This position leads cross-functional teams to deliver Medical Device Regulation (MDR) project outcomes across the portfolio of tube sets, pumps, devices, and insufflators
Job Summary
This position leads cross-functional teams to deliver Medical Device Regulation (MDR) project outcomes across the portfolio of tube sets, pumps, devices, and insufflators.
The role involves driving planning, execution, and timely completion of technical documentation while proactively managing risks and coordinating internal and external contributors.
Novanta offers a culture that embraces teamwork, collaboration, and empowerment within an expanding global company focused on transforming healthcare through innovation.
Matching Summary
This position leads cross-functional teams to deliver Medical Device Regulation (MDR) project outcomes across the portfolio of tube sets, pumps, devices, and insufflators.
Skills & Requirements
Must-have
5+ years project management experience
Regulated technical environment expertise
Cross-functional team leadership
MDR documentation delivery tracking
Risk assessment and mitigation
Nice-to-have
SAP or Arena PLM knowledge
Lean or NGS-style process improvement
Willingness to travel up to 20%
Strong empathy and emotional intelligence
Experience with minimally invasive medicine
Key Requirements
5+ years PM experience in regulated/technical environment
Strong proficiency in Agile, Waterfall, PMP methodologies