Quality Assurance Associate

Leiden Area | Full-time | On-site/Hybrid Life Sciences | GMP | Documentation | Batch Release Support Are you a recent graduate or early-career professional eager to grow within Quality Assurance in the pharmaceutical industry? We’re supporting a global leader in health and life sciences to build their future talent pipeline in Quality Assurance . Join a company that is passionate about innovation, compliance, and improving patients' lives , and take your first step into a structured, fast-paced GMP environment. Key Responsibilities Support batch documentation review and GMP-compliant archiving Assist in deviation investigations, CAPA tracking, and quality metrics reporting Perform change control coordination and document updates in quality systems Collaborate with cross-functional teams (Production, QC, RA) to ensure timely release processes Help ensure compliance with regulatory requirements (EU-GMP, FDA, ICH guidelines) Ideal Background Bachelor’s or Master’s degree in Life Sciences, Biotechnology, Pharmacy, or Chemistry Internship or up to 2 years of experience in QA/QC/GMP setting (pharma, biotech, medtech) Knowledge of GMP principles and understanding of pharmaceutical manufacturing Strong attention to detail, documentation skills, and eagerness to learn Fluent in English (Dutch is a plus!) What You’ll Get Hands-on training and mentorship from QA professionals Opportunity to work with global QA systems and quality platforms Exposure to cutting-edge pharmaceutical technologies Career development pathways in QA, Validation, Regulatory Affairs, and more

Location: Leiden, South Holland, NL

Posted Date: 8/3/2025