Equipment Requalification Consultants with GMP, CQV & CAPA
Listed on 2026-08-15
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Pharmaceutical
Validation Engineer, Pharmaceutical Manufacturing, Pharma Engineer
Equipment Requalification Consultants with GMP, CQV & CAPA
Role name:
Equipment Requalification Consultants
Work Location:
Swiftwater USA
Start date:
Immediate availability. Job Type: Contract (C2C/W2) Interview:
Phone/Video
Role and responsibilities:
We are seeking consultants experienced in equipment qualification and GMP validation activities to support remediation and requalification programs.
Key responsibilities:
Lead and execute equipment requalification activities. Prepare and review qualification protocols and reports. Perform IQ/OQ/PQ activities. Support CQV execution across production and utility systems. Manage deviations and CAPA linked to qualification activities. Ensure GMP compliance throughout the equipment lifecycle. Collaborate with Engineering, Manufacturing and Quality teams.
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