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
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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