Director overseeing commercial CMC programs for Telix, a radiopharmaceutical company developing targeted radiation products. Managing manufacturing, CDMO partnerships, supply chain, and clinical - to - commercial execution.
About the role
- Director overseeing CMC manufacturing, supply chain, and contract manufacturers at Telix Pharmaceuticals. Supporting precision radiopharmaceutical products for cancer and rare diseases.
Responsibilities
- Develop manufacturing and operational plans for commercial and late-stage clinical assets in collaboration with Regional Operations leadership, Supply Chain, Program leadership, and the Director of Manufacturing Operations
- Oversee a team of CMC program leads
- Ensure effective execution of CMC strategies through cross-functional collaboration with internal and external partners
- Coordinate and deliver CMC activities for Precision Medicine Diagnostics and Therapeutics programs
- Establish and solidify global production, supply chain, logistics, and distribution supporting late-phase clinical progression and commercial manufacturing
- Partner with contract manufacturers and serve as liaison and escalation point between Telix and the External Contract Manufacturer network
- Oversee manufacturing, quality, and product development from mid-stage clinical through ongoing commercial manufacturing
- Manage contracts, budgets, cost savings, capacity management, and continuous improvement
- Sustain ECM strategy and establish, own, and manage ECM operating mechanisms and oversight
- Coordinate communication across internal and external functions and manage issues to resolution
- Lead, develop, coach, and performance-manage Commercial CMC Program Leads
- Lead performance business reviews with suppliers and contracting organizations
- Create and populate ECM metrics scorecards and dashboards
Requirements
- BA or BS degree in Engineering, Biology, Chemistry, Business or other relevant field
- 10+ years combined experience in cGMP Manufacturing, Contract Manufacturing, Business Development, or Quality
- Experience in managing cross-functional teams, external partners, and CDMOs required
- Experience managing cross-functional teams and International Contract Manufacturing Organizations
- Ability to travel approximately 30% - both domestically and internationally
- Direct experience in Sterile Injectable Filling and Lyophilization of Drug Product/Substances supporting both pre-commercial and commercial products preferred
- Direct experience in Secondary Packaging of Parenteral drugs preferred
- Direct experience in complex formulations of bulk drug substances and biologic drug substance manufacturing preferred
- Commitment to excellence
- Results-oriented approach
- Creativity and innovation
- Strong communication skills
- Collaboration skills
- Resilience
- Inclusive mindset
- Adaptability
- Ethical behavior
- Commitment to continuous learning and professional development
Benefits
- Competitive salaries
- Annual performance-based bonuses
- Equity-based incentive program
- Generous vacation
- Paid wellness days
- Support for learning and development
- Hybrid and remote work arrangements
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