Are you looking for a responsible interface function at a leading global company in Ingelheim? As a system specialist, you will actively shape the digital laboratory landscape and ensure quality in a state-of-the-art environment. Become part of an innovative team and put your expertise into practice!
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
Your tasks
4. System administration: Qualification of reference materials and continuous master data maintenance in LIMS.
5. Document management: Key user for test specifications including their independent creation and administration.
6. Support & control: First-level support for users and maintenance of GMP-relevant data in SAP and HAL.
7. Validation & Development: Support in the optimization of complex LIMS systems and implementation of validation activities.
8. Reporting: Preparation of English-language reports for regulatory submissions (CTAA/MAA) and coordination of sample receipt.
Your profile
9. Completed studies (chemistry/pharmacy) or scientific training with relevant professional experience.
10. Sound knowledge of the analytical laboratory and GMP environment, ideally in drug synthesis/analysis.
11. Confident handling of IT systems (e.g. SAP, LIMS) and very good knowledge of Excel.
12. Strong team spirit combined with solution-oriented and clear communication.
13. Business fluent in written and spoken English for international document management.