For a renowned pharmaceutical company based in Biberach we are currently looking for a committed personality as QC Expert (m/f/d).
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
5. Reimbursement of travel expenses
6. Generally an open-ended employment contract
7. Good chances of being taken on by our business partners
8. Tailored further training opportunities and free language courses
9. A wide range of employee benefits
Your tasks
10. Responsibility for planning and coordinating complex processes for quality control of various biopharmaceutical products (e.g. material releases, sample management, stability studies).
11. Responsibility for supporting the laboratory manager in the planning, coordination and evaluation of relevant QC activities and, if necessary, the preparation of approval documents in the context of the development of biopharmaceutical products.
12. Coordination of the analysis documentation of various GMP documents in the department, including complex deviation and change processes as well as complex work instructions.
13. Partially independent response to internal / external inquiries, including assessment and compilation of complex test results, which are interpreted and presented independently or summarized in the form of a report for internal use, partners or authorities, also in English.
14. Ensuring compliance with GxP and other rules and regulations.
15. Preparation of GMP documents such as usage decisions, specifications, plans and reports.
Your profile
16. Completed scientific studies (Master of Science) in the field of chemistry, biochemistry, pharmacy or comparable scientific disciplines with several years of professional experience; alternatively, completed professional training in the fields with many years of relevant professional experience in the pharmaceutical environment
17. Sound knowledge of the GMP environment and practical experience with material releases and/or analytical issues
18. Practical experience with quality management systems, for example Trackwise
19. Very good specialist knowledge and detailed knowledge in the areas of Sample Coordination/Management, Stability Studies and Document Mgmt. that goes beyond the standard (expert knowledge).
20. Good verbal and written communication skills in German and English
21. Independent, careful and very well organized, structured work even under pressure to succeed and meet deadlines