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 pivotal role in the production and packaging of sterile pharmaceuticals. Your daily tasks will involve managing validation and qualification processes, optimizing technical procedures, and applying your expertise within the organization. You will support product transfers, new equipment introductions, and the optimization of existing manufacturing processes. This includes planning and executing technical tests, machine trials, and evaluations. A key part of your role will be creating, managing, and archiving test reports and plans in accordance with regulations, handling deviations, implementing change control measures, and troubleshooting. You will also serve as a technical expert, representing your department in interdisciplinary teams, and effectively sharing insights within the organization. This position offers an opportunity to contribute to innovation, quality, and process optimization in a dynamic team environment.
Required Skills
Education
University degree in Production Technology, Mechanical Engineering, or a comparable scientific 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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