EU MDR Project Lead — Medical Devices

JBL Resources; Memphis (TN); On-site; USD 120,000 - 160,000; Full time

Job summary

JBL Resources is seeking a seasoned Project Manager for a medical device initiative focused on EU MDR compliance in the Greater Memphis area. You will lead cross-functional teams, manage schedules and risks, and drive project execution in a regulated environment.

The ideal candidate has 5+ years in medical device PM, strong regulatory and risk analysis skills, and experience with WBS, critical path analysis, and stakeholder communications.

Qualifications

• 5+ years of PM experience in the medical device industry with EU MDR focus.
• Strong regulatory, risk analysis and mitigation under EU MDR.
• Experience in developing and managing schedules, WBS, critical path, risk plans.
• Proven cross-functional leadership and stakeholder communication.
• Knowledge of manufacturing processes and quality systems in regulated env.
• On-site project management experience; NO C2C candidates.

Responsibilities

• Lead cross-functional teams to implement EU MDR requirements.
• Develop and execute the project management plan.
• Identify risks and mitigation strategies for project challenges.
• Maintain regular stakeholder updates on project progress.
• Create and manage Work Breakdown Structure and detailed schedules.
• Analyze critical path and major workstreams to prevent delays.
• Establish risk management plans and resource allocation.
• Define roles, responsibilities, and deliverables for team members.

Skills

Project management

Regulatory compliance

Risk analysis

Cross-functional leadership

Stakeholder communication

Problem solving

Education

Bachelor's degree in Engineering, Life Sciences, or related field

Job description

JBL Resources is seeking a seasoned Project Manager for a medical device initiative focused on EU MDR compliance in the Greater Memphis area. You will lead cross-functional teams, manage schedules and risks, and drive project execution in a regulated environment.

The ideal candidate has 5+ years in medical device PM, strong regulatory and risk analysis skills, and experience with WBS, critical path analysis, and stakeholder communications.