CordenPharma ist ein führender Anbieter für die Entwicklung und Herstellung von pharmazeutischen Wirkstoffen (APIs), Hilfsstoffen, Fertigarzneimitteln und Verpackungsaktivitäten mit mehr als 2.600 Mitarbeitenden weltweit. Mit unseren Dienstleistungen unterstützen wir Pharma- und Biotech-Unternehmen bei der Herstellung von Medikamenten mit dem vorrangigen Ziel, das Leben der Menschen zu verbessern.

Unser Netzwerk in Europa und den USA bietet flexible und spezialisierte Lösungen auf fünf Technologieplattformen: Peptides, Lipids & Carbohydrates, Injectable, Highly Potent & Oncology; and Small Molecules. Wir sind bestrebt in all diesen Bereichen höchste Qualität zum Wohl der Patienten zu liefern.

Zum nächstmöglichen Zeitpunkt suchen wir am Standort Fribourg eine/n

As Qualification & Process Engineer you will be working as part of the CordenPharma Fribourg Technical Operations Department. You will manage the qualification plan to maintain the accurate qualification state of new and existing equipments for Manufacturing, Packaging & Engineering. 

• Qualification of equipments : you will execute and monitor the qualification status of the new and existing manufacturing, packaging & engineering equipments and systems, manage the whole process of qualification plan (URS/DQ/FAT/SAT/IQ/OQ/PQ) & create qualification, risk analysis, technical &SOPs documentation
• Improvements: You will lead or participate to investigations, improvements and customers requests implementation for equipment and systems under your responsibilities.
• Leadership : You will manage external resources (equipment suppliers) and project teams
• Quality: you will ensure the quality of Qualification activities activities according to GMP guidelines, VMP and internal procedures
• Process: Lead the investigation for deviations linked to equipment and production processes using problem-solving tools and define corrective actions
• Projects: Lead or participate to the implementation of continuous improvement projects for manufacturing and packaging equipment and processes

• Engineering degree, Master of Science, in relevant field (Pharmaceutical industry, Chemistry)
• Min.3 years’ experience with equipment qualification
• Experience with GMP and FDA regulations
• Excellent interpersonal skills, analytical thinking and cost consciousness, great communication skills
• Experience with computer validation (GAMP, 21CFR Part 11, Eudralex Annex 11) & Data Integrity
• Strong oral & written communication skills (English & French; German a plus)