- South East
- £35,000-£50,000 DOE
- Non-Laboratory & Other Scientific Roles
About this job
New opportunity for a driven and highly experienced QA Auditor with a GLP background to join a world-renowned biopharmaceutical testing laboratory.
Working in conjunction with the operational QA team you will assist with all Good Laboratory Practice (GLP) auditing activities. This will include reviewing study plans, final reports, and SOPs, performing audits in relation to bioanalytical and toxicology studies, as well as advising research teams on GLP regulations and ultimately holding responsibility for GLP compliance.
You will need:
- A minimum of 2 years’ experience as a GLP Auditor
- Experience carrying out audits (process, systems & study based)
- An understanding of relevant web-based software (eg TrackWise, Veeva Vault)
- Excellent organisation and communication skills
This position will be home based initially, after lockdown the successful applicant will work onsite at least 3 days a week.
Please note this position is offered as an initial 6-month contract and is highly likely to be extended or made permanent thereafter.
Key words: QA, Quality Assurance, Quality Auditor, Auditor, Audit, Drug Development, Biologics, Drug Substance, SOPs, Change Control, Deviations, Regulatory Guidelines, GLP, Good Laboratory Practice, Technical Documentation, Pharmaceutical, Biopharmaceutical, South East, Berkshire, VRS6680HQ
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