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). 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. * 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. * Are open-minded and eager to drive new software initiatives in a company with a strong legacy in physical ...
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