QP / QP Lead – 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 which will include commercial and clinical QP release.

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:

• ~5 years of experience working within QA Pharma with a strong background as a QP
• Sterile experience
• Bachelor's or Masters degree in Pharmacy, Biotechnology, Chemistry or related
• QP Certification recognised under EU Directive
• 2001/20/EC with IMP certification experience pharmaceutical industry, with experience in IMPs being a plus.
• In-depth knowledge of EU GMP, GCP, and applicable regulatory requirements for clinical trials.

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