We are currently looking for a Compliance Senior Specialist (m/f/d) for a business partner in Biberach .
Are a secure and fair income and good social benefits just as important to you as a responsible position and a long-term perspective at a research-based pharmaceutical company ? Then join us – your satisfaction is our goal!
Apply online now! We value equal opportunities and welcome applications from people with disabilities, whose inclusion is of particular importance to us.
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. They manage and oversee the document management of complex GMP documents such as OOX, CAPA, Effectiveness Check, Deviation and Risk Analysis, and ensure their timely implementation.
11. They guarantee a consistently GMP- and regulatory-compliant quality status in the area of Quality Control.
12. They actively support audits and inspections by preparing, compiling, and editing relevant documents and presentations.
13. They consistently implement all internal, national and international GMP requirements and regularly participate in relevant training courses.
14. They independently coordinate complex, cross-departmental compliance issues and work closely with internal and external stakeholders.
Your profile
15. Completed studies (PhD, Diploma, Master or Bachelor) with professional experience in the fields of biochemistry, biopharmacy, biology, chemistry or pharmacy; alternatively, a master craftsman's qualification in a natural science (e.g., master pharmacist) with sound professional experience in a GMP-relevant work environment.
16. Several years of professional experience in biotechnological production, quality assurance/control or in a GMP and compliance environment
17. Excellent knowledge of all common MS Office applications and the ability to quickly and confidently familiarize oneself with new programs and digital tools.
18. Excellent interpersonal and intercultural skills as well as very good presentation and communication skills in German and English across various hierarchical levels.
19. Personally, you impress with your strong communication skills, pronounced planning and organizational abilities, as well as an independent, responsible work ethic characterized by initiative, a systematic approach and team spirit.