Medtronic
MEDICAL DEVICES
Medical Devices
LocationNJ - Phillipsburg
Open Jobs1071
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Design Quality Engineer I
Medtronic
This listing was originally posted on Medtronic's careers page. Formulate is an equal opportunity job aggregator and is not involved in the hiring process. Where salary information is estimated, it is derived from BLS industry benchmarks and may differ from actual compensation.
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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.
Our Medtronic Surgical team is working to bring the benefits of minimally invasive surgery (MIS) to more people and places through a portfolio of robotic and digital solutions. Together, we are working to broaden options and expand access globally for hospitals, surgeons, and patients.
As a Design Quality Engineer I, you will play a critical role supporting the design quality, risk management, and U.S. launch of innovative surgical robotics systems, capital equipment, and instrumentation, including the Hugo™ platform.
This design-focused quality role works at the intersection of R&D, manufacturing, supplier quality, and regulatory, supporting medical device designs from early development through manufacturing transfer and post-launch support.
You will translate design and risk requirements into effective manufacturing controls, ensuring quality is built into the product from the outset, with a specific focus on hardware systems, electrical safety, and capital equipment performance in the field, while operating with a high degree of autonomy and cross-functional influence.
Key Responsibilities
Lead and support design quality and risk management activities, including DFMEA development and cross‑functional risk reviews
Own and maintain elements of the Product Risk Management File throughout the product lifecycle
Partner with R&D to embed quality and risk controls into system, hardware, and design requirements
Translate design and CTQ requirements into robust manufacturing controls and inspection strategies, including hardware performance and safety requirements
Collaborate with manufacturing teams to support design transfer, production readiness, and issue resolution
Support supplier qualification and supplier quality activities, including design‑related inputs
Support design quality activities for capital equipment and electromechanical systems, including hardware integration and system-level considerations
Contribute to electrical safety and compliance activities (e.g., IEC 60601), including risk identification and test strategy alignment
Partner with cross-functional teams to ensure serviceability, reliability, and field maintenance considerations are incorporated into product design
Perform quality testing, statistical analysis, and root-cause investigations to address nonconformances and CAPAs
Participate in design reviews, change management, and technical decision-making
Support complaint investigations, post-market activities, and U.S. launch hyper-care efforts
Required Qualifications
Bachelor’s degree in Electrical Engineering, Biomedical Engineering, or a related hardware-focused technical discipline
Preferred Qualifications
Experience working with capital equipment or complex electromechanical medical devices
Familiarity with IEC 60601 or other electrical safety standards
Experience with hardware systems, PCBAs, or electromechanical components
1-3 years of experience in Electrical Engineering, Quality Engineering, Design Quality, Manufacturing Quality, or related roles
Background in a regulated industry (medical devices strongly preferred; robotics, capital equipment, or aerospace highly relevant)
Hands-on experience with design risk management, including DFMEA
Experience working cross-functionally with manufacturing teams and suppliers
Experience supporting U.S. product launches, post-market surveillance, complaints, and/or CAPAs
Familiarity with statistical analysis tools (e.g., Minitab, JMP)
Prior exposure to manufacturing or operations environments
Exposure to serviceability, field support, or equipment maintenance considerations in product design
Ability to work independently, manage priorities, and influence without direct authority
Strong written and verbal communication skills
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.
Recruitment Fraud Alert
We 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 AskHR@medtronic.com.
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.
This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).
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 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.
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MEDICAL DEVICES
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