GSK
VP GMP Clinical Manufacturing Operations
USA - Pennsylvania - King of Prussia +2 · On-site · Director · Full-time · Posted Oct 20, 2026
- Location
- USA - Pennsylvania - King of Prussia
USA - Pennsylvania - Marietta
USA - Pennsylvania - Upper Providence - Experience
- 10+ years in large pharmaceutical or biotechnology.
- Education
- Master’s degree in Chemical Engineering, Process Engineering, Pharmaceutical Sciences, Biotechnology, Chemistry, or a related scientific discipline.
About the job
Leads GSK’s global GMP clinical manufacturing operations, ensuring timely, compliant supply of drug substance and drug product for clinical trials while modernizing operations across six sites.
What you'll do
- Lead a global organization of about 300 employees across six sites and oversee its budget and pilot plant operations.
- Deliver clinical-trial manufacturing and supply, functional strategy, and modernization and digitalization programs.
- Oversee major capital projects, workforce planning, performance management, and organizational change.
What they ask for
- Master’s degree in a related scientific discipline.
- 10+ years of experience in large pharmaceutical or biotechnology, including leadership of GMP manufacturing operations.
- Experience in cross-modality drug development and manufacturing, regulated GMP processes, and global scientific/technical line leadership with significant budget responsibility.
- Experience overseeing multi-year capital projects over £100M and leading organizational change or technology deployment.
Nice to have
- PhD in Engineering or a related scientific discipline.
- Experience leading leaders in a complex matrix organization and influencing senior governance and executive forums.
Tools
GMP, CMC Digital Strategy
Model-written summary · the original posting is authoritative