QP

We are seeking an experienced Qualified Person (QP) with IMP experience to join a leading pharmaceutical company in Greater London. This is a fantastic opportunity to play a key role in ensuring the highest standards of compliance and product quality within a dynamic and growing organisation.

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!