We continuously look to the future with a commitment to deliver innovative quality products that have a positive impact on patient care and the work of . Are you an experienced Software Project Manager with a background in the Medical Device industry? In this exciting position, we are seeking an experienced Software Project Manager to lead complex, cross-functional software projects from concept through regulatory approval and market launch. * 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). * Have proven track record working with medical device regulations (EU MDR, FDA), quality systems (ISO 13485), and software lifecycle standards (IEC 62304).
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