Senior R&D Engineer

MiniMed; Los Angeles (CA); On-site; USD 97,000 - 165,000; Full time

Job summary

MiniMed is seeking an experienced Failure Analysis lead within the CGM Sensor R&D team in Los Angeles, CA. You will lead failure analyses across development phases, interfacing with regulatory, quality, reliability, and clinical teams to identify root causes and guide corrective actions.

The role requires a bachelor’s degree with 4+ years of relevant experience, or an advanced degree with 2+ years. You will contribute to sustaining and improving CGM technologies and product quality.

Qualifications

• Requires a Bachelor’s degree and minimum of 4 years of relevant experience, or an advanced degree with a minimum of 2 years relevant experience.

Responsibilities

• Troubleshooting and identifying the root cause of failures in complex microfabricated electrochemical bio-sensors.
• Develop, record, and perform various failure analyses to determine failure mechanisms and root causes.
• Write formal analysis reports with clear messaging about analysis findings to stakeholders.
• Collaborate with technicians and other R&D engineers to assess failures and opportunities for product improvements.
• Lead continuous improvement efforts and implement corrective actions in development stages.
• Develop new test methodologies to aid in failure analysis of components and products.
• Research and analyze failures in early product development stages to improve quality and reliability.
• Conduct hands-on lab work and define failure analysis strategy across development phases.

Education

Bachelor's degree

Advanced degree

Job description

We anticipate the application window for this opening will close on - 29 Sep 2026

At MiniMed, you can begin a lifelong career of exploration and innovation, while helping make a difference in the lives of people living with diabetes around the globe. You'll lead with purpose, breaking down barriers to innovation for a more connected, compassionate world.

About The Role

This position is within the Continuous Glucose Monitoring (CGM) Sensor R&D team. In this role, you will be supporting the development of next generation CGM products and sustaining R&D. You will be responsible for leading the Failure Analysis efforts throughout different phases of sensor product development while contributing towards sustaining, continuous improvement, and development activities.

In this role, the individual will be interfacing with other R&D functions, regulatory, quality, reliability, and clinical teams as appropriate.

Responsibilities may include the following and other duties may be assigned.

• Troubleshooting and identifying the root cause of failures in complex microfabricated electrochemical bio-sensors
• Develop, record, and perform various failure analyses on systems and components to determine failure mechanisms and ultimately root causes of failure
• Write formal analysis reports, resulting in clear and accurate messaging about analysis findings to both the submitter and a broader audience
• Use working knowledge of failure modes of products to work with technicians and other R&D engineers to assess existing and potential failures
• Work with R&D and quality engineers to identify opportunities for improvements in product quality, reliability, manufacturability, and functionality
• Initiates and leads the efforts on implementing improvements identified as a part of continuous improvement
• Obtain, interpret, and utilize data from formal test, complaint handling, and other document repositories
• Develop new test methodologies to aid in the failure analysis of components and products
• Identify and research component & system failures in the early stages of product development to improve product quality and reliability
• Conduct hands‑on lab work, define failure analysis strategy, and recommend corrective actions/fixes to failures at different phases of product development
• Development of analytical methodologies and equipment acquisitions to ensure strategic failure analysis capabilities for future technologies and products
• Contribute to development of continuous glucose monitoring subsystems as relevant to the group goals.

Required Knowledge And Experience

Requires a Bachelors degree and minimum of 4 years of relevant experience, or advanced degree with a minimum of 2 years relevant experience.

Preferred Qualifications

• Masters of Science Degree in Biomedical Engineering, Chemical Engineering or related Engineering field with 5+ years of professional experience.
• Medical Device Industry Experience.
• Experience in product design and development in an R&D environment.
• Experience in mechanical and/or electrochemical systems.
• Direct experience in characterization, design of experiments and data analysis methodologies (T-test, ANOVA and significance testing at a minimum)
• Knowledge about in‑vitro and in‑vivo testing of subcutaneous medical devices.

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.

Benefits & Compensation

MiniMed offers a competitive salary and flexible benefits package

At MiniMed, we put people first. A commitment to our employees lives at the core of our values: We recognize their contributions. They share in the success they help create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every stage of your career and life.

Salary ranges for U.S (excl. PR) locations (USD):$87,000.00 - $149,000.00

For roles located in California, Seattle WA, Washington DC, Boston MA, and New York City, the salary range is $97,000.00 - $165,000.00 USD.

Actual compensation may vary based on factors including experience, education, certifications, skills, market conditions, internal equity, and geographic location. Compensation and benefits information pertains solely to candidates hired within the United States (local market compensation and benefits will apply for others).

This position is eligible for a short-term incentive called the Short Term Incentive (STI).

At MiniMed, we are committed to supporting the well‑being and financial security of our employees. Regular employees working 20 or more hours per week are eligible for a robust benefits package, including health, dental, and vision insurance, as well as access to a Health Savings Account, Healthcare Flexible Spending Account, life insurance, long‑term disability leave, and a dependent daycare spending account. In addition, all regular employees enjoy incentive plans, a 401(k) plan with company match, short‑term disability coverage, paid time off and holidays, participation in our Employee Stock Purchase Plan, and access to our Employee Assistance Program. Eligible employees may also benefit from our Non‑qualified Retirement Plan Supplement and Capital Accumulation Plan, subject to IRS minimum earnings requirements. Please note that “regular employees” refers to those who are not temporary staff, such as interns, and some benefits may not apply to employees in Puerto Rico.

For further details about our comprehensive benefits, we encourage you to visit the link below.

About MiniMed

MiniMed Benefits Overview

MiniMed is a full‑stack insulin delivery company dedicated to supporting people living with diabetes through every step of their journey — when and how they need it. For more than 40 years, we’ve been committed to redefining what’s possible: intelligent dosing systems designed for real life, predictive insights that stay a step ahead, and always on support when it’s needed most. At the heart of everything we do is a simple Mission: to make every day a better day for people with diabetes.

Learn more about our business, and our mission here.

It is the policy of MiniMed 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, familial status, membership or activity in a local human rights commission, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state, or local law. In addition, MiniMed will provide reasonable accommodations for qualified individuals with disabilities.

If you are applying to perform work for MiniMed 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 MiniMed reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment. MiniMed 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.