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
Drive all internal and outsourced manufacturing activities in EMEA, including vial labeling, secondary packaging, product labeling, rework, and the management of intermediate and finished product flows. Ensure GMP compliance, product quality, and process efficiency, while guaranteeing accurate execution of manufacturing orders in the ERP/QMS system and optimal organization of operations to meet market/customer demand in accordance with established procedures and work instructions
Key Accountabilities
Organization and Planning of Manufacturing Activities
Define and coordinate the schedule for internal and outsourced manufacturing.
Ensure the creation, validation, and monitoring of manufacturing orders in the ERP system.
Optimize resource and capacity utilization to meet deadlines and priorities.
Participate in the S&OP review (forecasts/supply) with all operational departments and Sales/Customer Service.
Management of Internal Operations
Supervise labeling, secondary packaging, and rework activities (disassembly of radiopharmaceutical kits, vial de-labeling).
Ensure compliance with GMP standards in controlled areas, including cleaning, pest control, equipment qualification, and environmental monitoring.
Control traceability and documentation of manufacturing operations, including verification of MBRs and coordination of review and release steps (paper and electronic records).
Coordination of Outsourced Operations
Manage relationships with CDMOs for the manufacturing of radioactive injectable doses and secondary packaging operations.
Monitor contracts, timelines, and compliance of external partners.
Assess subcontractor performance and participate as SME in quality audits conducted at CDMOs.
Management of Product Flows
Oversee the manufacturing and handling of intermediate products (APIs, vacuum vials, buffers, excipients, bioconjugates, antibodies, etc.) and finished products.
Ensure compliance of products intended for engineering, clinical trials, magistral preparations, and commercial markets.
Quality and Compliance
Ensure compliance to local and international regulations (GMP, radiopharmaceuticals).
Collaborate with Quality, Quality Control, QP, and Supply Chain departments for batch release (including Regulatory when applicable).
Drive the development and maintain manufacturing quality documents (PMF, SOPs, Work Instructions, Artwork, etc.).
Trainer for personnel accessing GMP areas.
Leadership and Continuous Improvement
Manage, coach, and develop the production team.
Implement product and process improvement initiatives (Lean).
Define and monitor the manufacturing strategy and departmental risk management.
Education And Experience
Engineering or Graduate degree with a focus on Pharmaceutical Sciences, Chemistry, or a related field.
7+ years in a GMP environment, ideally in pharmaceutical or radiopharmaceutical manufacturing.
Strong knowledge of GMP operations and regulatory requirements.
Experience in managing manufacturing orders in ERP systems (SAP B1 or equivalent).
Coordination of subcontractors and project management.
Leadership, communication, and results-oriented mindset.
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 RECRUITMENT PRIVACY POLICY HERE