Lead the clean-in-place / clean-out-of-place area of a multi-year greenfield pharmaceutical program in Carolina, Puerto Rico. As the subject matter expert, you will set the technical direction, guide the team and drive CQV from startup through qualification.
What you'll do- Lead CIP/COP commissioning, qualification and verification as area owner.
- Give technical direction on cleaning processes, system design and cycle development.
- Coordinate execution with engineering, automation, quality and construction.
- Support other CQV areas as needed (process equipment, utilities, startup, automation).
Requirements- 13+ years of pharmaceutical CQV experience.
- Subject matter expert in CIP/COP: equipment, cleaning processes, system design and C&Q/verification.
- Proven ability to lead a CQV area independently.
- Bachelor's degree in Engineering or a Life Science.
Benefits- Contract: 60 months (multi-year program), with possible extension
- Shift: Administrative, Monday-Friday, on-site 5 days/week
- Start: January 4, 2027
