CQV Engineer - Pharma Manufacturing; On-Site, Clayton
Listed on 2026-10-09
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Engineering
Pharma Engineer, Validation Engineer, Process Engineer, Quality Engineering
Location: Stonecrest
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.
The CQV Engineer
- Pharma Manufacturing (On-Site, Clayton) role at Hydrogen Group is now open for applications in GA, United States.
Our organisation is growing, and we are hiring a CQV Engineer
- Pharma Manufacturing (On-Site, Clayton) in GA, United States.
This opening is for the CQV Engineer
- Pharma Manufacturing (On-Site, Clayton) role at Hydrogen Group.
We are seeking a motivated CQV Engineer
- Pharma Manufacturing (On-Site, Clayton) to join Hydrogen Group in GA, United States.
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