Validation Engineer

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Validation and Quality Assurance Consultant – Hamlyn Williams

Are you an validation expert? Have you worked on pharmaceutical projects? Are you looking for a new role?

We are currently seeking an experienced Validation Engineer to support cleanroom and equipment upgrade projects in alignment with EU GMP Annex 1 requirements. This is a hands-on role focused on maintaining and enhancing sterile manufacturing environments through the validation of new equipment and cleanroom modifications.

Skills required for the Validation Engineer include:

• Proven experience working in a GMP-regulated pharmaceutical or biotech environment.
• Strong understanding and practical application of EU GMP Annex 1, especially regarding cleanroom design, control, and monitoring.
• Experience with cleanroom validation, environmental qualification, and equipment validation in aseptic manufacturing areas.
• Familiarity with sterile assembly processes and layout considerations.
• Excellent documentation and communication skills in English; German language skills are a plus.
• Degree in Engineering, Life Sciences, or a related technical field.

This is a fantastic opportunity to join a large pharmaceutical company in Germany. Feel free to share your CV for immediate consideration.

Additional Information

• Seniority level: Mid-Senior level
• Employment type: Contract
• Job function: Pharmaceutical Manufacturing and Biotechnology Research

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