Medical Device Program Management

Title: Medical Device Program Management (FDA / ISO 13485 environment)Location: Greater Merrimack Area, NH (Hybrid 3 days onsite)Employment Type: ContractStatus: Accepting CandidatesOverview Seeking an experienced Operations Program Manager to support build-to-print and sustaining activities for complex products in an FDA-regulated environment. This role will lead transition and sustaining programs, coordinate cross-functional teams, and ensure continuity of supply across the product lifecycle.Key ResponsibilitiesAct as primary customer interface for operations, production commitments, and PO coverageLead sustaining engineering, product transition, and lifecycle management projectsCoordinate cross-functional work across Engineering, Supply Chain, Procurement, and OperationsMaintain product portfolio roadmap and support new product introduction activitiesDrive continuity of supply, cost reduction, and operational readinessPrepare project status reports and support business reviews and steering meetingsQualificationsBachelor’s degree in Engineering and/or OperationsExperience with medical devices in an FDA-regulated environmentProven program management experience with electro-mechanical or instrumentation productsExperience supporting product transfer, sustaining, or lifecycle programsFamiliarity with ISO 13485 and regulatory compliance requirements#J-18808-Ljbffr