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). Do you thrive in a dynamic international environment, leading a cross-functional team to develop innovative digital solutions that significantly impact patients' lives? 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. * Oversee software development lifecycle, including requirements definition, design, verification/validation, and post-market surveillance.
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