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QA Auditor Senior QA Auditor, GCP
Job Location:
Yearly Salary:
Posted:
8 July 2026 (30+ days ago)
Posted:
Application Deadline:
5 October 2026
Application Deadline:
Vacancies:
1 Vacancy
Vacancies:
Job Summary
QA Auditor/ Senior QA Auditor GCP
Hybrid London Permanent
Talentmark is partnering with an innovative UK biotechnology company to recruit a QA Auditor or Senior QA Auditor to join its growing Quality team.
This is an excellent opportunity for an experienced Quality professional with a strong background in GCP/clinical site auditing and/or Computer System Validation (CSV) auditing. The client is open to candidates at both QA Auditor and Senior QA Auditor level depending on experience.
The Role
Youll play a key role in maintaining and enhancing the organisations Quality Management System ensuring compliance with GxP regulations and supporting continuous improvement across the business. You will be also supporting with regulatory training eQMS and QA projects.
Responsibilities:
It is essential that applicants hold entitlement to work in the UK. Please quote job reference 194 581 in all correspondence.
Hybrid London Permanent
Talentmark is partnering with an innovative UK biotechnology company to recruit a QA Auditor or Senior QA Auditor to join its growing Quality team.
This is an excellent opportunity for an experienced Quality professional with a strong background in GCP/clinical site auditing and/or Computer System Validation (CSV) auditing. The client is open to candidates at both QA Auditor and Senior QA Auditor level depending on experience.
The Role
Youll play a key role in maintaining and enhancing the organisations Quality Management System ensuring compliance with GxP regulations and supporting continuous improvement across the business. You will be also supporting with regulatory training eQMS and QA projects.
Responsibilities:
- Planning and conducting internal audits across GCP and/or CSV activities.
- Performing supplier and vendor audits where required.
- Identifying compliance gaps and driving CAPA activities.
- Supporting regulatory inspections and client audits.
- Contributing to QA projects quality systems and regulatory compliance initiatives.
- Promoting quality culture and continuous improvement throughout the organisation.
- Degree in a scientific or related discipline preferred.
- Experience in Quality Assurance within the pharmaceutical biotechnology or life sciences sector.
- Internal auditing experience is essential.
- Strong experience auditing GCP clinical sites (not laboratories) and/or CSV (Computer System Validation).
- Experience supporting regulatory inspections and external audits.
- Good understanding of GxP regulations and quality systems.
- Join a leading UK biotechnology organisation making a real impact.
- Hybrid working (3 days on-site).
- Competitive salary and benefits package.
It is essential that applicants hold entitlement to work in the UK. Please quote job reference 194 581 in all correspondence.
About Company
Idibu
100 employees
Every business is now operating in an environment that’s susceptible to change. idibu has evolved against this changing backdrop. Whether driven by legislation, technology, customer demand or the economy, businesses now need to be agile and fleet of foot to ensure they can attr ... View more
