Lead end-to-end project management of software development initiatives, ensuring delivery on time, within scope, and within budget. * Collaborate closely with marketing, engineering, quality, regulatory, clinical, and product development teams to ensure compliance with relevant medical device standards (e.g., ISO 13485, IEC 62304, MDR, FDA 21 CFR Part 820). * Oversee software development lifecycle, including requirements definition, design, verification/validation, and post-market surveillance. * Have proven project management experience in software development in the medical device or healthcare technology industry, or other regulated industry. We offer great opportunities for personal development. Furthermore, we offer a wide range of professional, social and financial employee benefits in addition to exciting job challenges and continuous professional and personal development.
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