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Senior Qa Auditor - Csv
Job in
Bristol, Bristol County, BS1, England, UK
Listed on 2026-11-01
Listing for:
Ck Group
Full Time
position Listed on 2026-11-01
Job specializations:
-
Quality Assurance - QA/QC
QA Specialist - Analyst/Manager, Regulatory Compliance Specialist, Quality Control - QC Analysts/Managers
Job Description & How to Apply Below
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 background in a clinical site auditing (esource, EQMS and LIMS systems).
The Role:You'll play a key role in maintaining and enhancing the organisation's 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 clinical sites and CSV (Computer System Validation).
Position Requirements
10+ Years
work experience
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