Are you looking for a position where your analytical precision and quality awareness directly contribute to product safety and quality? Our focus is on the highest standards – and that's where you come in. To strengthen our QC team, we are seeking a dedicated expert for the continuous development and optimization of our chromatographic analyses in compliance with strict GMP requirements.
Here's what we offer
1. Attractive salary and long-term job security through affiliation with a large corporation.
2. Up to 30 days of vacation per year
3. Company pension scheme contribution after the end of the probationary period
4. Extensive social benefits, including Christmas and holiday pay
5. Reimbursement of travel expenses
6. Usually an open-ended employment contract
7. Good opportunities for acquisition with our business partners
8. Tailored professional development opportunities and free language courses
9. A wide range of employee benefits
Your tasks
10. Your responsibilities include the independent planning, execution, and evaluation of product project work packages, particularly within the framework of method validations and transfers of chromatographic procedures.
11. They are responsible for independently evaluating and statistically analyzing non-routine activities and creating the corresponding GMP documents, including their technical interpretation.
12. Furthermore, you will carry out all activities in compliance with applicable GMP regulations and actively support the review of GMP-relevant documentation.
13. You apply your sound expertise in the field of analytical chromatography specifically to complex analytical methods, taking into account both internal and external quality control requirements.
14. In addition, you will participate in the planning and coordination of processes and contribute to ensuring smooth cooperation with internal and external interfaces.
Your profile
15. Completed studies in natural sciences (Diploma, Master or Bachelor with initial relevant professional experience) or completed vocational training (e.g. chemical laboratory assistant) with many years of relevant professional experience
16. Experience in the GMP environment, especially in the creation and editing of GMP-relevant documentation
17. Several years of professional experience in quality control, ideally with a focus on chromatographic methods
18. Confident use of MS Office applications
19. Independent, structured and very well-organized work style as well as a high quality awareness
20. Strong teamwork and communication skills in professional exchange
21. Excellent German skills for daily team communication, as well as good written and spoken English skills, especially for understanding and creating documentation.
22. Willingness to be present on-site and to work flexible, team-oriented hours.