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Medtronic

Senior Research & Development Engineer - Remote

Posted Yesterday
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In-Office or Remote
Hiring Remotely in State of California, USA
106K-158K Annually
Senior level
In-Office or Remote
Hiring Remotely in State of California, USA
106K-158K Annually
Senior level
Designs and analyzes scientific and engineering studies supporting cardiovascular medical device development. Develops experimental protocols, test methods, and data analyses; leads technical investigations and troubleshooting; interprets data; and communicates findings through technical documentation and presentations. Collaborates with engineering, clinical, quality, regulatory, and manufacturing teams throughout the product lifecycle, supporting preclinical studies, clinical evaluations, verification, optimization, and commercialization of technologies addressing clinical needs.
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We anticipate the application window for this opening will close on - 19 Sep 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 Cardiac Surgery Therapies (CST) Operating Unit develops technologies to support cardiac surgeons and care teams in treating cardiovascular disease. The organization partners across research, engineering, clinical, and regulatory functions to advance technologies from concept through commercialization, with a focus on improving procedural outcomes and patient care.

This position is based in San Diego, California, and is eligible for remote work within the United States. The role requires collaboration with cross-functional teams and stakeholders across multiple locations and includes up to 10% travel as needed to support project activities, team meetings, and business objectives.

The Senior Research & Development Engineer will contribute to the design, development, and advancement of cardiovascular medical technologies by applying scientific and engineering expertise to research initiatives and product development programs. This role will collaborate with cross-functional partners to investigate complex technical questions, generate data-driven insights, and translate research findings into product solutions that support clinical and commercial objectives.

Primary Responsibilities

  • Design and execute research studies to evaluate biological, physiological, or engineering questions related to product development initiatives.
  • Develop and implement experimental protocols, test methods, and data analysis approaches to support technical decision-making.
  • Lead technical investigation and troubleshooting activities to identify root causes and resolve complex product or research challenges.
  • Collaborate with cross-functional teams, including engineering, clinical, quality, regulatory, and manufacturing partners, throughout the product lifecycle.
  • Analyze and interpret experimental data and communicate findings through technical reports, presentations, and design documentation.
  • Support the development, verification, and optimization of products, processes, and technologies from concept through commercialization.
  • Contribute technical expertise to research and development programs, including activities associated with preclinical studies, clinical evaluations, or product performance assessments.
  • Translate research discoveries and technical findings into practical product solutions that address unmet clinical needs.

Required Qualifications

  • Bachelor's degree with 4+ years of relevant research and development experience, OR Master's degree with 2+ years of relevant research and development experience, OR PhD in a scientific or engineering discipline.
  • Experience designing, executing, and analyzing scientific or engineering studies in a research and development environment.
  • Experience generating technical documentation, reports, and data-driven recommendations to support product development decisions.
  • Experience collaborating with cross-functional teams to advance research, product development, or technology initiatives.

Preferred Qualifications

  • Experience within the medical device, biotechnology, life sciences, or healthcare industry.
  • Experience supporting regulated product development activities within a quality management system.
  • Knowledge of cardiovascular therapies, cardiac surgery technologies, or related clinical applications.
  • Experience with statistical analysis, experimental design, and interpretation of complex datasets.
  • Demonstrated experience contributing to the development and commercialization of new technologies or products.

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 [email protected]

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):$105,600.00 - $158,400.00


This 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 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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