Senior Engineering Program Manager - Onsite

Medtronic plc; Minneapolis (MN); On-site; USD 171,000 - 257,000; Full time

Benefits offered by this job

Health, Dental and Vision Insurance

401(k) Plan with employer match

Tuition assistance/reimbursement

Paid time off

Job summary

Medtronic plc in Minneapolis is seeking a Senior Engineering Program Manager within the Pelvic Health Operating Unit. You will lead cross-functional operations activities that support new product introductions, manufacturing readiness, and supply chain preparedness, ensuring quality compliance and successful transfer of products into commercial production.

The role coordinates design transfer, process validation, and launch builds across manufacturing value streams while managing schedule,

Qualifications

• Experience leading cross-functional product development and new product introduction programs.
• Experience working in regulated industries with quality systems.
• Ability to manage project schedules, risks, budgets, and operational performance metrics.
• Knowledge of medical device regulations and design history files (DHF).

Responsibilities

• Lead cross-functional Operations teams to deliver new product introduction milestones, manufacturing readiness, and commercialization objectives.
• Represent Operations as the primary interface to product development core teams and ensure operational requirements are incorporated into program decisions.
• Develop and manage operations project plans, timelines, budgets, dependencies, risks, and performance metrics throughout the product development lifecycle.
• Define manufacturing and supply chain strategies, including site selection, capacity planning, and contract manufacturing scope.
• Drive completion of design transfer activities, manufacturing scale-up plans, validation strategies, and operational deliverables for product launch.

Skills

Cross-functional leadership

Project management

Regulated environments

Quality systems knowledge

Stakeholder influence

Education

Bachelor's degree in Engineering/related field

Master's degree in Engineering/Operations/Business

Tools

PMP certification

DFSS

Lean Manufacturing

DFMA

Design for Reliability

Job description

We anticipate the application window for this opening will close on - 7 Nov 2026Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to put patients first — developing innovative medical technologies that improve the lives of 72+ million patients each year. Your unique talents will help shape the future of healthcare while building a career grounded in purpose, growth, and impact.A Day in the LifeThe Pelvic Health Operating Unit develops therapies that help patients manage conditions affecting bladder and bowel control through implantable neuromodulation technologies. We work closely with product development, manufacturing, quality, supply chain, and regulatory teams to launch new products and maintain a reliable global manufacturing network.Check us out on LinkedIn: Medtronic Pelvic Health .This position is based in Minneapolis, Minnesota, and follows an onsite work arrangement. The role partners with global cross-functional teams and manufacturing sites to drive operational readiness and execution for new product introductions. Travel is not required for this position.The Senior Engineering Program Manager serves as the Core Team Operations Representative (CTOR) and primary Operations interface to product development teams within the Pelvic Health Operating Unit. This role is responsible for leading cross-functional operations activities that support new product introduction programs, ensuring manufacturing readiness, supply chain preparedness, quality compliance, and the successful transfer of products into commercial production. This role aligns operations, manages schedule, risk, cost, capacity, and execution across the product development lifecycle.Primary ResponsibilitiesLead cross-functional Operations teams to deliver new product introduction milestones, manufacturing readiness, and commercialization objectives.Represent Operations as the primary interface to product development core teams and ensure operational requirements are incorporated into program decisions.Develop and manage operations project plans, timelines, budgets, dependencies, risks, and performance metrics throughout the product development lifecycle.Define manufacturing and supply chain strategies, including site selection, make-versus-buy decisions, capacity planning, contract manufacturing scope, and business continuity considerations.Drive completion of design transfer activities, manufacturing scale-up plans, validation strategies, and operational deliverables required for product launch.Coordinate development and launch builds across manufacturing value streams while monitoring schedule performance, yield targets, and operational risks.Ensure compliance with quality system requirements, design history documentation, and regulatory submission support related to operations activities.Apply Design for Reliability, Design for Manufacturability, Lean Manufacturing, Design for Six Sigma, and related methodologies to improve product and process performance.Required QualificationsBachelor's degree with 7+ years of engineering, operations, manufacturing, supply chain, or program management experience OR Master's degree with 5+ years of engineering, operations, manufacturing, supply chain, or program management experience.Experience leading cross-functional projects involving product development, manufacturing transfer, or new product introduction.Experience managing project schedules, risks, budgets, and operational performance metrics.Experience working within regulated industries and quality management systems.Experience influencing stakeholders and leading matrixed teams without direct authority.Preferred QualificationsExperience serving as a Core Team Operations Representative (CTOR) or operations lead for medical device product development programs.Experience with manufacturing process validation, capacity planning, and design transfer activities.Experience applying Design for Six Sigma (DFSS), Lean Manufacturing, Design for Manufacturability and Assembly (DFMA), or Reliability Engineering methodologies.Knowledge of medical device regulations, Design History Files, and commercialization requirements.Project Management Professional (PMP) certification and/or advanced degree in Engineering, Operations, Supply Chain, or Business.For Baccalaureate degrees earned outside of the United States, a degree that satisfies the requirements of 8 C.F.R. § 214.2(h)(4)(iii)(A) is required.Physical Job RequirementsThe above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position.The physical demands described within the Responsibilities section of this job description are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. For Office Roles: While performing the duties of this job, the employee is regularly required to be independently mobile. The employee is also required to interact with a computer, and communicate with peers and co-workers. Contact your manager or local HR to understand the Work Conditions and Physical requirements that may be specific to each role.U.S. Work Authorization & SponsorshipAt Medtronic, we are committed to fostering an environment where employees can thrive and make a meaningful impact. In alignment with our enterprise-wide workforce planning approach, U.S. work authorization sponsorship (H-1B, TN, J, etc.) is offered exclusively for Principal-level roles and above, where specialized expertise aligns with long-term business needs. Roles below the Principal level require candidates to possess unrestricted U.S. work authorization at the time of hire and for the duration of employment.Recruitment Fraud AlertWe are aware of phishing scams targeting job seekers. Please keep the following in mind:Apply only through official Medtronic channels. All legitimate Medtronic recruiting communications come from approved Medtronic platforms and official @medtronic.com email addresses.Medtronic will never ask for payment or sensitive personal information (such as bank account or Social Security details) during early stages of the hiring process. Any such requests are not legitimate.If you receive a suspicious message claiming to be from Medtronic, do not respond, click links, or open attachments.If you have any questions, concerns regarding the authenticity of a communication alleged to have been made by or on behalf of Medtronic, please contact us immediately at [e-mail] .Benefits & CompensationMedtronic offers a competitive Salary and flexible Benefits PackageA commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.Salary ranges for U.S (excl. PR) locations (USD):$171,200.00 - $256,800.00This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).The base salary range applies across the United States, excluding Puerto Rico and certain locations in California. The offered rate complies with federal and local regulations and may vary based on factors such as experience, certification/education, market conditions, and location. Compensation and benefits information pertains solely to candidates hired within the United States (local market compensation and benefits will apply for others).The following benefits and additional compensation are available to those regular employees who work 20+ hours per week: Health, Dental and vision insurance , Health Savings Account , Healthcare Flexible Spending Account , Life insurance, Long-term disability leave , Dependent daycare spending account , Tuition assistance/reimbursement , and Simple Steps (global well-being program).The following benefits and additional compensation are available to all regular employees: Incentive plans, 401(k) plan plus employer contribution and match , Short-term disability , Paid time off , Paid holidays , Employee Stock Purchase Plan , Employee Assistance Program , Non-qualified Retirement Plan Supplement (subject to IRS earning minimums) , and Capital Accumulation Plan (available to Vice Presidents and above, or subject to IRS earning minimums).Regular employees are those who are not temporary, such as interns. Temporary employees are eligible for paid sick time, as required under applicable state law, and the Employee Stock Purchase Plan. Please note some of the above benefits may not apply to workers in Puerto Rico.Further details are available at the link below:Medtronic benefits and compensation plansIt is the policy of Medtronic to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Medtronic will provide reasonable accommodations for qualified individuals with disabilities.If you are applying to perform work for Medtronic, Inc. (“Medtronic”) in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can find here a list of all material job duties of the specific job position which Medtronic reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment. Medtronic will consider for employment qualified job applicants with arrest or conviction records in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act.