QP
Key Responsibilities:
* Act as a QP for the certification and release of IMPs in compliance with EU GMP regulations.
* Ensure adherence to quality standards, regulatory requirements, and clinical trial protocols.
* Work closely with cross-functional teams, including Regulatory Affairs, Manufacturing, and Quality Assurance.
Requirements:
* QP status eligible under Directive 2001/83/EC.
* Strong IMP experience within a GMP environment.
* Excellent knowledge of EU and UK pharmaceutical regulations.
📍 Location: Greater London Area (4 days on-site, 1 day from home)
💰 Competitive salary + benefits
Interested? Apply now