Enter the world of innovative automation solutions in the field of diagnostics, which makes a decisive contribution to improving patient care. Our renowned client, located in the vibrant economic area of Mannheim stands for pioneering technologies and a progressive working environment. Your expertise as a specialist in batch documentation is required to further develop cutting-edge technologies and optimize processes in a dynamic team.
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. Review of batch documents
6. Checking the completed HABs for GMP-compliant documentation including prompt correction in electronic batch review systems
7. Strict adherence to the OLT (Order Lead Time) incl. tracking and requesting the required HAB accompanying documents
8. Collaboration in the processing of measures from GMP requirements
9. Support with GMP audits
10. Support with actions for inspections or QRBs/DRs (e.g. HAB searches in the archive)
11. Revision and creation of documentation-relevant SOPs and implementation of related training courses
12. Electronic recording and evaluation of batch data
13. Participation in process optimization to improve good documentation practice and continuous error reduction
14. Preparation and printing of batch documentation
Your profile
15. Successfully completed scientific studies or completed training as a pharmacist/chemist (m/f/d) or comparable training
16. Sound professional experience in the manufacture of parenterals desirable
17. Good knowledge of GMP regulations and GMP-compliant documentation as well as knowledge of hygiene in the pharmaceutical environment
18. Sound knowledge of IT systems (MES, SAP, Excel, Word)
19. Very good knowledge of German and good knowledge of English