CK Group are recruiting for a Quality Specialist to join a biopharmaceutical company at their site based in London on a contract basis for 6 months initially.
Salary:
Up to £24.59 per hour PAYE
Quality Specialist Role:
- Responsible for the final review of clinical batch records to ensure compliance with GMP and conformance with regulatory filings.
- Responsible for the compilation and approval of the data pack and presentation to the QP for final release.
- Work closely with global functions supporting the clinical supply chain, as well as clinical manufacturing sites internally and externally around the world.
- Review and approve production and analytical documentation.
Your Background:
- Ideally have existing experience in a QA or similar role in a GMP environment.
- Educated to BSc level or equivalent.
- Excellent communication skills.
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 Quality Specialist role will be based at our clients European Business Development and Licensing hub in London.
Apply:
It is essential that applicants hold entitlement to work in the UK. Please quote job reference 55215 in all correspondence.
You must have the right to work in the UK. Learn more
- Agency: CK Group
- Reference: 55215
Website: CK Group
- Posted: 7th March 2023
- Expires: 4th April 2023
