Save Job Back to Search Job Description Summary Similar JobsDo you have experience leading programs for complex medical devices?Great opportunity to lead end-to-end new product development!About Our ClientMy client is a world leader for Class III medical devices. This is an exciting time to join the company as they are growing considerably right now and are working on expanding their product lines!Job DescriptionThe Program Manager will:Lead end‑to‑end execution of complex new product development programs spanning capital equipment, disposable components, and software‑enabled systemsDevelop and manage comprehensive program plans, including scope, schedules, budgets, resources, and risk management strategiesCreate and maintain detailed program schedules (Gantt charts, WBS), identify critical paths and interdependencies, and proactively mitigate timeline risksCoordinate cross‑functional teams across R&D, Quality, Regulatory, Clinical, Operations, and Commercial to achieve program objectivesManage integration and dependencies across hardware, disposable, and software development workstreams to ensure aligned executionOversee design control activities, ensuring documentation completeness, traceability, and regulatory readinessManage external vendor and partner relationships, including software providers, contract manufacturers, and testing partnersServe as the primary point of contact for program communication, delivering clear status updates to senior leadership and key stakeholdersFacilitate phase‑gate reviews and ensure deliverables meet quality system and regulatory requirementsTrack and report program metrics, proactively escalate risks or issues, and drive timely resolutionApply today for immediate consideration!MPI does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity or expression, national origin, age, disability, veteran status, marital status, or based on an individual's status in any group or class protected by applicable federal, state or local law. MPI encourages applications from minorities, women, the disabled, protected veterans and all other qualified applicants.The Successful ApplicantThe successful Program Manager will have the following qualifications:Bachelor's degree in Engineering, Life Sciences, or a related technical field, MAster's degree of MBA is prefered5+ years of program or project management experience within the medical device, biotech, or pharmaceutical industryDemonstrated experience managing full product lifecycle programs, including design controls and regulatory submissionsProven ability to lead cross‑functional teams and deliver FDA‑regulated productsStrong working knowledge of quality systems and regulatory requirements (FDA, ISO, EU MDR, etc.)Experience supporting Class II or Class III medical devicesBackground in systems engineering or integration of hardware and software platformsFamiliarity with clinical trial planning and executionWorking knowledge of risk management (ISO 14971), usability engineering, and design verification/validation (V&V)What's on OfferCompetitive compensationComprehensive benefits package401K with company matchFull health insurance including medical, dental and visionGenerous PTO11 paid holidaysGreat company culture and room for growth!ContactBrittany SchumannQuote job refJN-042026-7001562Job summarySectorEngineering & ManufacturingSub SectorEngineering Design and R&DIndustryIndustrial / ManufacturingLocationWakefieldContract TypePermanentConsultant nameBrittany SchumannJob ReferenceJN-042026-7001562