EU MDR Project Manager Location:

Onsite Employment Type:

9-Month+

Contract Schedule:

1st Shift | Monday-Friday | 8:00 AM-5:00 PM Opportunity Overview Our client, a Global Medical Device Manufacturer , is seeking an experienced EU MDR Project Manager to lead a critical regulatory implementation initiative within a manufacturing environment. This role will lead a cross-functional team responsible for implementing EU Medical Device Regulation (EU MDR) requirements while managing project plans, timelines, risks, and stakeholder communication. The ideal candidate will have strong project management experience within the medical device industry and the ability to drive complex initiatives from planning through execution. Key Focus EU MDR Compliance | Medical Device Project Management | Regulatory Programs | Cross-Functional Leadership | Risk Management | Manufacturing Operations What You'll Do Lead cross-functional teams to implement EU MDR requirements within a medical device manufacturing site Develop and execute comprehensive project management plans Manage project scope, timelines, deliverables, and stakeholder expectations Create and maintain detailed project schedules, work breakdown structures (WBS), and critical path analysis Identify project risks, develop mitigation strategies, and monitor risk response plans Coordinate project activities across engineering, quality, regulatory, and manufacturing teams Communicate project status, risks, and progress updates to key stakeholders Evaluate project priorities, tradeoffs, and resource needs to keep initiatives on track Define team roles, responsibilities, and deliverables to support successful project execution Monitor project performance and adjust plans as needed to meet objectives What We're Looking For Bachelor's degree in Engineering, Life Sciences, Project Management, or related field 5+ years of project management experience within the medical device industry Experience managing EU MDR implementation projects or similar regulatory initiatives Strong understanding of regulatory requirements, risk analysis, and mitigation strategies Experience developing project schedules, WBS structures, critical path analysis, and risk management plans Proven ability to lead cross-functional teams and coordinate across multiple departments Strong organizational, communication, and problem-solving skills Experience with project management software and regulatory compliance tools Knowledge of manufacturing processes and quality systems within a regulated environment Experience managing onsite projects and cross-functional initiatives preferred

Pay:

$75.00 - $79.00 per hour Expected hours: 40.0 per week

Benefits:

401(k) Dental insurance Health insurance Life insurance Vision insurance

Work Location:

In person