Associate for Sterile Drug Product Process Development | Mitarbeiter für die Prozessentwicklung steriler Arzneiformen (m/w/d)

Job Summary

This role involves critical process development for sterile drug products, supporting a leading pharmaceutical service provider specializing in aseptic filling and packaging of injectables (syringes, etc.). The Associate will be responsible for defining individual procedural steps, executing practical implementation, and managing the design and procurement of product-contact equipment. Key activities include planning and executing experimental series and process simulations in development laboratories, meticulously documenting raw data and results according to relevant guidelines, and supporting the implementation of new technologies and procedures in production, including GMP batches. Candidates must possess a scientific or technical degree (Master/Diploma) or equivalent qualification, coupled with several years of experience in manufacturing and developing parenteral dosage forms, and fluent English skills. This is an opportunity to contribute to life-saving treatments for diseases like Multiple Sclerosis and cancer within a globally operating, family-owned company.