Senior EU MDR Program Lead - MedTech

Philips; Cambridge (MA); On-site; USD 135,000 - 216,000; Full time

Job summary

Philips is seeking a Sr Program Manager to drive EU MDR compliance initiatives for the Sleep & Respiratory Care team. You will lead cross-functional programs from planning through execution, balancing scope, budget, and regulatory requirements while engaging stakeholders and managing risks.

The role emphasizes collaboration, continuous improvement, and adherence to Philips PM standards. A strong background in MedTech/regulatory programs and excellent cross-functional communication are essential.

Qualifications

• 5+ years of experience in Program Management, Project Development, Business Strategy, or equivalent within a MedTech or healthcare setting.

Responsibilities

• Lead EU MDR-focused programs from planning through execution, ensuring delivery within scope, timeline, budget, and regulatory requirements.
• Develop and manage program plans, including resource allocation, risk mitigation, and issue resolution to achieve key milestones.
• Partner with cross-functional stakeholders to drive alignment, manage interdependencies, and support strategic business objectives.
• Track program performance through KPIs, proactively addressing risks and challenges to maintain progress and maximize outcomes.
• Apply program management best practices and Philips PM standards while fostering collaboration, transparency, and continuous improvement across teams.

Skills

Program management

Project development

Business strategy

Cross-functional collaboration

Education

Bachelor’s or Master’s degree in healthcare or business administration, Project Management or equivalent

Job description

Philips is seeking a Sr Program Manager to drive EU MDR compliance initiatives for the Sleep & Respiratory Care team. You will lead cross-functional programs from planning through execution, balancing scope, budget, and regulatory requirements while engaging stakeholders and managing risks.

The role emphasizes collaboration, continuous improvement, and adherence to Philips PM standards. A strong background in MedTech/regulatory programs and excellent cross-functional communication are essential.