Senior CQV Program Lead GMP Asset Startups
Listed on 2026-10-07
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Pharmaceutical
Pharmaceutical Manufacturing, Pharma Engineer, Validation Engineer, Regulatory Compliance Specialist
Lilly seeks a Senior Program C&Q Lead to own commissioning and qualification across a global capital program, aligning CQV strategy with platform and network requirements. You will drive field execution, ensure systems are validated and ready for startup, and handover to Site Operations.
Ideal candidates have 15+ years in CQV within GMP environments, with FAT planning experience and strong leadership, vendor coordination, and regulatory knowledge. Travel up to 35% is expected.
For the Senior CQV Program Lead for GMP Asset Startups position at Biopharma Careers, we are reviewing applications now.
This position is for the Senior CQV Program Lead for GMP Asset Startups role at Biopharma Careers.
We are seeking a motivated Senior CQV Program Lead for GMP Asset Startups to join Biopharma Careers in Huntsville, AL, United States.
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