Product Engineer I - Plainfield, IN

medtronic; Plainfield (IN); On-site; USD 69,000 - 103,000; Full time

Benefits offered by this job

Health, Dental and vision insurance

401(k) plan with employer match

Paid time off

Tuition assistance

Job summary

Medtronic in Plainfield, Indiana is seeking a Product Engineer I to sustain high-volume production, monitor product performance, and drive improvements across engineering activities. This entry-level role focuses on sustaining engineering, production support, and investigations to enhance quality and reliability.

The position requires a Bachelor's degree in Engineering and 0+ years of experience, with an onsite work arrangement five days per week in a manufacturing environment.

Qualifications

• Bachelor's degree in Engineering.
• 0+ years of engineering experience.

Responsibilities

• Support manufacturing operations by investigating and resolving production‑related technical issues affecting product performance, quality, and yield.
• Analyze manufacturing data to identify trends, troubleshoot process challenges, and recommend corrective actions.
• Support testing methods, procedures, and validation activities to maintain product and process performance.
• Evaluate customer returns and product‑related issues to determine root causes and recommend improvements.
• Partner with suppliers and cross‑functional teams to implement engineering changes and support component‑related investigations.
• Assist with minor product, component, or process design modifications to improve manufacturability, quality, or cost.
• Support transfer and lifecycle management activities for products and components in high‑volume production.
• Document engineering activities, investigations, and recommendations in accordance with quality system requirements.

Skills

Mechanical troubleshooting

Electrical troubleshooting

Root cause analysis

Data analysis

Cross-functional collaboration

Education

Bachelor's degree in Engineering

Job description

We anticipate the application window for this opening will close on - 11 Oct 2026

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 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 Life

This role supports product engineering activities within a medical device manufacturing environment, with a focus on sustaining high-volume production, product performance, and continuous improvement initiatives. The team partners across manufacturing, quality, operations, suppliers, and engineering functions to support device lifecycle management, production optimization, and resolution of technical issues affecting product quality and supply.

This position is based in Plainfield, Indiana and requires an onsite work arrangement five (5) days per week. Travel is not anticipated for this role.

The Product Engineer I supports commercially released products in a high-volume manufacturing environment. This entry‑level engineering role focuses on sustaining engineering activities, production support, product performance monitoring, investigation of technical issues, and implementation of engineering improvements that support quality, reliability, and operational objectives.

Primary Responsibilities

• Support manufacturing operations by investigating and resolving production‑related technical issues affecting product performance, quality, and yield.
• Analyze manufacturing data to identify trends, troubleshoot process challenges, and recommend corrective actions.
• Support testing methods, procedures, and validation activities to maintain product and process performance.
• Evaluate customer returns and product‑related issues to determine root causes and recommend improvements.
• Partner with suppliers and cross‑functional teams to implement engineering changes and support component‑related investigations.
• Assist with minor product, component, or process design modifications to improve manufacturability, quality, or cost.
• Support transfer and lifecycle management activities for products and components in high‑volume production.
• Document engineering activities, investigations, and recommendations in accordance with quality system requirements.

Required Qualifications

• Bachelor's degree in Engineering.
• 0+ years of engineering experience.

Preferred Qualifications

• Internship, co‑op, academic project, or laboratory experience in a manufacturing environment.
• Experience with mechanical and electrical troubleshooting, root cause analysis, and corrective action methodologies.
• Experience analyzing technical and manufacturing data to support process improvement and problem solving.
• Experience supporting medical device, regulated manufacturing, or other quality‑driven industries.
• Experience collaborating with cross‑functional teams to resolve technical and operational issues.

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 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.

Benefits & Compensation

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.

Salary ranges for U.S (excl. PR) locations (USD):$68,800.00 - $103,200.00

This position is eligible for a short‑term incentive called the Medtronic Incentive Plan (MIP).The base salary range is applicable across the United States, excluding Puerto Rico and specific 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 pertaining solely to candidates hired within the United States (local market compensation and benefits will apply for others)

• 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
• Simple Steps (global well‑being program)

• 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)
• 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 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 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.