DuPont is seeking an experienced Project Manager to lead high-impact initiatives in a regulated medical device manufacturing environment. The role brings together Operations, Engineering, Quality, Regulatory Affairs, Supply Chain, R&D, Finance, and external partners to deliver manufacturing projects from concept through implementation and closeout. The Project Manager is accountable for scope, schedule, budget, risk, quality, and stakeholder alignment across projects that may include technology transfers, process validation, equipment installation and qualification, automation, facility upgrades, cost reduction, and capacity expansion. The position involves coordinating manufacturing readiness and working closely with Quality and Regulatory teams to maintain compliance with cGMP, ISO 13485, applicable FDA requirements, change-control processes, validation requirements, and internal procedures. The successful candidate will help ensure projects are handed off sustainably, with trained teams, controlled documentation, completed validation requirements, and clear long-term ownership. DuPont describes its compensation and benefits package as comprehensive; further details are available through its Compensation and Benefits page.
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Job Type
Full-time
Career Level
Mid Level