Quality Assurance Officer
Posted Today by Walker Cole International
£40,000 Per year
Undetermined
Undetermined
London, England, United Kingdom
Summary: The Quality Assurance Officer role at Walker Cole International involves supporting and maintaining the Quality Management System (QMS) in compliance with GMP standards within a pharmaceutical manufacturing environment. The position requires reviewing and authoring controlled documents, managing deviations, CAPAs, and change controls, and contributing to product quality reviews and regulatory inspections. The ideal candidate will possess strong analytical, organizational, and communication skills, along with experience in a GMP-regulated setting. Familiarity with electronic QMS platforms, particularly Q-Pulse, is highly advantageous.
Key Responsibilities:
- Support and maintain the Quality Management System (QMS) in compliance with GMP standards.
- Review and author controlled documents, including SOPs and batch-related records.
- Contribute to Product Quality Reviews, KPI tracking, and preparation for regulatory inspections.
- Manage deviations, CAPAs, and change controls to drive continuous improvement.
Key Skills:
- Experience within a GMP-regulated pharmaceutical manufacturing environment.
- Strong analytical and organisational skills with excellent attention to detail.
- Solid communication skills and ability to work effectively within a collaborative QA team.
- Experience using electronic QMS platforms, e.g. Q-Pulse knowledge is highly advantageous.
Salary (Rate): £40,000.00 yearly
City: London
Country: United Kingdom
Working Arrangements: undetermined
IR35 Status: undetermined
Seniority Level: undetermined
Industry: Other
Walker Cole International is supporting a specialist pharmaceutical manufacturer in the appointment of a Quality Assurance (QA) Officer to join their growing Quality team. Ensure you read the information regarding this opportunity thoroughly before making an application.
As The Quality Assurance Officer, You Will Support and maintain the Quality Management System (QMS) in compliance with GMP standards. Review and author controlled documents, including SOPs and batch-related records. Contribute to Product Quality Reviews, KPI tracking, and preparation for regulatory inspections. Manage deviations, CAPAs, and change controls to drive continuous improvement.
The Successful Candidate Will Have Experience within a GMP-regulated pharmaceutical manufacturing environment. Strong analytical and organisational skills, with excellent attention to detail. Solid communication skills and the ability to work effectively within a collaborative QA team. xlqdzyr Experience using electronic QMS platforms, e.g. Q-Pulse knowledge is highly advantageous.
Quality Assurance | QA Officer | GMP | QMS | CAPA | Change Control | Deviation | Audit | Compliance | Pharmaceutical | Q-Pulse | Documentation | SOPs | Manufacturing | Quality Systems