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Salary:
From 17.29 per hourto 28.33 per hourPAYE, depending upon experience.
Quality Specialist Role:
- Responsible for the final review of clinical batch records.
- Ensure compliance with GMP and conformance with regulatory filings.
- Conduct 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.
- Previous working experience in a quality function, within either pharmaceutical or chemical industries.
- Excellent knowledge of cGMP regulations.
- Experience of participating in audits.
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.
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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