Senior Manager, Commercial Product Quality

Telix Pharmaceuticals (AMER)

About The Position

The Senior Manager, Commercial Product Quality is responsible for providing strategic and operational quality leadership across Chemistry, Manufacturing, and Controls (CMC) activities to ensure compliance with global Good Manufacturing Practice (GMP) requirements. This role partners cross-functionally with Manufacturing, Quality Control, Operations, Regulatory Affairs, and external manufacturing partners (CMOs/CDMOs) to drive quality excellence, inspection readiness, and robust control strategies throughout the product lifecycle. The position leads the development and execution of quality strategies that support commercial and commercializing programs, ensuring that manufacturing processes, analytical methods, and control systems are designed, qualified, and maintained in a state of compliance. The Senior Manager provides oversight of GMP activities including batch disposition, deviation management, change control, and validation, while proactively identifying and mitigating quality and compliance risks. This role is also accountable for establishing and strengthening quality systems, driving continuous improvement initiatives, and ensuring alignment with regulatory expectations. As a key influencer, the successful candidate builds strong relationships across internal teams and external partners, enabling effective governance and decision-making without direct authority. With a deep understanding of product lifecycles and QA methodologies, the successful candidate will be responsible for overseeing and enhancing quality management systems, driving continuous improvement initiatives, overseeing contract manufacturing organizations, and collaborating with cross-functional teams with a focus on two of our key product projects, Illuccix®, Gozellix®, and TLX090 (153Sm-DOTMP) moving through the commercialization space to commercial product lifecycles. This role is ideal for a proactive leader passionate about quality, committed to delivering exceptional products, and eager to contribute to the continuous growth and success of their organization.

Requirements

Bachelor’s degree in a relevant scientific discipline such as: Pharmaceutical Sciences, Life Sciences (Chemistry, Biochemistry, Microbiology, etc.), Pharmacy, Engineering.
8+ years experience in Quality within the pharmaceutical or biotechnology industry, Manufacturing, Tech Services, and/or Regulatory Affairs.
Strong understanding in GMP, Quality Management Systems, Risk Management, Regulatory frameworks (FDA, EMA, ICH guidelines, etc.).
Excellent leadership and communication skills with the ability to influence and collaborate across departments.
Demonstrated success in driving continuous improvement initiatives and achieving measurable results.
Experience in risk management, root cause analysis, and CAPA (Corrective and Preventive Action) processes.
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.

Nice To Haves

Advanced degree preferred.

Responsibilities

Demonstrate familiarity and compliance with ICH and GMP standards from health authorities worldwide, and guidelines governing the production of Active Pharmaceutical Ingredient (API) Drug Substance, Pharmaceutical Drug Products, Radiopharmaceuticals and medical devices.
Educate business partners on fit-for-purpose GxP requirements, ensuring a comprehensive understanding across teams.
Ensures manufacturing processes meet established quality standards through a formalized system.
Maintain cross-functional relationships with key business partners to guarantee compliance across the scope of manufacturing operations.
Collaborate with matrix teams on pipeline products, addressing Quality needs at the earliest stages of commercialization.
Work closely with contracted manufacturing, testing, or supply chain entities to align their output with Telix commercial needs.
Monitoring performance metrics.
Establishing trending programs.
Performing statistical analysis.
Establishment of acceptance criteria.
Demonstrate in-depth knowledge of regulatory requirements in the life sciences industry.
Communicate and educate cross-functional business partners on regulatory expectations and provide analytical insights.
Provide an assessment of risk when requirements cannot be completely integrated.
Practice meticulous documentation and record-keeping to track activities, decisions, and transactions.
Collaborate with cross-functional business partners and third-party suppliers to ensure all required documentation is captured within Telix, meeting fit-for-purpose criteria.
Develop strategies to enhance cross-functional collaboration.
Mentor and guide QA professions, fostering a collaborative environment to enhance team performance.
Problem-solve cross-functional issues to ensure appropriate relationships with contracted suppliers.
Drive Risk Assessment strategies that mitigate potential issues, ensuring compliance with industry standards and best practices.
Facilitate decision-making, including risk assessment and analysis aligned with health authority requirements.
Take ownership of actions and decisions, earning credibility through consistent delivery.
Grow cross-functional relationships with diverse and efficient thinking, fostering creative approaches.
Navigate through periods of change in company prioritizations, encouraging resilience in others.
Identify areas for process enhancement, utilizing metrics and feedback to drive continuous improvements.