HCLTech is seeking a candidate for Oberdorf, Switzerland, to lead and support New Product Introduction (NPI) activities in a regulated medical device environment. Responsibilities include authoring validation protocols, ensuring compliance with ISO 13485 and MDR, and collaborating with cross-functional teams. Strong experience in medical device regulatory environments, validation activities, and knowledge of PCB development using Altium is required. Proficiency in German or French is preferred. This position offers the opportunity to drive significant process improvements in a dynamic environment.
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