We are looking for a proactive individual with a scientific background to take responsibility for the smooth coordination of our international contract manufacturers. From reviewing manufacturing documentation to representing packaging activities in global study teams – you will confidently manage complex processes within timelines and budgets. If you are fluent in German and English and have initial experience in the pharmaceutical industry, we look forward to your energy and organizational skills!
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. In your new role, you will be responsible for coordinating the packaging and labeling of clinical trial materials at international contract manufacturers.
11. Furthermore, you will process and coordinate processes in a dynamic environment and work effectively with contract manufacturers and internal interfaces.
12. Your tasks include developing suggestions for improvement to minimize risks and optimize processes.
13. They are responsible for reviewing the manufacturing documentation of contract manufacturers and ensuring compliance with timelines and budget targets.
14. Representation of packaging and labeling activities in global trial teams for study processing
15. Handling of deviations
Your profile
16. Completed Master's degree in natural sciences with initial professional experience in the pharmaceutical industry or another regulated industry.
17. Experience in the pharmaceutical industry is advantageous ; knowledge of packaging, labeling and supply of clinical trial materials in an international environment, as well as project management and supply chain management, is also beneficial.
18. Excellent MS Office skills as well as a strong willingness and ability to quickly familiarize oneself with new systems and processes.
19. Effective communication with external partners and presentation skills
20. High level of personal responsibility combined with a structured and goal-oriented work style
21. Fluent German and English skills, both spoken and written.
22. Willingness to be regularly present on-site and to work closely with the team; working from home is possible after consultation.