Engineering Program Manager

Careers 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 95000 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.

As an Engineering Program Manager within Medtronics Advanced Manufacturing Engineering (AME) team you will lead cross-functional engineering programs that support the development industrialization and launch of innovative medical technologies. Working across Engineering Manufacturing Quality Operations Supply Chain and external partners youll help transform new ideas into scalable manufacturing solutions that improve patient outcomes worldwide.

This is a fully onsite position based in Danvers MA where in-person collaboration is essential to supporting our AME development teams and delivering life-changing therapies.

Responsibilities may include:

• Lead engineering programs supporting new product development manufacturing readiness and technology transfer.
• Develop and manage project plans schedules budgets resources and risk mitigation strategies.
• Guide engineering activities from concept through commercialization.
• Partner cross-functionally to ensure projects are delivered on time within scope and aligned with business objectives.
• Evaluate and implement new manufacturing technologies processes equipment and engineering solutions.
• Lead technical feasibility assessments and support process development and continuous improvement initiatives.
• Ensure engineering documentation and technical quality requirements are maintained throughout the product lifecycle.
• Coordinate activities with suppliers consultants and external partners to meet program objectives.
• Monitor program performance resolve technical challenges and communicate progress to key stakeholders.
• Mentor engineering talent and foster collaboration innovation and operational excellence.

Required Qualifications

• Bachelors degree with minimum of 5 years of related experience OR
• Masters degree with a minimum of 3 years of related experience

Preferred Qualifications

• 7 years of engineering manufacturing engineering product development or technical program management experience.
• Experience leading complex cross-functional engineering projects.
• Strong project management communication and problem-solving skills.
• Experience supporting medical device product development and commercialization.
• Knowledge of Design Controls FDA Quality System Regulations ISO 13485 or other regulated product development frameworks.
• Experience with manufacturing automation process development equipment validation or Advanced Manufacturing Engineering.
• Experience leading technology transfers process scale-up or manufacturing readiness initiatives.
• PMP Agile Lean Six Sigma or similar project management/process improvement certification.
• Strong analytical and problem-solving abilities with a data-driven decision-making approach.
• Demonstrated ability to influence without direct authority and build strong cross-functional partnerships.

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 Requirements

The 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 & Sponsorship

At Medtronic we are committed to fostering an environment where employees can thrive and make a meaningful 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.

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Apply only through official Medtronic channels. All legitimate Medtronic recruiting communications come from approved Medtronic platforms and official @ email addresses.

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Medtronic offers a competitive Salary and flexible Benefits Package
A 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.

The following benefits and additional compensation are available to those regular employees who work 20 hours per week: Health Dental and vision insuranceHealth Savings AccountHealthcare Flexible Spending AccountLife insurance Long-term disability leaveDependent daycare spending accountTuition assistance/reimbursement andSimple 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 matchShort-term disabilityPaid time offPaid holidaysEmployee Stock Purchase PlanEmployee Assistance ProgramNon-qualified Retirement Plan Supplement (subject to IRS earning minimums) andCapital 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 plans

It 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 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 findhere 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.