Einführung

Stellenbeschreibung

• Support all quality-relevant packaging processes and collaborate with packaging operations and all relevant interfaces with regard to GMP topics
• Partner with stakeholders and provide GMP support to ensure successful delivery of
• the company goals
• Review of manufacturing specifications and Batch Records (BR)
• Review batch record of finished and semi-finished goods
• Manage actively Deviations, and GMP-Issues
• Actively engage in optimization activities and improvements within IMP Quality CP Switzerland. Coordinate improvement projects and engage in corrective and preventive measures (CAPA)
• Build, verify and implement standard documents (SOPs)
• Actively support the introduction of new packaging processes
• Participate in planning meetings to ensure a timely supply to patients
• A key focus for you will also be to support the ongoing cultural and organizational change towards collaboration, agility and innovation in mindset

Erwartetes Profil

• BSc Degree in Pharmaceutical Engineering/Life Science AND / OR professional experience in the field of quality assurance or production, preferably in the areas of pharmaceutical packaging and / or pharmaceutical industry* 
• Detailed knowledge of relevant GMP guidelines and regulations 
• Technical and process knowledge on topics such as packaging lines, packaging materials and master data management are beneficia
• Proven track record to work towards results, excellent planning and organizing skills as well as analytical capabilities and an innovative manner of solving problems 
• Strong team-player with a high level of self-motivation and being able to inspire others
• Ability to communicate clearly and professionally both verbally and in writing in English as well as in German

Application process