QP

QP – The Randstad, Netherlands

BioTalent is currently supporting a leading global pharmaceutical organisation that is seeking a highly motivated and experienced QP. You will have the opportunity to work globally with a variety of new products across a range of therapeutic areas.

Key Responsibilities :

• IMP Certification : Certifies IMPs for clinical trials, ensuring compliance with EU and international GMP standards.
• Quality Oversight : Oversees manufacturing and testing, manages deviations and audits, and supports the Quality Management System.
• Regulatory & Documentation : Reviews GMP documentation and provides guidance on evolving regulatory requirements.
• Training & Collaboration : Trains staff and collaborates across teams to uphold quality and compliance.

Requirements :

This is an excellent opportunity to get involved in a global leader whilst working at the forefront of science with a strong culture of collaboration.

Please apply / email your resume with a convenient time to Duncan.johnston@biotalent.com to have a confidential discussion about this opportunity.