CSV/CQV Validation Specialist GMP Systems
Listed on 2026-09-30
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Quality Assurance - QA/QC
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Healthcare
Ameri-Partners is seeking a CSV/CQV Specialist to support qualification and validation activities in a cGMP environment, focusing on analytical laboratory instruments, computerized systems, and GMP equipment.
You will deliver inspection-ready validation documentation, manage backlog remediation, and collaborate with QA, QC, Engineering, Automation, Instrumentation, and system owners to ensure compliance with 21 CFR Part 11 and EU Annex 11.
The CSV/CQV Validation Specialist for GMP Systems position in the Bio & Pharmacology & Health, Management & Operations, IT & Technology field is open for applications.
This posting is for the CSV/CQV Validation Specialist for GMP Systems role at Ameri-partners, based in NJ, United States.
We are looking to fill the CSV/CQV Validation Specialist for GMP Systems position at Ameri-partners in NJ, United States.
The CSV/CQV Validation Specialist for GMP Systems role at Ameri-partners is now open for applications in NJ, United States.
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