Posted 2w ago

Quality Release Specialist

@ Clinigen
Byfleet, England, United Kingdom
OnsiteFull Time
Responsibilities:Managing records, Creating documentation, Investigating issues
Requirements Summary:Degree in Life Sciences, Pharmacy or Chemistry; QA experience; GMP/GDP knowledge; WDA(H), MS and MIA(IMP) licence understanding; strong organizational and IT skills; effective communicator; adaptable and detail‑oriented.
Technical Tools Mentioned:Microsoft Office
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Job Description

Clinigen is a rapidly growing global specialty pharmaceutical and services company with a unique combination of businesses. Our divisions operate in a complex global regulatory environment and ensure that vital medicines are delivered securely on time and wherever they are needed in the world.

We are currently 1,100 people headquartered in the UK with global offices in the US, EU, JAPAC and South Africa. Clinigen has grown rapidly since it began in 2010 and is positioned well for an exciting future of continued expansion.

We are seeking a proactive and detail‑driven Quality Release Specialist to support our Quality and Warehouse teams. This role plays a key part in ensuring compliance with Good Manufacturing Practice (GMP) and Good Distribution Practice (GDP), supporting the effective operation of the Quality Management System (QMS), and safeguarding product quality and patient safety.

You will work closely with cross‑functional teams, external partners and regulators, providing both technical and administrative quality support across a wide range of activities.