QA Officer
Posted 2 days ago
- Buxton, Derbyshire
- Any
- External
- Expires In 3 months
Job Title: QA Officer Location: Near Buxton (Fully Onsite)
My client is a contract testing laboratory supporting the healthcare and related industries. We are looking for a highly motivated and detail-oriented QA Officer to join a small and friendly team based in Tideswell, UK. This is an exciting opportunity to work in a fast-paced environment, ensuring the quality and compliance of laboratory work in line with ISO 17025 and GMP standards.
Key Responsibilities :
Ensure compliance with company policies and procedures, including Health and Safety, ISO 17025, and GMP.
Review, write, and amend documentation such as SOPs.
Manage controlled documentation and maintain its circulation and availability.
Audit GMP data, including reviewing raw data prior to releasing GMP CoA or CoP.
Coordinate quality issues, investigations, and CAPA.
Assist with OOS, NC, NTF, CMP, RA, and CAPA investigations.
Participate in the change control process to ensure changes maintain GMP compliance.
Track, trend, and gather data for meetings as per procedures.
Conduct staff training on quality matters when required.
My client is a contract testing laboratory supporting the healthcare and related industries. We are looking for a highly motivated and detail-oriented QA Officer to join a small and friendly team based in Tideswell, UK. This is an exciting opportunity to work in a fast-paced environment, ensuring the quality and compliance of laboratory work in line with ISO 17025 and GMP standards.
Key Responsibilities :
Ensure compliance with company policies and procedures, including Health and Safety, ISO 17025, and GMP.
Review, write, and amend documentation such as SOPs.
Manage controlled documentation and maintain its circulation and availability.
Audit GMP data, including reviewing raw data prior to releasing GMP CoA or CoP.
Coordinate quality issues, investigations, and CAPA.
Assist with OOS, NC, NTF, CMP, RA, and CAPA investigations.
Participate in the change control process to ensure changes maintain GMP compliance.
Track, trend, and gather data for meetings as per procedures.
Conduct staff training on quality matters when required.