Sentec, a Swiss-American medical technology company established in 1999, specializes in respiratory medicine. The company leverages Deep-Tech to develop and manufacture cutting-edge technologies for complex patients with respiratory conditions. They provide medical professionals worldwide with non-invasive, precise monitoring and effective therapeutic solutions.
The Production/Process Engineer role is a crucial position within the company, focusing on the implementation and optimization of medical device production processes. The successful candidate will be responsible for introducing new medical devices into production, developing new production processes, and ensuring compliance with medical device regulations.
Key responsibilities include developing operating resources, managing industrialization and automation projects, conducting process validation, and maintaining comprehensive documentation. The role requires close collaboration with various departments including R&D, Sourcing, QA, and Production, ensuring adherence to FDA, MDR, and ISO 13485 standards.
The ideal candidate should possess a Bachelor's degree or higher in Mechatronics, Electrical Engineering, or a related field, with at least three years of relevant experience. Experience in microtechnology would be particularly valuable. The position offers the opportunity to work on life-saving products in a dynamic environment with flat hierarchies and interdisciplinary teams.
Working at Sentec means contributing to meaningful projects that directly impact patient care and safety. The company culture promotes active participation in decision-making processes and welcomes innovative ideas from team members. This role represents an excellent opportunity for a skilled engineer looking to make a significant impact in the medical technology sector while working with cutting-edge technologies and processes.