CQV/CSV Specialist – Validation & GMP Compliance Expert
Listed on 2026-09-05
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Quality Assurance - QA/QC
Regulatory Compliance Specialist, QA Specialist - Analyst/Manager
AMTSOL is seeking a CSV/CQV Specialist to support high-priority qualification and validation activities within a cGMP environment. The role focuses on the qualification of analytical instruments, computerized systems and GMP equipment, and on driving inspection-ready validation documentation and backlog remediation.
** Key Responsibilities*
* * Support IQ/OQ/PQ for analytical instruments, computerized systems and GMP equipment.
* Develop and execute validation documentation, including URS, risk assessments, protocols, test scripts, traceability matrices and reports.
* Support CSV, data integrity, 21 CFR Part 11, EU Annex 11 and GMP compliance.
* Partner with QC, QA, Engineering, Automation, Instrumentation and system owners.
* Manage deviations, CAPAs, change controls and validation backlog activities.
* Use Kneat for validation documentation, workflows and approvals.
* Help drive inspection-ready documentation and backlog remediation.
** Requirements*
* * 3--5+ years' experience in CQV/CSV within pharmaceutical, biotech or regulated industries.
* Bachelor's degree in Engineering, Life Sciences, Chemistry, Biology or a related field preferred.
* Strong GMP / CQV / CSV background.
* Analytical laboratory instrument qualification experience.
* Hands-on equipment qualification experience.
* Kneat experience strongly preferred.
* Excellent technical writing and documentation skills.
* Able to manage multiple priorities in a fast-paced environment.
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