Piper Companies seeks a Validation Engineer to support GMP-regulated operations at a Clayton, NC site. You will lead CQV activities for facility systems, equipment, and utilities in a fully onsite role.
The role requires 5+ years CQV experience, knowledge of aseptic processing, FDA guidance, and collaboration with engineering, quality, IT, and manufacturing to meet regulatory timelines and quality objectives. A Bachelor's in engineering or life sciences is required.
#J-18808-LjbffrOnsite CQV Validation Engineer — GMP Manufacturing in clayton at Unknown Company
This position is listed as full time and onsite.