CQV Lead: Biopharma Validation & Commissioning Expert
Listed on 2026-11-01
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Engineering
Validation Engineer, Regulatory Compliance Specialist, Pharma Engineer, Quality Engineering
Trinity Consultants
- Advent Engineering seeks a CQV Lead to drive commissioning, qualification, and validation of biopharma equipment and systems in cGMP environments. You will author and execute comprehensive CQV plans, collaborate across QA, Engineering, and Operations, and ensure timely delivery of compliant documentation.
The role requires extensive hands-on CQV experience, familiarity with DeltaV/PLC/SCADA, and strong regulatory knowledge to support inspections and continuous improvement
Join us at Trinity Consultants
- Advent Engineering as our next CQV Lead:
Biopharma Validation & Commissioning Expert in IN, United States.
Full responsibilities and requirements are described in the listing above.
Learn more about the CQV Lead:
Biopharma Validation & Commissioning Expert role in the description above.
We appreciate your interest in this position.
Join Trinity Consultants
- Advent Engineering and contribute to our ongoing work.
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