Quality control for raw materials, intermediates, and bulk
Stability management
Leadership of analytics & pharmacology, microbiology & pharmacology, validation & services, and stability teams
You will be responsible for the entire quality control of starting materials, intermediates, and bulk goods as well as stability management
Job Summary
You will be responsible for the entire quality control of starting materials, intermediates, and bulk goods as well as stability management.
You will lead the areas of Analytics & Pharmacology, Microbiology & Pharmacology, Validation & Services, and the Stability team and significantly shape the strategic further development of the QC organization.
Ferring offers diverse opportunities for individual career planning and personal development in an internationally active and innovative environment, flexible working hours, and 30 days of vacation.
Matching Summary
You will be responsible for the entire quality control of starting materials, intermediates, and bulk goods as well as stability management.
Skills & Requirements
Must-have
Quality Control for raw materials, intermediates, and bulk
Stability Management
Leadership of Analytics & Pharmacology, Microbiology & Pharmacology, Validation & Services, and Stability teams
Workplace safety management system
Budget planning and control
Specification and testing method development
Liaison with national and international authorities
Nice-to-have
Strategic development of QC organization
Experience in aseptic drug manufacturing
International collaboration and intercultural competence
Performance-minded innovator and driver
Key Requirements
Minimum 10 years of experience in pharmaceutical quality control
Extensive leadership experience in managing large, interdisciplinary teams