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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 (Apply online only)in all correspondence.
Please note:
This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.
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