Description
IntelliPro is seeking a contract Project Manager (Consultant) to lead the end-to-end development, testing, verification and validation, manufacturing readiness, and PMA submission of a Class III long-term implantable medical device. The role coordinates with regulatory affairs, quality, manufacturing, supply chain, and external partners; manages risks, changes, and submission timelines; and supports EU MDR transition activities. Candidates need a bachelor’s degree in a relevant technical discipline and 7–12+ years of experience managing complex medical device programs, with strong knowledge of FDA PMA submissions, design controls, and regulated manufacturing environments.
