Equipment Requalification Consultants with GMP CQV CAPA
Listed on 2026-08-17
-
Pharmaceutical
Validation Engineer, Regulatory Compliance Specialist, Pharma Engineer, Pharmaceutical Manufacturing
Equipment Requalification Consultants with GMP, CQV & CAPA
- Contract
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.
All your information will be kept confidential according to EEO guidelines.
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