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QA Auditor CSV
Job Location:
Yearly Salary:
Posted:
19 August 2026 (4 hours ago)
Posted:
Application Deadline:
16 November 2026
Application Deadline:
Vacancies:
1 Vacancy
Vacancies:
Job Summary
QA Auditor / Senior QA Auditor CSV
Hybrid London Permanent
Talentmark is partnering with an innovative UK biotechnology company to recruit a QA Auditor with CSV expertise to join its growing Quality team. Our client is open to candidates at either QA Auditor or Senior QA Auditor level depending on experience.
This is an excellent opportunity for an experienced Quality professional with Computer System Validation (CSV) auditing expertise and a GCP background in a clinical site auditing (esource EQMS and LIMS systems).
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 200 106 in all correspondence.
Hybrid London Permanent
Talentmark is partnering with an innovative UK biotechnology company to recruit a QA Auditor with CSV expertise to join its growing Quality team. Our client is open to candidates at either QA Auditor or Senior QA Auditor level depending on experience.
This is an excellent opportunity for an experienced Quality professional with Computer System Validation (CSV) auditing expertise and a GCP background in a clinical site auditing (esource EQMS and LIMS systems).
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 and 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 (2/3 days on-site).
- Competitive salary and benefits package.
It is essential that applicants hold entitlement to work in the UK. Please quote job reference 200 106 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
