{"schemaVersion":"jobsearcher.job.v1","id":"291bb112cd2e668b20dac990","url":"https://jobsearcher.com/jobs/291bb112cd2e668b20dac990","canonicalUrl":"https://jobsearcher.com/jobs/291bb112cd2e668b20dac990","title":"Engineering Program Manager","description":"The Product Release Program Lead is responsible for leading, establishing, and driving execution of product release cadences for the Neuromodulation and Pelvic Health (NMPH) portfolio of products. Projects within scope will include but are not limited to: Release Product Engineering (RPE), CAPAs, Sustaining Engineering, and New Product Introduction. This position requires broad cross‑functional knowledge and comprehensive business management skills.\n\nKey Skills\n\nPortfolio-wide strategy/planning for post-market product maintenance.\n\nEffective program leadership in a regulated environment plus a matrixed organization.\n\nCommunications, progress monitoring, and reporting.\n\nProduct Scope\n\nNeuromodulation and Pelvic Health (NMPH) portfolio, with a focus on TDD.\n\nKey Responsibilities\n\nProject intake & Release Planning.\n\nMonitoring and controlling in-process release projects.\n\nMaintaining effective communication (release roadmaps, schedules, release plans, proforma/budget tracker, etc.).\n\nOverall project execution: planning, budgeting, scheduling.\n\nEstablish product release strategy and operational plans.\n\nLead and manage site-specific and cross-functional teams.\n\nMonitor progress, assess risks, and implement strategies.\n\nDirect work of site-specific and cross-functional teams via a matrix organization.\n\nSecure commitments, maintain milestones and budget; deploy resources.\n\nMaintain effective communication and interface with leadership teams.\n\nEnsure proper project transition across development, quality, manufacturing, distribution, regulatory, and commercial entities.\n\nProvide input to functional managers on team member performance.\n\nAssess issues and develop resolutions to meet productivity, quality, and client‑satisfaction goals.\n\nDevelop monitoring and reporting mechanisms for project progress and intervention.\n\nEnsure compliance with all aspects of the quality policy/system.\n\nEnsure appropriate departmental resources are assigned and available.\n\nAnalyze complex, undefined problems through detailed information gathering and investigation.\n\nOther responsibilities, as required and assigned.\n\nMust Haves\n\nBachelor’s degree with 4+ years of job‑related experience -OR- Master’s degree with 2+ years of job‑related experience\n\n2+ years of project management experience\n\nNice to Haves\n\n2+ years coordinating manufacturing site activities.\n\n5+ years in medical device product development, or other highly regulated environment.\n\nProject Management Professional (PMP) certified.\n\nExperience working with FDA, ISO, EN, and/or GMP standards.\n\nHighly developed skill set in project leadership practices including ability to balance risk, effectively influence diverse teams, and ownership of responsibility for outcomes.\n\nExcellent downward, lateral, and upward communication skills.\n\nGood balance of high level strategic and detailed tactical thought processes.\n\nDemonstrated track record of successfully leading projects/programs to completion.\n\n#J-18808-Ljbffr","company":"Planet Pharma Group","rawCompany":"planet pharma group","city":"Minneapolis","state":"MN","isRemote":false,"isActive":true,"createdAt":"2026-06-20T04:44:11.490Z","occupations":[{"code":"13-1082.00","title":"Project Management Specialists","slug":"project-management-specialists"},{"code":"11-9041.00","title":"Architectural and Engineering Managers","slug":"architectural-and-engineering-managers"},{"code":"11-3051.00","title":"Industrial Production Managers","slug":"industrial-production-managers"}],"industries":[{"code":"334510","title":"Electromedical and Electrotherapeutic Apparatus Manufacturing","slug":"electromedical-and-electrotherapeutic-apparatus-manufacturing"},{"code":"339113","title":"Surgical Appliance and Supplies Manufacturing","slug":"surgical-appliance-and-supplies-manufacturing"},{"code":"325412","title":"Pharmaceutical Preparation Manufacturing","slug":"pharmaceutical-preparation-manufacturing"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Engineering Program Manager","description":"The Product Release Program Lead is responsible for leading, establishing, and driving execution of product release cadences for the Neuromodulation and Pelvic Health (NMPH) portfolio of products. Projects within scope will include but are not limited to: Release Product Engineering (RPE), CAPAs, Sustaining Engineering, and New Product Introduction. This position requires broad cross‑functional knowledge and comprehensive business management skills.\n\nKey Skills\n\nPortfolio-wide strategy/planning for post-market product maintenance.\n\nEffective program leadership in a regulated environment plus a matrixed organization.\n\nCommunications, progress monitoring, and reporting.\n\nProduct Scope\n\nNeuromodulation and Pelvic Health (NMPH) portfolio, with a focus on TDD.\n\nKey Responsibilities\n\nProject intake & Release Planning.\n\nMonitoring and controlling in-process release projects.\n\nMaintaining effective communication (release roadmaps, schedules, release plans, proforma/budget tracker, etc.).\n\nOverall project execution: planning, budgeting, scheduling.\n\nEstablish product release strategy and operational plans.\n\nLead and manage site-specific and cross-functional teams.\n\nMonitor progress, assess risks, and implement strategies.\n\nDirect work of site-specific and cross-functional teams via a matrix organization.\n\nSecure commitments, maintain milestones and budget; deploy resources.\n\nMaintain effective communication and interface with leadership teams.\n\nEnsure proper project transition across development, quality, manufacturing, distribution, regulatory, and commercial entities.\n\nProvide input to functional managers on team member performance.\n\nAssess issues and develop resolutions to meet productivity, quality, and client‑satisfaction goals.\n\nDevelop monitoring and reporting mechanisms for project progress and intervention.\n\nEnsure compliance with all aspects of the quality policy/system.\n\nEnsure appropriate departmental resources are assigned and available.\n\nAnalyze complex, undefined problems through detailed information gathering and investigation.\n\nOther responsibilities, as required and assigned.\n\nMust Haves\n\nBachelor’s degree with 4+ years of job‑related experience -OR- Master’s degree with 2+ years of job‑related experience\n\n2+ years of project management experience\n\nNice to Haves\n\n2+ years coordinating manufacturing site activities.\n\n5+ years in medical device product development, or other highly regulated environment.\n\nProject Management Professional (PMP) certified.\n\nExperience working with FDA, ISO, EN, and/or GMP standards.\n\nHighly developed skill set in project leadership practices including ability to balance risk, effectively influence diverse teams, and ownership of responsibility for outcomes.\n\nExcellent downward, lateral, and upward communication skills.\n\nGood balance of high level strategic and detailed tactical thought processes.\n\nDemonstrated track record of successfully leading projects/programs to completion.\n\n#J-18808-Ljbffr","datePosted":"2026-06-20T04:44:11.490Z","dateModified":"2026-06-20T04:44:11.490Z","hiringOrganization":{"@type":"Organization","name":"Planet Pharma Group","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Minneapolis","addressRegion":"MN","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"291bb112cd2e668b20dac990"},"url":"https://jobsearcher.com/jobs/291bb112cd2e668b20dac990"}}