Job Title: Sr Manufacturing Project Manager – Medical Device
Location: Warsaw, Indiana (Onsite)
Duration: W2 Contract (May 2026 – May 2028)
Job Summary:
We are looking for a Senior Manufacturing Engineer / Site Lead to drive EU MDR implementation activities for Spine products at a manufacturing site. This role will lead cross-functional execution, ensure regulatory compliance, and manage project timelines in a highly regulated environment.
Key Skills & Experience:
• Strong Project/Program Management in manufacturing environments
• Hands-on experience with EU MDR / regulatory implementation
• Expertise in change control (ECO/MCO/SMECO) and documentation
• Knowledge of manufacturing processes (machining, assembly, metal finishing)
• Experience working with cross-functional teams (Quality, Engineering, Supply Chain, Operations)
• Ability to manage timelines, risks, and mitigation plans
• Experience supporting audits, inspections, and compliance activities
• Strong stakeholder communication & leadership skills
• Background in medical devices or regulated industry preferred.
Qualifications:
• Bachelor’s degree in Engineering
• 7+ years of experience (5+ years in project/site leadership).