Telix Pharmaceuticals (AMER)

Lead global supplier quality strategy, governance, and performance management for a pharmaceutical company. | 15+ years in GMP operations within pharma/biotech, with 7+ years leading global teams in supplier quality, and strong knowledge of GxP regulations. | Telix Pharmaceuticals is a dynamic, fast-growing radiopharmaceutical company with offices in Australia (HQ), Belgium, Japan, Switzerland, and the United States. Our mission is to deliver on the promise of precision medicine through targeted radiation. At our core, we exist to create products that seek to improve the quality of life for people living with cancer and rare diseases. You will be supporting the international roll-out of our approved prostate cancer imaging agent and helping us to advance our portfolio of late clinical-stage products that address significant unmet need in oncology and rare diseases. See Yourself at Telix The Sr Director of Supplier Quality leads the global strategy, governance, and performance management of the supplier quality program. This role ensures that all external suppliers, CMOs, and contract laboratories meet regulatory, quality, and business requirements to enable uninterrupted supply of GMP/GDP materials, components, intermediates, and finished products. The Sr Director of Supplier Quality will demonstrate core strengths in supplier evaluation and selection, monitoring and development. This includes a robust process of working with key business partners and intelligently selecting suppliers based on fit for purpose criteria. The criteria will include measurements of competencies in quality assurance and control, risk management, continuous improvement, collaboration, and communication. The Sr Director will guide the design and maturity of audit programs and will provide leadership in managing supplier audits, and inspections, with a strong understanding of regulations from the major health authorities and associations. As a key member of our corporate quality leadership team, this individual will play a crucial role in ensuring the ongoing compliance, quality standards, and inspection readiness of our GxP suppliers as well as our internal sites and external partners. This role is fully remote with about 30% travel required, including some international travel. Key Accountabilities: Global Supplier Quality Strategy & Leadership Shape the global supplier quality strategy to align with corporate and quality objectives. Develop and maintain governance models and performance frameworks for supplier oversight across all regions. Lead and develop a high-performing, geographically dispersed supplier quality team. Define expectations and guidelines for conducting Person in Plant requirements based on data and risk Supplier Qualification & Lifecycle Management Oversee processes for tracking, monitoring, and communicating supplier-related risks to Quality, Compliance, and Global Influence functional organizations to recognize and address systemic quality issues at external sites and with strategic partners to drive improvements, mitigating risk, and support better inspection outcomes Ensure risk-based qualification aligned with ICH Q9, ICH Q10, and applicable GMP requirements. Guide and development of supplier risk scoring and segmentation to prioritize oversight and audits. Supplier Audits & Compliance Oversight Provide strategic oversight of global audit planning, execution, and follow-up for suppliers, CMOs, and contract labs. Ensure audit observations are addressed effectively, with timely CAPA closure and robust effectiveness checks. Maintain audit programs consistent with FDA, EMA, MHRA, TGA, PMDA, Health Canada, and other health authority expectations. Issue Management & Quality Escalation Lead response and escalation processes for supplier deviations, OOS, critical defects, and supply-related disruptions. Serve as key decision-maker and escalation point within cross-functional supplier crisis management. Partner with Procurement, Operations, and Technical teams to resolve supplier quality issues and drive continuous improvement. Continuous Improvement Oversee the ongoing optimization within Master Control Supplier Quality and where applicable Audit Module and the ongoing maintenance of program outputs for Supplier Quality Create a living Quality Transformation plan around Supplier Quality Initiatives with both internal and external actions Drive implementation of digital tools for supplier monitoring (e.g., eQMS modules, audit management, scorecards). Implement industry best practices for advanced quality analytics, predictive risk modeling, and supplier quality modernization. Collaboration and Communication Coordinate with Manufacturing and other key business partners to maintain a lifecycle approach to supplier and strategic partner relationships Lead the management of the master supplier list for the entire company Leads cross functional teams in Quality improvement initiatives Education and Experience: Bachelor’s degree in Life Sciences, Engineering, or a related discipline, an advanced degree is preferred 15+ years of experience in GMP operations, within the pharmaceutical or biotech industry 7+ years of leading global teams in the pharmaceutical or biotechnology industry 10+ years in GMP supplier quality, external manufacturing, material quality, or technical quality leadership. Proven track record leading global teams and scaling global supplier quality programs Strong knowledge of GxP regulations Skilled at leading teams through ambiguity and driving decisive action. Strong collaboration with Procurement, Operations, Technical Services, Regulatory, and Supply Chain. Proven leadership experience in managing cross-functional teams in a quality-related environment as well as managing strategic partner accountabilities from a supplier quality perspective Excellent communication and interpersonal skills Strong analytical and problem-solving abilities Ability and willingness to travel as needed Key Capabilities: Inclusive mindset: Demonstrate an understanding and appreciation for diversity, and actively work to create an inclusive environment where everyone feels valued and respected Creativity and innovation: Possess a willingness to think outside the box and come up with unique and creative solutions to challenges Commitment to excellence: Take pride in your work and consistently strive for excellence in everything you do Results-oriented: Driven to achieve goals and objectives, with a strong focus on delivering measurable results Ethical behavior: Act with integrity and demonstrate a commitment to ethical behavior in all interactions with colleagues and stakeholders Adaptability: Comfortable working in a dynamic environment, able to adjust to changing priorities, and willing to take on new challenges Strong communication skills: Able to communicate effectively with colleagues and stakeholders at all levels, using clear and concise language Collaboration: Work effectively as part of a team, actively sharing knowledge and expertise to achieve common goals Resilience: Demonstrate the ability to bounce back from setbacks and persevere in the face of challenges Continuous learning: Show a commitment to ongoing learning and professional development, continually seeking out opportunities to expand your knowledge and skills At Telix, we believe everyone counts, we strive to be extraordinary, and we pursue our goals with determination and integrity. You will be part of an engaged and supportive group of colleagues who all have a shared purpose: to help people with cancer and rare diseases live longer, better quality lives. Being a Telix employee means being a part of a unique, global, interdisciplinary team working to deliver what's next in precision medicine. We have hybrid and remote employees located all around the world. We offer competitive salaries, annual performance-based bonuses, an equity-based incentive program, generous vacation, paid wellness days and support for learning and development. Telix Pharmaceuticals is an equal opportunity employer. We evaluate qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, and other legally protected characteristics. VIEW OUR PRIVACY POLICY HERE

Manage government pricing calculations and reporting for Medicare, Medicaid, and other programs, ensuring compliance and accuracy. | 7+ years in pharmaceutical or related government program administration, proficiency with data tools like Excel and Access, and knowledge of government payer policies. | Telix Pharmaceuticals is a dynamic, fast-growing radiopharmaceutical company with offices in Australia (HQ), Belgium, Japan, Switzerland, and the United States. Our mission is to deliver on the promise of precision medicine through targeted radiation. At our core, we exist to create products that seek to improve the quality of life for people living with cancer and rare diseases. You will be supporting the international roll-out of our approved prostate cancer imaging agent and helping us to advance our portfolio of late clinical-stage products that address significant unmet need in oncology and rare diseases. See Yourself at Telix The Government Program Manager will be relied upon for price reporting obligations for programs administered by Centers for Medicare and Medicaid Services (CMS) and the associated contractual obligations. As a member of the Market Access Team, the GPM will perform government pricing calculation activities, including transactional data analysis, calculation execution, documentation, and submission of pricing to the various agencies. The GPM will work to ensure the accuracy and quality of calculations through the ongoing development of the vendor systems integration, as well as support the expansion of our systems for future product calculations and reporting requirements. The GPM will also maintain accurate and up-to-date policies and procedures related to Government Pricing and will partner with the VP and Director, Market Access, to provide critical insights to rebate operations, and support expansion of processes as Telix expands into new therapeutic areas. Key Accountabilities: Expanded knowledge and experience in government pricing calculations and reporting including Medicaid, Medicare, and VA/DOD programs. Reports monthly and quarterly pricing obligations to CMS, including source data reconciliation, calculation, documentation, and pricing submission. Collaborates with cross-functional teams and outside vendors to understand and resolve reconciliation and data issues quickly. Provides the dissemination of data and accuracy of calculations to vendor partners. Works with cross-functional business partners on forecast and accrual estimates, modeling, and analysis. Will develop actionable and tactical recommendations that enable Telix to adapt processes and systems from evolving changes in U.S. government payer practices, policies, relevant legislation, regulations, trends and other dynamics. Establishes and maintains policies, procedures, and standards in support internal/external financial reporting processes, and government regulations and stays abreast of CMS Medicaid rules and guidance changes, Medicare and VA/DOD rules and guidance requirements. Completes special projects. Works closely with internal stakeholders to build the infrastructure and tools to support pricing calculations. Performs the reconciliation of third party and internal transactional data including sales, chargebacks, credits, rebates, fees, and other applicable discounts. Collaborates with Rebate Operations, Trade and Distribution, Trade Account Managers, Third Party Logistics providers, and Accounting for timely resolution of any data processing errors, reconciling items and/or adjustments. Coordinates resolution of data scrubs and/or validations. Assesses data adjustments to government pricing data. Maintains detailed support for all required data modifications. Education and Experience: A bachelor’s degree in business, Finance, Accounting or Public Policy, and/or equivalent working experience. 7+ years of experience in pharmaceutical/biotechnology industry or state agency, with experience in Government Pricing, Accounting/Finance, or other related government payer/program administration experience. Experience with effective management of large datasets and data query tools. Must demonstrate a high level of proficiency with Microsoft Access, Excel, PowerPoint and Word. Ability to manage peak calculation cycle workloads and documentation activities. Strong knowledge/understanding of drug contracting, government and commercial customers, and the distribution channels. Demonstrable knowledge of the current policies and guidelines that affect government programs, pricing and payment adjustments Competencies: Comfortable supporting and collaborating in a fast-paced environment through teamwork and open communication. Executes with a level of high personal accountability to meet mandatory reporting timelines and special project timelines. Ability to prioritize and focus on activities that drive value and increase operational effectiveness. Strong verbal and written communication skills, time management, and organization. Applies experience, structured thinking, emerging knowledge, and trends to help solve problems logically. Ethical behavior: Act with integrity and demonstrate a commitment to ethical behavior in all interactions with colleagues and stakeholders. Continuous learning: Show a commitment to ongoing learning and professional development, continually seeking out opportunities to expand your knowledge and skills. Key Capabilities: Inclusive mindset: Demonstrate an understanding and appreciation for diversity, and actively work to create an inclusive environment where everyone feels valued and respected Creativity and innovation: Possess a willingness to think outside the box and come up with unique and creative solutions to challenges Commitment to excellence: Take pride in your work and consistently strive for excellence in everything you do Results-oriented: Driven to achieve goals and objectives, with a strong focus on delivering measurable results Ethical behavior: Act with integrity and demonstrate a commitment to ethical behavior in all interactions with colleagues and stakeholders Adaptability: Comfortable working in a dynamic environment, able to adjust to changing priorities, and willing to take on new challenges Strong communication skills: Able to communicate effectively with colleagues and stakeholders at all levels, using clear and concise language Collaboration: Work effectively as part of a team, actively sharing knowledge and expertise to achieve common goals Resilience: Demonstrate the ability to bounce back from setbacks and persevere in the face of challenges Continuous learning: Show a commitment to ongoing learning and professional development, continually seeking out opportunities to expand your knowledge and skills At Telix, we believe everyone counts, we strive to be extraordinary, and we pursue our goals with determination and integrity. You will be part of an engaged and supportive group of colleagues who all have a shared purpose: to help people with cancer and rare diseases live longer, better quality lives. Being a Telix employee means being a part of a unique, global, interdisciplinary team working to deliver what's next in precision medicine. We have hybrid and remote employees located all around the world. We offer competitive salaries, annual performance-based bonuses, an equity-based incentive program, generous vacation, paid wellness days and support for learning and development. Telix Pharmaceuticals is an equal opportunity employer. We evaluate qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, and other legally protected characteristics. VIEW OUR PRIVACY POLICY HERE

Lead discovery research projects in tumour microenvironment to develop new cancer therapies, collaborate with external partners, and guide research strategy. | Post-graduate degree in a relevant scientific field, at least 10 years of R&D experience in cancer or radiopharmaceuticals, and proven success in managing complex research programs. | Telix Pharmaceuticals is a dynamic, fast-growing radiopharmaceutical company with offices in Australia (HQ), Belgium, Japan, Switzerland, and the United States. Our mission is to deliver on the promise of precision medicine through targeted radiation. At our core, we exist to create products that seek to improve the quality of life for people living with cancer and rare diseases. You will be supporting the international roll-out of our approved prostate cancer imaging agent and helping us to advance our portfolio of late clinical-stage products that address significant unmet need in oncology and rare diseases. See Yourself at Telix The Director or Tumour Microenvironment (TME) Research will independently lead the design, development and management of a portfolio of discovery research projects aimed at enhancing existing pipeline assets or developing new products that address unmet clinical & commercial needs. This role is pivotal in driving innovation that adds value to Telix’s pipeline and supports long-term strategic objectives. Leveraging deep expertise in TME, cancer biology, radiobiology and oncology, the Director will identify and prioritize opportunities to improve treatment options—whether by expanding indications for current products, optimizing their performance or identifying new cancer targets to create novel diagnostic and therapeutic radiolabeled agents. Working closely with VP, Discovery Science, commercial leadership, Key Opinion Leaders, collaborators, and strategic partners, the Director will stay at the forefront of TME advancements, the field of cancer targets to shape a research theme aligned with Telix’s needs. Other key responsibilities include developing a long-term research strategy, conducting due diligence on new opportunities, and evaluating the feasibility of new assets for progression into preclinical and early-stage development. This role aims to contribute to Telix’s future pipeline by delivering impactful research that both supports clinical innovation that is meaningful to patients and provides commercial success for shareholders. Key Accountabilities Developing and managing a TME research plan in line with Telix’s strategic & commercial needs. Creation of commercially-relevant TME research plans to identify synergies between pipeline programs & research outcomes, to evaluate new cancer targets and to seek ways to add value to existing products in the pipeline. Working collaboratively with commercial leads, development program heads and other R&D leadership to identify clinical and commercial opportunities of interest and prioritize research accordingly. Demonstrated active identification and pursuit of academic or commercial collaborations and novel developments to support the research program. Including evaluating in-licensing opportunities. Leading and Managing research projects with a commercial mindset to deliver meaningful research & clinical outcomes and effective delivery. Establishing effective plans and reporting milestones to deliver impactful research producing measurable research outcomes (e.g. data, patents, publications, conference abstracts) that directly support the design of new clinical studies. Building key relationships, network partnerships and collaborations through research partners, in-house and externally sourced resources to support the conduct of research projects. Manage the delivery of projects on time and budget; building cost-effective resourcing plans, including grant applications where appropriate, for implementation and achievement of research goals. Providing scientific thought leadership on developments in the TME field, encouraging strategic partnerships with industry and academia to identify new opportunities. Embody the role of ‘subject matter expert’ regarding Cancer Target biology for radiation delivery via in-depth literature reviews, analysis of existing cancer biomarker datasets or the conduct of bespoke target validation studies as required. Evaluate scientific opportunities to optimize the performance of existing assets by expanding into new indications of interest (target evaluations), dosing improvements or drug combinations as suitable. Identifying validated or novel cancer targets of interest that are suitable for delivery of a diagnostic or therapeutic radiation payload. Based on understanding of TME and radiobiology; make recommendations for the selection of optimal radioisotope payloads for each targeting agent format. Through self-directed research, attendance at conferences or requests from programs, identify & prioritise prospective new opportunities and review and present data packages on targets or agents suitable for exploration in preclinical studies. Supporting internal programs, key collaborations and potential commercial partnerships by providing technical support and advice. Partnering with a range of internal stakeholders from R&D colleagues, preclinical, clinical, project teams and into development streams and strategic alliances and business development to provide scientific and SME input. Contributing to evaluation of opportunities and building new partnerships for development and commercial opportunities. Education and Experience Post-graduate scientific qualifications required (minimum masters’ degree / PhD preferred) Relevant applied research experience in cancer biology, tumour microenvironment, oncology, radiobiology or radiopharmaceutical drug development projects. At least 10 years of relevant R&D experience with at least 2 years in clinical or commercial drug development. With a solid understanding of the pharmaceutical research environment and development and lifecycle management. Proven prior experience managing complex technical research programs and successful 3rd party academic or commercial collaborations. Key Capabilities: Inclusive mindset: Demonstrate an understanding and appreciation for diversity, and actively work to create an inclusive environment where everyone feels valued and respected Creativity and innovation: Possess a willingness to think outside the box and come up with unique and creative solutions to challenges Commitment to excellence: Take pride in your work and consistently strive for excellence in everything you do Results-oriented: Driven to achieve goals and objectives, with a strong focus on delivering measurable results Ethical behavior: Act with integrity and demonstrate a commitment to ethical behavior in all interactions with colleagues and stakeholders Adaptability: Comfortable working in a dynamic environment, able to adjust to changing priorities, and willing to take on new challenges Strong communication skills: Able to communicate effectively with colleagues and stakeholders at all levels, using clear and concise language Collaboration: Work effectively as part of a team, actively sharing knowledge and expertise to achieve common goals Resilience: Demonstrate the ability to bounce back from setbacks and persevere in the face of challenges Continuous learning: Show a commitment to ongoing learning and professional development, continually seeking out opportunities to expand your knowledge and skills At Telix, we believe everyone counts, we strive to be extraordinary, and we pursue our goals with determination and integrity. You will be part of an engaged and supportive group of colleagues who all have a shared purpose: to help people with cancer and rare diseases live longer, better quality lives. Being a Telix employee means being a part of a unique, global, interdisciplinary team working to deliver what's next in precision medicine. We have hybrid and remote employees located all around the world. We offer competitive salaries, annual performance-based bonuses, an equity-based incentive program, generous vacation, paid wellness days and support for learning and development. Telix Pharmaceuticals is an equal opportunity employer. We evaluate qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, and other legally protected characteristics. VIEW OUR PRIVACY POLICY HERE

Lead the operational readiness and commercial execution of radiopharmaceutical distribution, including vendor management, process development, and cross-functional collaboration. | Minimum 5-7 years in radiopharmaceuticals or PET biomarkers, with deep GMP knowledge, experience managing external partners, and understanding of short half-life products. | Telix Pharmaceuticals is a dynamic, fast-growing radiopharmaceutical company with offices in Australia (HQ), Belgium, Japan, Switzerland, and the United States. Our mission is to deliver on the promise of precision medicine through targeted radiation. At our core, we exist to create products that seek to improve the quality of life for people living with cancer and rare diseases. You will be supporting the international roll-out of our approved prostate cancer imaging agent and helping us to advance our portfolio of late clinical-stage products that address significant unmet need in oncology and rare diseases. See Yourself at Telix The Commercial Operations Director-TLX101Px is responsible for leading the operational readiness and commercial execution of Telix’s TLX101Px program. This role bridges strategy and execution by overseeing manufacturing, logistics and distribution initiatives that enable successful product commercialization. It requires a balance of strategic oversight and hands-on operational leadership to deliver compliant, efficient, and scalable processes. The Director will lead the implementation of the commercial distribution strategy for TLX101Px, including contract execution, process development, and the introduction of new tools and systems. They will provide data and analytics in support of finance, sales and marketing functions and serve as the primary interface for vendor, CMO, and distributor management. This includes sourcing, contracting, and performance oversight to ensure reliable, high-quality supply to customers and sufficient capacity to meet commercial and clinical demand. The successful candidate will collaborate cross-functionally with key stakeholders (including Manufacturing, Quality, Clinical, Supply Chain, Logistics, Regulatory, and Commercial) to align operational activities with business objectives. The role demands strong analytical insight, operational rigor, and collaborative leadership to ensure a seamless product launch and sustained commercial success. Key Accountabilities • Operational Readiness & Launch Execution – Lead the implementation of the TLX101Px commercial distribution strategy, including vendor contracting, process development, and coordination of logistics and supply chain activities to support commercial launch. Partner with cross-functional teams on planning and execution of technical transfer activities, including site training and proficiency. Develop and refine processes for managing production challenges, operational failures, and customer support needs. • Vendor & CMO Management – Establish and maintain strong partnerships with contract manufacturers, distributors, and logistics providers. Oversee performance through KPIs, business reviews, and continuous improvement initiatives to ensure reliability and compliance. • Data, Systems & Analytics – Develop and maintain operational reporting tools, dashboards, and analytics that support the commercial team. Ensure data-driven visibility into manufacturing, distribution and delivery performance. • Quality, Compliance & Risk Management – Partner with Quality, Regulatory, Manufacturing, and Supply Chain teams to ensure compliance. Support audits, inspections and CAPA resolution as part of ongoing operational readiness and continuous improvement. • Cross-Functional Collaboration – Work closely with Clinical, Manufacturing, Regulatory, and Commercial teams to align operational processes with strategic business goals and ensure seamless coordination across functions. • Continuous Improvement & Efficiency – Identify opportunities to streamline workflows and processes, enhance vendor performance, increase geographical footprint, enhance redundancy, and optimize cost and supply chain efficiency to enable sustainable growth and scalability. Education and Experience • Education: PharmD, M.S. or B.S. degree in chemistry, biology or related sciences. Advanced degree preferred. • Experience: • Minimum 5-7 years of leadership experience in the development, production, and commercialization of PET biomarkers or radiopharmaceuticals used in commercial operations. Deep understanding of GMP and commercial product development requirements, including 21 CFR 212 and USP compliance. • Strong understanding of processes and considerations unique to short half-life radiopharmaceutical products. • Proven experience managing external partners, CMOs, and distribution vendors, with a demonstrated ability to drive performance through KPIs and continuous improvement. • Travel as required to perform job responsibilities. Key Capabilities: • Inclusive mindset: Demonstrate an understanding and appreciation for diversity, and actively work to create an inclusive environment where everyone feels valued and respected • Creativity and innovation: Possess a willingness to think outside the box and come up with unique and creative solutions to challenges • Commitment to excellence: Take pride in your work and consistently strive for excellence in everything you do • Results-oriented: Driven to achieve goals and objectives, with a strong focus on delivering measurable results • Ethical behavior: Act with integrity and demonstrate a commitment to ethical behavior in all interactions with colleagues and stakeholders • Adaptability: Comfortable working in a dynamic environment, able to adjust to changing priorities, and willing to take on new challenges • Strong communication skills: Able to communicate effectively with colleagues and stakeholders at all levels, using clear and concise language • Collaboration: Work effectively as part of a team, actively sharing knowledge and expertise to achieve common goals • Resilience: Demonstrate the ability to bounce back from setbacks and persevere in the face of challenges • Continuous learning: Show a commitment to ongoing learning and professional development, continually seeking out opportunities to expand your knowledge and skills. At Telix, we believe everyone counts, we strive to be extraordinary, and we pursue our goals with determination and integrity. You will be part of an engaged and supportive group of colleagues who all have a shared purpose: to help people with cancer and rare diseases live longer, better quality lives. Being a Telix employee means being a part of a unique, global, interdisciplinary team working to deliver what's next in precision medicine. We have hybrid and remote employees located all around the world. We offer competitive salaries, annual performance-based bonuses, an equity-based incentive program, generous vacation, paid wellness days and support for learning and development. Telix Pharmaceuticals is an equal opportunity employer. We evaluate qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, and other legally protected characteristics. VIEW OUR PRIVACY POLICY HERE