Consultant for GMP compliance and quality assurance in Life Sciences. Engage in validation projects and assist in compliance documentation.
Responsibilities
Participation in the development of optimized qualification and validation concepts
Performing qualifications of high‑tech equipment and systems in the pharmaceutical and biopharmaceutical industry
Participation in risk analyses
Support in validation projects (e.g., cleaning, process and method validations)
Preparation of GMP‑compliant documentation, including Standard Operating Procedures (SOPs)
Review of technical documents and drawings, as well as changes and deviations
Requirements
Degree in Process Engineering, Pharmaceutical Engineering, Biotechnology, Chemical Engineering, Life Sciences Engineering, or a comparable engineering or natural sciences degree
Strong technical understanding and the ability to quickly familiarize yourself with different areas of responsibility
Experience in a GMP environment is an advantage
Independent and solution‑oriented working style
Willingness to travel for on‑site qualification activities; valid driving licence (Class B) required
Very good German and good English language skills
Benefits
Exciting and varied projects
A collegial team and an assigned mentor
Flexible location and working‑time model, and permanent employment contracts
Internal and external training and development opportunities
Open company culture with short decision‑making paths
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