Quality Specialist - London, United Kingdom - PE Global
Description
PE Global is currently recruiting for a Quality Specialist for a leading multi-national Biotech client based in Central London.This is an initial 6 month contract with strong possibility of extension.
This role will expose you to the full range of investigatory medicinal products in the client's development pipeline, from simple small molecules through to complex immunotherapy treatments, and a chance to make a real difference to patients receiving theselifesaving and life changing medicines.
Role:
- Responsible for the final review of clinical batch records to ensure compliance with GMP and conformance with regulatory filings
- The compilation and approval of this data pack and presentation to the QP for final release is the core function of the role
- Will work closely with global functions supporting the clinical supply chain, as well as clinical manufacturing sites internally and externally around the world to help achieve this
Requirements:
- Ideally you should have existing experience in a QA or similar role in a GMP environment, however we would be just as interested in new graduates with the right attitude and a willingness to learn.
- Excellent communication skills, an ability to manage issue resolution, confidence to work with mínimal supervision, and a keen eye for detail
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