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.