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Director, Commercial CMC Programs
Telix Pharmaceuticals LimitedDirector overseeing commercial CMC programs for Telix, a radiopharmaceutical company developing targeted radiation products. Managing manufacturing, CDMO partnerships, supply chain, and clinical-to-commercial execution.
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in CMC strategies, overseeing manufacturing and operational plans for clinical and commercial assets, while managing cross-functional teams and external partnerships. Proficient in cGMP manufacturing, contract manufacturing, and quality management with a focus on continuous improvement and performance metrics.
Highest-signal resume keywords
CMC Strategy ExecutionCross-Functional Team ManagementCGMP Manufacturing ExperienceContract Manufacturing LiaisonSterile Injectable Filling
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Manufacturing OperationsQuality ManagementBudget ManagementCapacity ManagementComplex FormulationsSecondary PackagingLyophilizationPrecision MedicineSupply Chain CoordinationMetrics Scorecard Development
Soft Skills
Strong CommunicationCollaborationAdaptabilityEthical BehaviorContinuous Learning
Industry Keywords
CGMPContract Manufacturing OrganizationsBiologicsDrug ProductParenteral DrugsClinical-to-Commercial ProgressionExternal Contract ManufacturerPerformance ManagementCommercial CMC ProgramsOperational Plans
About the role
Key responsibilities & impact- Develop manufacturing and operational plans for commercial and late-stage clinical assets
- Oversee a team of CMC program leads
- Ensure 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 global production, supply chain, logistics, and distribution supporting clinical-to-commercial progression
- Partner with contract manufacturers and serve as liaison and escalation point for the External Contract Manufacturer network
- Oversee manufacturing, quality, and product development from mid-stage clinical through commercial manufacturing
- Manage contracts, budgets, cost savings, and capacity management
- Sustain ECM strategy with Manufacturing Operations, Biologics, Radiochemistry, CMC Programs, Supply Chain, and Procurement
- Coordinate internal and external communications and resolve business issues
- Lead development and performance management of Commercial CMC Program Leads
- Lead supplier performance business reviews
- Create and populate ECM metrics scorecards and dashboards
- Manage commercial manufacturing budgets and continuous improvement
Requirements
What you’ll need- 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 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
- Strong communication, collaboration, adaptability, ethical behavior, and continuous learning capabilities
Benefits
Comp & perks- Annual performance-based bonuses
- Equity-based incentive program
- Generous vacation
- Paid wellness days
- Support for learning and development
- Competitive salaries