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