Job description

We anticipate the application window for this opening will close on - 2 Nov 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 The Affera Mapping and Ablation System is an innovative medical technology designed to treat patients with cardiac arrhythmias. The system involves advanced mapping techniques to create detailed images of the heart's electrical activity, helping physicians identify abnormal areas causing arrhythmias. Once identified, the Affera Ablation System delivers targeted energy to disrupt these abnormal signals, restoring normal heart rhythm. This position follows Medtronic’s minimum four-day-per-week onsite work model. As a Sr. Mechanical Design Engineer in CAS Research & Technology (R&T), you will support the initial design of electrophysiology devices for use with the Affera system. This is a high impact role, defining the design direction for future catheter and sheath products.We are looking for passionate individuals who are interested in making a difference in a dynamic work environment. The ideal candidate will be a hands-on, self-starter looking to improve the lives of others through excellence in product design. Command of theoretical and practical engineering fundamental principles and an interest to learn about the field of cardiac electrophysiology are required. Primary Responsibilities: Conceptualize, prototype, design, and develop mechanical system elements of cardiac electrophysiology catheter and other Class II and III devices for high volume assembly Develop manufacturing and assembly processes for complex catheter assemblies containing miniature, precision electromechanical components. Conceptualize, design, and implement test methods and fixtures for characterization or validation Support device manufacturing efforts by developing improved processes and tooling; troubleshoot manufacturing and assembly issues. Work with Quality team members to develop recovery plans and resolve problems. Participate in design reviews and assist with Design and Process Failure Mode and Effects Analyses (FMEA). Identify and work closely with component manufacturers to ensure timely and accurate component delivery. Attend and participate in pre-clinical in-vivo system evaluations; interact with clinicians and industry professionals to evaluate design concepts. Be part of laboratory demonstrations for clinicians and internal stakeholders. Work cross-functionally with electronics hardware and software engineers to integrate electrical components and systems with the mechanical design. Required Qualifications: Bachelor s degree and a minimum of 4 years of relevant experience OR Master s degree with a minimum of 2 years relevant experience OR PhD with 0 years relevant experience. Strong design experience of mechanical products Excellent working knowledge of 3D CAD tools (SolidWorks preferred). Preferred Qualifications: . Degree focus in Mechanical Engineering Experience in medical device design a plus. Mechanical aptitude and willingness to work in a laboratory environment. Highly motivated and thrives in an environment with minimal direction. Team-oriented spirit and ability to work cross-functionally across disciplines and groups. Highly organized; strong attention to detail. Excellent written and verbal communication skills. #LI-MDT 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 . ‌ 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):$106,400.00 - $159,600.00 ‌ 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 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 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.

Requirements

Must-haves

We anticipate the application window for this opening will close on - 2 Nov 2026
This position follows Medtronic’s minimum four-day-per-week onsite work model.
Conceptualize, prototype, design, and develop mechanical system elements of cardiac electrophysiology catheter and other Class II and III devices for high volume assembly
Develop manufacturing and assembly processes for complex catheter assemblies containing miniature, precision electromechanical components.
Conceptualize, design, and implement test methods and fixtures for characterization or validation
Support device manufacturing efforts by developing improved processes and tooling; troubleshoot manufacturing and assembly issues. Work with Quality team members to develop recovery plans and resolve problems.
Participate in design reviews and assist with Design and Process Failure Mode and Effects Analyses (FMEA).
Identify and work closely with component manufacturers to ensure timely and accurate component delivery.
Attend and participate in pre-clinical in-vivo system evaluations; interact with clinicians and industry professionals to evaluate design concepts.
Be part of laboratory demonstrations for clinicians and internal stakeholders.
Work cross-functionally with electronics hardware and software engineers to integrate electrical components and systems with the mechanical design.
Bachelor s degree and a minimum of 4 years of relevant experience OR Master s degree with a minimum of 2 years relevant experience OR PhD with 0 years relevant experience.
Strong design experience of mechanical products
Degree focus in Mechanical Engineering
Mechanical aptitude and willingness to work in a laboratory environment.
Highly motivated and thrives in an environment with minimal direction.
Team-oriented spirit and ability to work cross-functionally across disciplines and groups.
Highly organized; strong attention to detail.
Excellent 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

Nice-to-haves

Excellent working knowledge of 3D CAD tools (SolidWorks preferred).
Preferred Qualifications: .
Experience in medical device design a plus.

Application prep

Use the role’s language and application details while tailoring your materials.

Platform: workday
Effort: long

Benefits

Benefits detected in the listing.

Dental

Vision

401(K)

Paid Time Off