Job Description
Employment Type: Full-time, 1 year Contract
Industry: Pharmaceuticals / Biotechnology / Medical Devices
About the Role
We are looking for a motivated Validation Engineer / Validation Specialist to support commissioning, qualification, and validation activities within a regulated GxP environment. In this role, you will contribute to ensuring that systems, equipment, and processes meet regulatory, quality, and compliance requirements while supporting complex industrial projects on site.
You will work in dynamic project environments, collaborating with cross-functional teams and applying your technical expertise to a variety of validation challenges across the DACH region.
Key Responsibilities
- Plan, prepare, execute, and document validation activities (DQ, IQ, OQ, PQ)
- Support commissioning and qualification of equipment, processes, utilities, and/or computerized systems
- Prepare and review validation...