Bioengineer Associate

**Bioengineer Associate**

Executes manufacturing activities in the area of Drug Product according to cGMP guidelines, ensuring batch execution, evaluating test results, resolving issues, troubleshoot manufacturing equipment and make recommendations for resolution.

**Responsibilities**
- Provides front line technical and procedural support, working with the manufacturing team.
- Securing each batch is manufactured safely, on time, in compliance with the batch instructions and quality requirements
- Responsible to establish timely and with high quality the required production documentation (preparation, execution and review of batch records) or other relevant GMP documents for the assigned production area.
- Supports process related investigations and assists in decision making on production issues
- Supports process changes and CAPAs related to processes within required timelines
- Performs training activities of relevant areas as operator and supports others and new joiners.
- Operating, setting up and cleaning production equipment and premises for the production of liquid and freeze-dried drug forms (e.g.:compounding, parts washing, autoclaving, filter integrity testing, visual inspection)

**Your profile**:

- 2-4 years of experience GMP environment on the shopfloor (preferably in sterile manufacturing of Drug Product)
- Fluent in either English and German
- Familiarity with GMP requirements, quality procedures and SOP execution
- Prepared to work flexible working hours

Sounds like a great job?