Qa Associate

• Own core elements of the GMP QMS-write, update and review SOPs/records
• ensure Good Documentation Practice
• track SOP review cycles and training
• and maintain complete, compliant records
• Manage quality events-identify and raise deviations, lead root cause analysis, define and implement CAPAs, oversee change control and complete post‑implementation reviews, track metrics and report into the business
• Drive inspection readiness-plan and run self‑inspections, conduct independent audits and risk assessments, and keep current with relevant regulatory requirements
• Supplier & customer oversight-support approvals and liaise with external supplier QA where needed
• Controlled drugs compliance-assist with Home Office licensing requirements as needed
• Broader quality support-help maintain the GACP QMS alongside GMP activities

• A relevant scientific or technical degree (or equivalent experience)
• Experience in a quality focused position within a GMP production environment
• Experience of GMP QMS
• Comfortable working in a dynamic, change‑driven setting
• Knowledge of GACP would be advantageous but training and support will be provided
• to be considered for this position you will need to pass an enhanced DBS Check

Knowledge of GACP