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.
Key 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.