EUMDR Project Manager - 27652

EU MDR Project Manager

9-Month+ Contract | 1st Shift | Monday-Friday, 8:00 AM-5:00 PM

Our client, a global medical device manufacturer, is seeking an experienced EU MDR Project Manager to lead a cross-functional team responsible for implementing EU Medical Device Regulation requirements at a manufacturing site.

This role will own project planning and execution, including schedules, risk management, resource coordination, stakeholder communication, and cross-functional deliverables. The ideal candidate has a strong medical device background with direct experience supporting EU MDR or similar regulatory initiatives.

Key Responsibilities

• Lead cross-functional implementation of EU MDR requirements
• Develop and execute the overall project management plan
• Define project scope, milestones, deliverables, and resource requirements
• Develop and manage detailed project schedules and Work Breakdown Structures (WBS)
• Perform critical path analysis and monitor key project workstreams
• Identify project risks and develop mitigation and response plans
• Monitor project progress, timelines, dependencies, and deliverables
• Lead stakeholder meetings and provide regular project status updates
• Coordinate resources and define team roles and responsibilities
• Evaluate project tradeoffs and resolve issues affecting execution
• Partner with manufacturing, quality, regulatory, engineering, and other cross-functional teams
• Escalate risks and issues as needed to maintain project objectives and timelines

Qualifications

• Bachelor's degree in Engineering, Life Sciences, or a related field
• 5+ years of project management experience in the medical device industry
• Experience with EU MDR implementation or similar medical device regulatory requirements
• Strong understanding of regulatory requirements, risk analysis, and mitigation planning
• Experience managing project schedules, WBS, critical paths, and project risk plans
• Demonstrated success leading cross-functional teams and complex projects
• Knowledge of manufacturing processes and quality systems within a regulated environment
• Strong stakeholder management, communication, organization, and problem-solving skills
• Experience with project management and regulatory compliance tools

Advanced education is preferred.

Why Consider This Opportunity?

• 9-month+ contract with a global medical device manufacturer
• Lead a significant EU MDR implementation project
• High-visibility role working across multiple functional teams
• Opportunity to work closely with manufacturing, quality, regulatory, and engineering
• Monday-Friday, first-shift schedule

If you have a strong medical device project management background and experience supporting EU MDR initiatives, apply today!