- Supervision of development projects in interdisciplinary teams for finished medicinal products up to market launch and throughout the entire product life cycle.
- Processing of complaints, deviations and change requests
- Creation, review and maintenance of quality documents (e.g. MBR, PQR, risk assessments, stability program)
- Coordination of all quality-relevant topics relating to finished products with the quality units of our manufacturing partners and our customers
- Presentation of quality processes in customer audits, inspections by authorities and internal audits
- Successfully completed scientific or technical studies
- Several years of professional experience in the pharmaceutical industry, particularly in the area of manufacturing finished medicinal products
- Very good knowledge of GxP guidelines and the relevant ICH guidelines
- Strong communication and teamwork skills
- Enjoy taking responsibility and making decisions
- Very good knowledge of German and English
- We are looking for you as a personality and want you to make an authentic contribution - we encourage this in turn by giving you plenty of scope for creativity and independence
- A career in sales combined with interesting and challenging tasks in a dynamic, constantly growing company
- A secure job in an established and renowned family business that offers you the security of over 35 years in business as well as a personal and respectful working atmosphere
- We have flat hierarchies and small teams without matrix structures. This enables us to have clear and direct communication channels that lead to quick decision-making processes
- Flexible working hours and 30 days' vacation
- Comprehensive training opportunities with a fixed annual training budget
- Various benefits such as JobRad, EGYM Wellpass, employee restaurant, regular events and much more.
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