QC Validation & Systems Lead
Cheshire
£40,000 – £50,000
Pharmaceutical / GMP Laboratory
The Role
We are seeking an experienced QC Validation & Systems Lead to take ownership of QC laboratory equipment lifecycles and computerized systems within a GMP-regulated environment.
This senior, hands-on role blends equipment validation, CSV, data integrity, and team leadership, ensuring QC operations remain compliant, efficient and inspection-ready at all times.
Key Responsibilities
* Own the full lifecycle of QC laboratory equipment, including procurement, qualification, maintenance, change control, and retirement
* Lead equipment validation activities (IQ/OQ/PQ) and manage site calibration programmes, including oversight of external service providers
* Manage QC equipment and validation status using electronic systems (e.g. LIMS), ensuring GMP compliance and inspection readiness
* Lead Computer System Validation (CSV) and administration for QC s...