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About the role
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
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