Validation & Investigation Scientist

Contract until end of 2026 | French mandatory Do you enjoy solving complex manufacturing challenges in a GMP-regulated pharmaceutical environment? We are looking for a Scientist Validation & Investigations to support manufacturing operations through validation, qualification, and investigation activities. You will work cross-functionally with Manufacturing, QA, QC, Engineering, and Technical Services to ensure process robustness, product quality, and compliance. Your Responsibilities Lead deviation investigations and root cause analyses Drive CAPAs and risk-based problem solving Support equipment qualification, cleaning validation, and process validation activities Author protocols, reports, and technical GMP documentation Analyze manufacturing data and support continuous improvement initiatives Contribute to audits, inspections, and product lifecycle activities Your Profile BSc or MSc in Engineering, Chemistry, Pharmacy, Life Sciences, or related field 3–5 years of experience in pharmaceutical manufacturing, validation, quality, or process support Experience in Oral Solid Dosage (OSD) manufacturing is highly preferred Good understanding of GMP/cGxP requirements Strong analytical and technical writing skills Fluent English and French (mandatory) What’s on Offer? High-impact role within a modern pharmaceutical manufacturing environment Exposure to cross-functional MS&T activities Opportunity to further develop expertise in validation, investigations, and process science