Validation Engineer Sterile Pharmaceutical Production | Validierungsingenieur (m/w/d) Sterile Arzneimittelproduktion in Mannheim (1269)
Brüggen Engineering GmbH
Job Summary
As a Validation Engineer, you will play a crucial role in the production and packaging of sterile pharmaceuticals. You will manage validation and qualification processes, optimize technical procedures, and contribute your expertise to the organization. This involves supporting product transfers, implementing new equipment, and optimizing existing manufacturing processes. You will plan and execute technical tests and machine trials, as well as create and archive test reports and plans in accordance with regulations. Additionally, you will handle deviations, implement change-control measures, provide technical consultation, and present findings to interdisciplinary teams. This is an attractive opportunity for professionals seeking to innovate and ensure quality in pharmaceutical production within a dynamic team.
Required Skills
Education
University degree in Production Engineering, Mechanical Engineering, Natural Sciences, or a comparable field
Experience
- Professional experience in validation, product lifecycle management, and pharmaceutical or biotechnological development
- Experience with production processes such as filling techniques, lyophilization, and filtration
Languages
Additional
- Not specified
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