Quality Auditor
Posted 1 week ago by CK Group- Science, Clinical and Technical
£26 Per hour
Inside
Hybrid
London
Summary: CK Group is seeking a Quality Auditor for a biopharmaceutical company on a 6-month contract. The role involves reviewing clinical batch records, conducting audits, and ensuring compliance with GMP standards. The position requires a relevant scientific degree or equivalent experience in a QA role within a GMP environment. The role is primarily remote with occasional on-site work in London.
Key Responsibilities:
- Be responsible for the final review of clinical batch records.
- Compilation and approval of data packs and presentation to the QP for final release.
- Conduct routine audits of data, information, procedures, equipment, and systems.
- Review and approve production and analytical documentation accompanying the release of API, Safety Assessment, or clinical supply lots.
- Perform audits or inspections of assigned areas or systems to assess compliance with regulatory and Company standards.
Key Skills:
- Hold a relevant scientific degree or have equivalent working experience.
- Experience in a QA or similar role in a GMP environment.
- Previous experience in the pharmaceutical industry.
- Good knowledge of GMP standards and requirements.
- Experience in audit procedures would be an advantage.
Salary (Rate): £26.00/hour
City: London
Country: UK
Working Arrangements: hybrid
IR35 Status: inside IR35
Seniority Level: Mid-Level
Industry: Other
CK Group are recruiting for a Quality Auditor, to join a biopharmaceutical company, on a contract basis for 6 months.
Salary: From £20.00 - £26.00 per hour PAYE, depending upon experience.
Quality Auditor Role:Be responsible for the final review of clinical batch records.Compilation and approval of data packs and presentation to the QP for final release.Conducts routine audits of data, information, procedures, equipment and systems.Review and approve production and analytical documentation accompanying the release of API, Safety Assessment or clinical supply lots.Perform audits or inspections of assigned areas or systems to assess compliance with regulatory and Company standards.Your Background:Hold a relevant scientific degree or have equivalent working experience.Experience in a QA or similar role in a GMP environment.Previous experience in the pharmaceutical industry.Good knowledge of GMP standards and requirements.Experience in audit procedures would be an advantage but the client may also be interested in candidates with QA background with no audit experience.
Company: Our client is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. They have an interdependent global manufacturing network that's committed to delivering a compliant, reliable supply to customers and patients on time, every time, across the globe.
Location: This role is based at our clients site in London for one or two days per week, with the rest home working.
Apply: It is essential that applicants hold entitlement to work in the UK. Please quote job reference 136 692 in all correspondence. Please note: This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check. If this position isn't suitable but you are looking for a new role, or if you are interested in seeing what opportunities are out there, head over to our LinkedIn page (cka-group) and follow us to see our latest jobs and company news. INDKA