, but are not limited to: Provides technical leadership and deep subject matter expertise for the electrical engineering designs supporting gRED research laboratories, specialized vivarium spaces, and associated supporting projects. Actively leads the design and planning of electrical systems critical to laboratory operations and specialized vivarium environments. Coordinates with the Utility Master Plans to ensure that upgrades to critical electrical infrastructure (including the Regional Utility Plant and Electrical Distribution Hub) directly support the reliability, redundancy, and scalability required by the new lab facilities. Serves as a respected industry expert on laboratory electrical design, engaging with the Roche/Genentech internal and industry external network to learn, influence, and collaborate on new technologies and best practices for gRED. Primary focus will be ensuring scientific user requirements are incorporated into robust technical solutions for the gRED project. Provide expert design guidance on medium/low voltage power distribution to labs and strategies for flexible “plug-and-play” power and robust emergency power/UPS systems to protect critical experiments, data, and animal life-support systems. Work closely with other technical leads to ensure seamless integration of fire alarm, security, and voice/data systems with lab-specific platforms like Building Automation Systems (BAS) and environmental monitoring systems. Serve as the electrical SME in all design and user-group meetings, providing clear technical options analysis and advocating for designs that prioritize scientific workflow, flexibility, and safety. Ensure all electrical designs align with Roche/Genentech and site-specific standards, with a particular focus on standards governing laboratory design and vivarium operations. Coordinate the electrical scope into a comprehensive strategy to address the technical needs across all aspects of the gRED project, from main infrastructure to the point-of-use in the lab. Support broad Design Engineering & Construction Services process improvement projects and LEAN initiatives, applying these principles to improve the lab design and delivery process. Drive innovation in electrical systems specifically for R&D environments, adopting technologies that improve lab flexibility, energy efficiency, and operational reliability. Participate in the development of a project-wide electrical infrastructure strategy to ensure the new gRED labs are adaptable for future scientific platforms and technologies, reducing total cost of ownership while maximizing uptime and research continuity. Key Tasks Project Planning and Coordination: Develop and maintain a comprehensive project plan, coordinating with architects, engineers, and contractors. Apply innovative thinking to proactively identify and mitigate risks while monitoring progress via KPIs and reporting status to management. Budgeting and Resource Management: Support the development and management of the project budget, ensuring cost control and effective resource allocation. Assist with procurement activities, including vendor selection, contract negotiation, and material acquisitions. Stakeholder Management: Build and maintain strong relationships with internal and external stakeholders, fostering collaboration, transparency, and alignment. Serve as a trusted liaison, keeping all parties informed and engaged through regular meetings and progress reports. Team Leadership: Provide effective leadership by clarifying roles and fostering a collaborative, motivated work environment. Mentor and guide team members while contributing strategic design and technical expertise to the facility’s construction. Quality Control and Safety: Implement and enforce strict quality control measures to ensure compliance with industry standards and specifications. Conduct regular inspections and audits to proactively identify and promptly address any quality or safety concerns. Who You Are Requirements Education: Bachelor’s degree in Electrical Engineering or equivalent. Electrical Professional Engineering (PE) in the State of California is desirable. Experience: 15 years or more of hands-on experience in the design, construction, and commissioning of electrical systems for complex pharmaceutical, biotech, or vivarium facilities. Demonstrated portfolio of successfully completed R&D laboratory projects, showcasing expertise in powering and grounding sensitive scientific equipment (e.g., mass specs, NMRs, electron microscopes) and managing high-density equipment loads. Deep expertise in designing critical power infrastructure for research environments, including emergency generators, UPS, and redundant distribution strategies to protect high-value assets, long-running experiments, and animal welfare. Knowledge: Expert-level knowledge of NEC, NFPA, IEEE, OSHA standards, and standards specific to labs and animal facilities. Experience with energy-efficient lab design is highly desirable. Lab and vivarium project design experience is highly desired but not required. Skills: Excellent communication (written/verbal), presentation, leadership, interpersonal, collaborative, conflict resolution, and negotiating skills (especially in translating complex engineering concepts to scientific stakeholders). Exceptional organization and planning skills. Advanced Microsoft Office and Google Suite skills. Teamwork and collaboration skills to facilitate cross-functional and interdepartmental efforts. Attributes: Must be dependable, attentive to details, and proficient in coordination tasks. Self-starter with the ability to work with minimum or no supervision. Relocation benefits are not available for this posting. The expected salary range for this position based on the primary location of California is $168,100 - $312,300 USD Annual. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance. This position also qualifies for the benefits detailed at the link provided below. Benefits Genentech is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws. If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants. Who We Are Genentech, a member of the Roche group and founder of the biotechnology industry, is dedicated to pursuing groundbreaking science to discover and develop medicines for people with serious and life-threatening diseases. To solve the world's most complex health challenges, we ask bigger questions that challenge our industry and the boundaries of science to transform society. Our transformational discoveries include the first targeted antibody for cancer and the first medicine for primary progressive multiple sclerosis. The next step is yours. To apply today, click on the "Apply for this job" button. Genentech is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws. If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants.

Design, optimize, and troubleshoot high-throughput sequencing assays and workflows for clinical diagnostic applications, develop and maintain bioinformatics tools and pipelines, and collaborate with multidisciplinary teams. | PhD or Master's in Bioinformatics or related field, 4+ years industry experience in clinical diagnostics, proficiency in R/Python, strong molecular biology knowledge, and experience with sequencing data and workflow management. | At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters. The Position We are seeking a talented and highly motivated Bioinformatics Scientist to support the development of Roche Diagnostics Molecular Assays that have a global impact on patient care. This role requires a broad understanding of assay development across diverse technologies, including NGS, Nanopore sequencing, and PCR. The successful candidate will collaborate closely with bioinformaticians, wet lab scientists, and external customers to design, implement, and maintain internal algorithms and tools for clinical diagnostic assay development. The Opportunity: • Collaborate with multidisciplinary teams of molecular and computational biologists, as well as wet lab scientists, to design, optimize, and troubleshoot advanced high-throughput sequencing assays and workflows for clinical diagnostic applications. • Contribute bioinformatics expertise throughout the assay development lifecycle, including initial sequencing, validation, and production implementation, by developing and maintaining analytical tools and pipelines for processing diagnostic data from tumor, germline, and cell-free DNA samples. • Create, implement, and streamline bioinformatics tools and workflows in partnership with wet lab scientists to enhance assay development efficiency and data quality. • Provide hands-on troubleshooting to ensure data quality, integrity, and accessibility across the diagnostic workflow, while addressing the needs of internal and external stakeholders through scientific and business analyses. • Advocate for best practices in documenting, training, and scaling algorithms, tools, and workflows to ensure reproducibility and scalability. • Clearly communicate project outcomes and team progress across various teams and organizational functions to promote alignment and collaboration. Who You Are: • You have a PhD or Master's degree in Bioinformatics, Computational Biology, Statistics, or a related field. • You have 4+ years of industry experience in clinical diagnostics or a related domain. • You have expertise in DNA/RNA sequencing data analysis and interpretation. • You are proficient in programming skills in R and/or Python, with experience working in a distributed Linux environment. • You are proficient in creating clear, insightful visualizations of complex biological data, with strong presentation skills to effectively communicate results to both technical and non-technical audiences. • You have a strong understanding of molecular biology principles and hands-on familiarity with next-generation sequencing laboratory processes. Able to work closely with bench scientists to troubleshoot experimental and workflow issues. • You are skilled in writing and maintaining bioinformatics workflows using workflow management systems such as Snakemake or Nextflow • You have demonstrated the ability to independently develop informatics solutions and contribute to scientific informatics initiatives. • You have a solid understanding of cancer biology and in vitro diagnostics (IVD). Preferred Qualifications: • Proficiency in C++ or Java is a plus. This is a remote position based within the US. The expected salary range for this position is based on the primary location of Pleasanton, CA. 116,750 - $217,000. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance. This position also qualifies for the benefits detailed at the link provided below. Benefits Who we are A healthier future drives us to innovate. Together, more than 100'000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact. Let's build a healthier future, together. Roche is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws. If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants.