Software Project Manager - Medical Device (Bedford, MA)

Software Project Manager – Medical Device (Bedford, MA) We are seeking an experienced and detail‑oriented Project Manager to join a high‑performing team focused on Advanced Imaging products in the Philips Image Guided Therapy Devices (IGT‑D) business. In this role, you will oversee and coordinate software project workstreams supporting the continued commercial expansion of our growing product portfolio. Your work will enable efficient software development practices, regular and predictable release cadences, and continual product improvement. Responsibilities Coordinate cross‑functional design and operations teams to bring software projects through the full product development lifecycle, from definition through commercialization. Act as a key leadership stakeholder to drive development teams to utilize good software development practices, ensuring alignment on project goals, milestones, and accountability of cross‑functional teams. Provide regularly updated project timelines with appropriate levels of detail for determining key risks and dependencies, tracking project deliverables, and clear ownership of deliverables. Identify and assess project risks and opportunities, developing robust mitigation strategies while fostering a culture of thoughtful risk‑taking with escalation to senior management when necessary. Report to the Head of Optical & Systems, Advanced Imaging at Philips IGTD, and work alongside a talented multidisciplinary team of Systems and Software Engineers. Collaborate cross‑functionally with product development, quality, operations, field service, and business stakeholders. Qualifications 6+ years of experience in a project management role focused on software development, with a Bachelor’s Degree in Engineering. PMP certification is a bonus, but not required. Demonstrated experience managing complex schedules and cross‑functional teams. Strong understanding of product development processes and life cycle management, both as a project manager and as an independent contributor. Familiarity with medical device regulations, IEC62304, and regulatory submission processes (e.g., 510(k)). Strong organizational and collaborative skills with a strategic mindset for managing project risk, timelines, and resource allocations. Excellent verbal and written communication skills and an ability to work efficiently with a variety of cross‑functional stakeholders. Must be able to successfully perform the following minimum Physical, Cognitive and Environmental job requirements with or without accommodation for this position. Work Location & Requirements Onsite role; office 5 days a week. Must reside in or within commuting distance to Bedford, MA. Benefits Pay range: $142,000 - $227,000 (actual base pay may vary). Other compensation may include annual incentive bonus, sales commission or long‑term incentives. Eligible for Philips Total Rewards benefits program: generous PTO, 401(k) up to 7% match, HSA with company contribution, stock purchase plan, education reimbursement, and more. Equal Employment Opportunity Philips is an Equal Employment and Opportunity Employer including Disability/Vets and maintains a drug‑free workplace. Legal Notice US work authorization is a precondition of employment. The company will not consider candidates who require sponsorship for a work‑authorized visa, now or in the future. #J-18808-Ljbffr