Job Description:

ROLE BRIEF: Quality Assurance Officer - 12 Month FTC

Location: Wales
Salary: £35,000–£45,000 DOE
Contract: 12 months, Fixed Term

Walker Cole International is supporting a well-established pharmaceutical manufacturing organisation in the search for a Quality Assurance Officer to join their Quality team on a 12-month Fixed Term Contract, based in Wales.

This is an excellent opportunity to join a GMP-regulated manufacturing environment, playing a key role in maintaining day-to-day quality compliance and supporting the site's Quality Management System. It offers broad, hands-on exposure across documentation, deviations, CAPAs, change control and audit support, working closely with Production, Quality Control and Regulatory teams.

This role would suit a QA professional looking to build on their GMP experience within a well-established manufacturing site, or someone seeking a structured contract opportunity with the potential for extension.

You will be responsible for:

• Supporting the maintenance and continuous improvement of the site's Quality Management System in line with GMP and regulatory requirements.
• Reviewing and approving batch documentation, ensuring accuracy and compliance prior to release.
• Managing and investigating deviations, non-conformances and CAPAs, including root cause analysis.
• Supporting Change Control processes and maintaining controlled quality documentation, including SOPs and specifications.
• Participating in internal and external audits, including regulatory inspections.
• Supporting supplier and vendor qualification activities.
• Monitoring quality metrics, supporting training compliance, and contributing to continuous improvement initiatives.
• Liaising with cross-functional teams to resolve quality issues in a timely manner.

The successful candidate will have:

• Previous Quality Assurance experience within a GMP-regulated pharmaceutical or biotechnology manufacturing environment.
• A good understanding of Quality Management Systems, GMP and pharmaceutical quality standards.
• Experience managing or supporting deviations, CAPAs, Change Controls and controlled documentation.
• Experience supporting audits or regulatory inspections.
• Excellent communication and organisational skills, with the ability to work across multiple departments.
• A scientific degree or equivalent experience within the pharmaceutical industry.

Quality Assurance | QA | QA Officer | GMP | Good Manufacturing Practice | Quality Management System | QMS | CAPA | Deviations | Change Control | Batch Release | Internal Audit | Regulatory Compliance | Pharmaceutical | Biotechnology | Fixed Term Contract | Wales