{"schemaVersion":"jobsearcher.job.v1","id":"e25f293b603e818ac18b76b8","url":"https://jobsearcher.com/jobs/e25f293b603e818ac18b76b8","canonicalUrl":"https://jobsearcher.com/jobs/e25f293b603e818ac18b76b8","title":"Engineering Program Manager","description":"Job Details: Job Location: Fermatex - Jersey Shore - Wall, NJ 07727, Position Type: Full Time, Salary Range: $120,000.00 - $140,000.00 Salary/year, At DuPont, our purpose is to empower the world with essential innovations to thrive. We work on things that matter. Whether it's providing clean water to more than a billion people on the planet, producing materials that are essential in everyday technology devices from smartphones to electric vehicles, or protecting workers around the world. Discover the many reasons the world's most talented people are choosing to work at DuPont.\nThis role leads product development and commercialization programs that advance strategic growth objectives, guiding cross-functional teams through the New Product Commercialization Framework (NPCF) to deliver innovative, compliant, and manufacturable medical device solutions from opportunity assessment through commercial launch.\nESSENTIAL DUTIES: Lead programs through all phases of the New Product Commercialization Framework (NPCF-Global and NPCF-Lite projects), from opportunity assessment through commercial launch, ensuring achievement of program objectives, timelines, and business outcomes.\nServe as the primary program leader and cross-functional coordinator, aligning engineering, operations, quality, regulatory, supply chain, commercial, and customer stakeholders to execute strategic program objectives.\nDevelop and maintain integrated program plans, including scope, schedule, budget, resources, risks, and critical deliverables, ensuring proactive management of program performance.\nBuild and maintain trusted customer relationships, positioning the organization as a strategic development and manufacturing partner for medical device OEMs.\nLead program governance activities, including Stage Gate Reviews, executive updates, and steering committee presentations, ensuring informed decision making and adherence to Stage Gate requirements.\nDrive risk identification, mitigation planning, and issue resolution through active management of program risk registers, escalations, and contingency plans.\nEnsure compliance with applicable quality, regulatory, and design control requirements, including design inputs, design outputs, verification, validation, and production transfer activities.\nManage program financial performance, including development revenue, non-recurring engineering (NRE), budget accountability, scope management, purchase order coverage, and forecasting.\nLead commercialization and technology transfer activities to support sustainable, efficient, repeatable, and scalable manufacturing operations across global sites.\nSupport business growth through participation in customer strategy discussions, opportunity assessments, establishing business cases, and development of program execution strategies.\nCommunicate program status, risks, financial performance, and key decisions clearly and effectively to customers, leadership teams, and internal stakeholders.\nChampion continuous improvement initiatives that enhance commercialization effectiveness, project execution, customer experience, and organizational capability.\nUpholds core values designed to support our commitment to driving growth and continuous improvement:\nWe put safety and respect first\nWe act with integrity and accountability\nWe grow and improve every day\nWe solve problems for customers.\nQualifications: Bachelor's degree in Engineering, Life Sciences, Business, or a related technical discipline.\nPMP (Project Management Professional) certification required.\n10+ years of experience leading complex product development, commercialization, or manufacturing programs within a regulated industry.\nDemonstrated expertise in new product development, design controls, technology transfer, and commercialization processes.\nProven ability to lead cross-functional teams and influence stakeholders across engineering, operations, quality, regulatory, supply chain, commercial, and customer organizations without direct authority.\nStrong understanding of program management disciplines, including scope, schedule, resource planning, risk management, financial management, and stage-gate governance.\nExperience managing program financial performance, including budgets, forecasting, business cases, development revenue, and resource planning.\nWorking knowledge of ISO 13485, medical device design controls, and regulated product development requirements.\nExperience in medical device contract design, development, or manufacturing environments.\nAbility and willingness to work primarily onsite, preferably in Minneapolis, to facilitate cross-functional collaboration, customer engagement, and program execution.\nWORKING CONDITIONS: Works with minimal supervision from manager. Requires light physical activity performing non-strenuous daily activities.\nNOTE: This job description is not intended to be an exhaustive list of all possible duties, responsibilities and or qualifications. Other duties, responsibilities and/or qualifications may be assigned to this position.\n\n#J-18808-Ljbffr","company":"Spectrum Plastics Group","rawCompany":"spectrum plastics group","city":"Wall","state":"SD","isRemote":false,"isActive":true,"createdAt":"2026-10-11T03:34:52.469Z","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":"11-9121.00","title":"Natural Sciences Managers","slug":"natural-sciences-managers"}],"industries":[{"code":"541715","title":"Research and Development in the Physical, Engineering, and Life Sciences (except Nanotechnology and Biotechnology)","slug":"research-and-development-in-the-physical-engineering-and-life-sciences-except-nanotechnology-and-biotechnology"},{"code":"334510","title":"Electromedical and Electrotherapeutic Apparatus Manufacturing","slug":"electromedical-and-electrotherapeutic-apparatus-manufacturing"},{"code":"541330","title":"Engineering Services","slug":"engineering-services"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Engineering Program Manager","description":"Job Details: Job Location: Fermatex - Jersey Shore - Wall, NJ 07727, Position Type: Full Time, Salary Range: $120,000.00 - $140,000.00 Salary/year, At DuPont, our purpose is to empower the world with essential innovations to thrive. We work on things that matter. Whether it's providing clean water to more than a billion people on the planet, producing materials that are essential in everyday technology devices from smartphones to electric vehicles, or protecting workers around the world. Discover the many reasons the world's most talented people are choosing to work at DuPont.\nThis role leads product development and commercialization programs that advance strategic growth objectives, guiding cross-functional teams through the New Product Commercialization Framework (NPCF) to deliver innovative, compliant, and manufacturable medical device solutions from opportunity assessment through commercial launch.\nESSENTIAL DUTIES: Lead programs through all phases of the New Product Commercialization Framework (NPCF-Global and NPCF-Lite projects), from opportunity assessment through commercial launch, ensuring achievement of program objectives, timelines, and business outcomes.\nServe as the primary program leader and cross-functional coordinator, aligning engineering, operations, quality, regulatory, supply chain, commercial, and customer stakeholders to execute strategic program objectives.\nDevelop and maintain integrated program plans, including scope, schedule, budget, resources, risks, and critical deliverables, ensuring proactive management of program performance.\nBuild and maintain trusted customer relationships, positioning the organization as a strategic development and manufacturing partner for medical device OEMs.\nLead program governance activities, including Stage Gate Reviews, executive updates, and steering committee presentations, ensuring informed decision making and adherence to Stage Gate requirements.\nDrive risk identification, mitigation planning, and issue resolution through active management of program risk registers, escalations, and contingency plans.\nEnsure compliance with applicable quality, regulatory, and design control requirements, including design inputs, design outputs, verification, validation, and production transfer activities.\nManage program financial performance, including development revenue, non-recurring engineering (NRE), budget accountability, scope management, purchase order coverage, and forecasting.\nLead commercialization and technology transfer activities to support sustainable, efficient, repeatable, and scalable manufacturing operations across global sites.\nSupport business growth through participation in customer strategy discussions, opportunity assessments, establishing business cases, and development of program execution strategies.\nCommunicate program status, risks, financial performance, and key decisions clearly and effectively to customers, leadership teams, and internal stakeholders.\nChampion continuous improvement initiatives that enhance commercialization effectiveness, project execution, customer experience, and organizational capability.\nUpholds core values designed to support our commitment to driving growth and continuous improvement:\nWe put safety and respect first\nWe act with integrity and accountability\nWe grow and improve every day\nWe solve problems for customers.\nQualifications: Bachelor's degree in Engineering, Life Sciences, Business, or a related technical discipline.\nPMP (Project Management Professional) certification required.\n10+ years of experience leading complex product development, commercialization, or manufacturing programs within a regulated industry.\nDemonstrated expertise in new product development, design controls, technology transfer, and commercialization processes.\nProven ability to lead cross-functional teams and influence stakeholders across engineering, operations, quality, regulatory, supply chain, commercial, and customer organizations without direct authority.\nStrong understanding of program management disciplines, including scope, schedule, resource planning, risk management, financial management, and stage-gate governance.\nExperience managing program financial performance, including budgets, forecasting, business cases, development revenue, and resource planning.\nWorking knowledge of ISO 13485, medical device design controls, and regulated product development requirements.\nExperience in medical device contract design, development, or manufacturing environments.\nAbility and willingness to work primarily onsite, preferably in Minneapolis, to facilitate cross-functional collaboration, customer engagement, and program execution.\nWORKING CONDITIONS: Works with minimal supervision from manager. Requires light physical activity performing non-strenuous daily activities.\nNOTE: This job description is not intended to be an exhaustive list of all possible duties, responsibilities and or qualifications. Other duties, responsibilities and/or qualifications may be assigned to this position.\n\n#J-18808-Ljbffr","datePosted":"2026-10-11T03:34:52.469Z","dateModified":"2026-10-11T03:34:52.469Z","hiringOrganization":{"@type":"Organization","name":"Spectrum Plastics Group","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Wall","addressRegion":"SD","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"e25f293b603e818ac18b76b8"},"url":"https://jobsearcher.com/jobs/e25f293b603e818ac18b76b8"}}