Sr Program Manager, EU MDR
Core
Lead EU MDR compliance initiatives and remediation projects for Sleep & Respiratory Care devices, ensuring regulatory milestones are delivered on time and within budget.
Role type
Senior Program Manager (Regulatory Compliance)
Builds
Regulatory compliance programs and remediation projects for medical devices
Domain
MedTech / Healthcare / Regulatory Affairs
Required skills
Program management, risk management, cross-functional stakeholder management, process design, quality improvement initiatives, resource allocation, issue resolution
Preferred skills
PMP certification, experience with Philips Patient Safety and Quality (PSQ) programs
Technologies
Philips PM standards
Responsibilities
Lead EU MDR-focused programs from planning through execution; Develop and manage program plans including resource allocation and risk mitigation; Partner with cross-functional stakeholders to drive alignment; Track program performance through KPIs and address risks; Apply program management best practices to foster collaboration.
Seniority
Senior, hands-on IC