In the Process Engineering department, in collaboration with the Quality Assurance department, products are transferred from research to production and new GMP processes are developed.
Your responsibilities include:
Supervision of quality aspects and coordination of quality issues with the internal QA department and suppliers
Project planning and coordination of qualifications and validations in accordance with current GMP regulations
Conducting experiments in process development to optimize production processes
Join our process engineering department as part of a dynamic team, where collaboration and support drive our success. You’ll contribute your expertise and ideas while benefiting from ample opportunities for professional growth and development.
As prerequisites for this exciting role, you should hold a university degree in a scientific or technical field such as Biochemistry, Chemistry or Engineering. Preferably, you already gained experience in a GMP environment or in the area of qualifications/validations. You are an analytical thinker and maintain a clear overview even in complex situations thanks to your pronounced organizational skills. You show initiative and entrepreneurial spirit and are excited to participate in the dynamics of an innovative start-up company. Good communication skills and fluency in English is essential; knowledge of German or French is a plus.
Interested candidates are kindly requested to submit a complete application (cover letter, CV and reference letters) to Ms. Noëlle Haas, who can also be contacted for additional information by phone (058 521 35 01) or e-mail (hr@innomedica.com).
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