For our client, a leading global pharmaceutical company in Mannheim, we are looking for a motivated MES Specialist / MBR Designer to join the production team. In this role, you will actively shape the digital future of manufacturing and build the bridge between IT systems and pharmaceutical quality. Become part of an innovative working environment that has a real impact on patient care.
Here's what we offer
1. Attractive salary and long-term job security through group affiliation
2. Up to 30 days vacation per year
3. Contribution to company pension scheme after end of probationary period
4. Extensive social benefits, including Christmas and vacation bonuses
Your tasks
5. Change management: Preparation, planning and prioritization of MBR changes (Master Batch Record) as part of the Electronic Batch Record.
6. Risk management: Carrying out risk assessments and specifying and planning the necessary test requirements.
7. Test coordination: Execution of system tests and responsible coordination of go-live.
8. Interface function: Cross-value stream communication and coordination of change requirements with the departments involved.
9. Process optimization: Continuous support in the evaluation and implementation of system adaptations.
Your profile
10. Completed studies (B.Sc. / M.Sc.) in the pharmaceutical field, bio/medical technology or a comparable field.
11. First professional experience with IT applications in a GxP-regulated environment as well as knowledge of Computerized System Validation (CSV).
12. Sound knowledge of pharmaceutical production processes.
13. Confident in using standard office software; knowledge of PharmaSuite is a clear plus.
14. Business fluent German and good English skills for working in an international corporate environment.