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 . * 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). * Have proven project management experience in software development in the medical device or healthcare technology industry, or other regulated industry. * Have proven track record working with medical device regulations (EU MDR, FDA), quality systems (ISO 13485), and software lifecycle standards (IEC 62304). * Have proficiency with project management tools (e.g., Jira, Confluence, MS Project, or similar).
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