Lead end-to-end project management of software development initiatives, ensuring delivery on time, within scope, and within budget., Plan, manage, and report on project timelines, deliverables, dependencies, and risks., 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., Drive alignment across business units and manage both internal and external stakeholders., Communicate progress, risks, and mitigations clearly to executive stakeholders and cross-functional teams., Ensure documentation and traceability meet regulatory and audit requirements.