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Director, Commercial CMC Programs

Telix Pharmaceuticals Limited
August 20, 2026
Remote friendly (United States)
United States
Operations
To contribute to the achievement of the Group’s commercial and strategic goals by developing manufacturing and operational plans for commercial and late-stage clinical assets. As Director, CMC Programs, oversee a team of CMC program leads and ensure effective execution of CMC strategies through cross-functional collaboration of internal and external partners. Coordinate and deliver CMC activities for Precision Medicine Diagnostics and Therapeutics programs, including setting up and solidifying global production, supply chain, logistics, and distribution to support late-phase clinical progression into commercial manufacturing.

Key Accountabilities:
- Partner with contract manufacturers; serve as liaison and escalation point between Telix and External Contract Manufacturer (ECM) network
- Oversee manufacturing, quality, and product development from mid-stage clinical through commercial manufacturing
- Manage contracts to meet expectations and budget targets
- Partner with Directors (Manufacturing Operations, Biologics, Radiochemistry, CMC Programs) to sustain ECM strategy
- Determine ECM cost savings and capacity management strategies
- Develop manufacturing and capacity strategies aligned with current/future marketing strategy
- Establish, own, and manage ECM operating mechanisms with Supply Chain and Procurement
- Coordinate communication across internal/external functions; manage issues for resolution
- Lead, develop, and manage Commercial CMC Program Leads; conduct performance business reviews
- Own ECM metrics for scorecards/dashboards
- Manage commercial manufacturing budget and implement continuous improvement

Education and Experience/Qualifications:
- BA/BS in Engineering, Biology, Chemistry, Business, or relevant field
- 10+ years’ combined experience in cGMP Manufacturing, Contract Manufacturing, Business Development, or Quality
- Experience managing cross-functional teams, external partners, and CDMOs
- Preferred: Sterile Injectable Filling and Lyophilization; Secondary Packaging of Parenteral drugs; complex bulk/biologic drug substance formulation manufacturing
- Experience managing cross-functional teams and International Contract Manufacturing Organizations
- Travel ~30% (domestic/international)

Key Capabilities:
- Commitment to excellence; results-oriented; creativity/innovation; strong communication; collaboration; resilience; inclusive mindset; adaptability; ethical behavior; continuous learning