Engineering Program Manager

Paycom - ATS; Minneapolis (MN); On-site; USD 120,000 - 140,000; Full time

Job summary

DuPont is seeking a Senior Program Manager to lead complex medical device development and commercialization programs in a regulated environment, onsite in Minneapolis.

You will align cross-functional teams across engineering, operations, quality, regulatory, supply chain and commercial to meet objectives, manage budgets, and drive Stage-Gate governance and risk mitigation.

Qualifications

• Bachelor's degree in Engineering, Life Sciences, Business, or related technical discipline.
• PMP (Project Management Professional) certification.
• 10+ years of experience leading complex product development, commercialization, or manufacturing programs in a regulated industry.
• Experience in new product development, design controls, technology transfer, and commercialization processes.
• Proven ability to lead cross-functional teams and influence stakeholders without direct authority.
• Knowledge of ISO 13485 and regulated product development requirements.
• Willingness to work onsite in Minneapolis.

Responsibilities

• Lead programs through all phases of NPCF from opportunity assessment to commercial launch.
• Serve as primary program leader coordinating engineering, operations, quality, regulatory, supply chain, commercial, and customer stakeholders.
• Develop and maintain integrated program plans including scope, schedule, budget, resources, risks, and deliverables.
• Build and maintain relationships with medical device OEMs.
• Lead governance activities including Stage Gate Reviews and executive updates.
• Drive risk identification, mitigation, and issue resolution.
• Ensure compliance with quality, regulatory, and design controls; oversee design inputs/outputs, validation, and production transfer.
• Manage program financial performance including budgets, revenue, and forecasting.
• Lead commercialization and technology transfer across global sites.
• Support business growth through customer strategy discussions and development of execution strategies.
• Communicate status, risks, and key decisions to customers and leadership.
• Champion continuous improvement initiatives.

Skills

Cross-functional leadership

Stakeholder management

Regulated industry experience

Education

Bachelor's degree in Engineering, Life Sciences, Business, or a related technical discipline

PMP (Project Management Professional) certification

Job description

Job Details

Job Location: SPG - Minneapolis - Minneapolis , MN 55426, 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.

ESSENTIAL 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.
• Serve 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.
• Develop and maintain integrated program plans, including scope, schedule, budget, resources, risks, and critical deliverables, ensuring proactive management of program performance.
• Build and maintain trusted customer relationships, positioning the organization as a strategic development and manufacturing partner for medical device OEMs.
• Lead program governance activities, including Stage Gate Reviews, executive updates, and steering committee presentations, ensuring informed decision making and adherence to Stage Gate requirements.
• Drive risk identification, mitigation planning, and issue resolution through active management of program risk registers, escalations, and contingency plans.
• Ensure compliance with applicable quality, regulatory, and design control requirements, including design inputs, design outputs, verification, validation, and production transfer activities.
• Manage program financial performance, including development revenue, non-recurring engineering (NRE), budget accountability, scope management, purchase order coverage, and forecasting.
• Lead commercialization and technology transfer activities to support sustainable, efficient, repeatable, and scalable manufacturing operations across global sites.
• Support business growth through participation in customer strategy discussions, opportunity assessments, establishing business cases, and development of program execution strategies.
• Communicate program status, risks, financial performance, and key decisions clearly and effectively to customers, leadership teams, and internal stakeholders.
• Champion continuous improvement initiatives that enhance commercialization effectiveness, project execution, customer experience, and organizational capability.

Upholds core values designed to support our commitment to driving growth and continuous improvement

• We put safetyand respectfirst
• We act with integrityand accountability
• We growand improveevery day
• We solve problemsfor customers.

Follows all safety guidelines and adheres to safety absolutes.

Qualifications

• Bachelor's degree in Engineering, Life Sciences, Business, or a related technical discipline.
• PMP (Project Management Professional) certification required.
• 10+ years of experience leading complex product development, commercialization, or manufacturing programs within a regulated industry.
• Demonstrated expertise in new product development, design controls, technology transfer, and commercialization processes.
• Proven ability to lead cross-functional teams and influence stakeholders across engineering, operations, quality, regulatory, supply chain, commercial, and customer organizations without direct authority.
• Strong understanding of program management disciplines, including scope, schedule, resource planning, risk management, financial management, and stage-gate governance.
• Experience managing program financial performance, including budgets, forecasting, business cases, development revenue, and resource planning.
• Working knowledge of ISO 13485, medical device design controls, and regulated product development requirements.
• Experience in medical device contract design, development, or manufacturing environments.
• Ability and willingness to work primarily onsite, preferably in Minneapolis, to facilitate cross-functional collaboration, customer engagement, and program execution.

WORKING CONDITIONS

Works with minimal supervision from manager. Requires light physical activity performing non-strenuous daily activities.

NOTE

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.