Hydrogen Group seeks an experienced CQV Engineer to drive commissioning, qualification, and validation across pharmaceutical manufacturing projects in Clayton, NC. You will develop and execute IQ/OQ/PQ protocols, ensure readiness of equipment, and manage validation deliverables across concurrent projects.
The role requires GMP/regulated environment experience, strong technical documentation, and the ability to work on-site in Clayton, NC with occasional after-hours work during major validations.
#J-18808-LjbffrCQV Engineer - Pharma Manufacturing (On-Site, Clayton) in ga at Unknown Company
This position is listed as full time and onsite.