Direct message the job poster from Barrington James
We’re partnering with a leading pharmaceutical company seeking a QA CSV Specialist to support compliance and validation activities across critical GxP systems. This role is ideal for a quality professional with strong experience in Computer System Validation (CSV) and data integrity within GMP environments.
Responsibilities
* Review and approve validation documentation (URS, IQ/OQ/PQ, risk assessments, traceability matrices).
* Ensure GxP and data integrity compliance for all computerized systems across manufacturing and laboratory operations.
* Support change control, deviation, and CAPA processes related to validated systems.
* Collaborate with IT, Quality, and Operations teams to maintain a validated state throughout system lifecycle.
* Provide audit support and ensure readiness for regulatory inspections.
Requirements
* Proven experience in CSV / QA Validation within the pharmaceutical or biotech sector.
* Excellent documentation, communication, and stakeholder management skills.
* Degree in a scientific, engineering, or quality-related discipline.
How to apply
If you are interested in this opportunity, please send your CV and a short cover letter highlighting your relevant experience. Applications will be handled in confidence and reviewed on a rolling basis.
Seniority level
* Entry level
Employment type
* Contract
Job function
* Quality Assurance
Industries
* Staffing and Recruiting
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