Reliability Engineer II

USA-MiniMed Distribution Corp. 1018

Los Angeles (CA)

On-site

USD 90,000 - 120,000

Full time

3 days ago
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Job summary

MiniMed Distribution Corp. 1018 is seeking a Reliability Engineer II to lead test strategy development for insulin therapy systems, ensuring safety and reliability in real-world use.

You will apply DOE, hypothesis testing, and capability analysis in hands-on lab work with environmental chambers, NI LabVIEW, and Instrons, collaborating with Electrical, Software R&D, Systems, and Mechanical Engineering.

Qualifications

  • Bachelor's degree in Biomedical Engineering, Mechanical Engineering, or closely related discipline with 2+ years of relevant experience.
  • Direct experience with technical documentation including engineering reports, SOPs, test protocols, and lab notebooks.
  • Familiarity with reliability and design for reliability concepts and data analysis.

Responsibilities

  • Develop test strategies and methods for insulin therapy systems and related devices.
  • Collaborate with Electrical, Software R&D, Systems, and Mechanical Engineering to improve product test methods.
  • Apply DOE, hypothesis testing, and capability analysis to support validation and reliability demonstrations.

Skills

Technical writing
LabVIEW
SolidWorks
Test methodology

Education

Biomedical Engineering
Mechanical Engineering

Tools

NI LabVIEW
SolidWorks
Environmental chambers

Job description

We anticipate the application window for this opening will close on - 30 Oct 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

At MiniMed, we build technology that millions of people living with Type 1 and Type 2 diabetes trust with their health every single day. As a Reliability Engineer II on our team, your work will be at the heart of ensuring that technology is safe, reliable, and ready for the real world.

In this hands-on and highly collaborative role, you will develop and execute test strategies and methods that put our insulin therapy systems through their paces - simulating real-world home environments to validate that our products perform flawlessly when patients need them most. From applying statistical techniques like DOE, hypothesis testing, and capability analysis to operating a broad spectrum of lab equipment including environmental chambers, signal generators, and Instrons - your technical contributions will directly influence product safety and design quality.

You will collaborate closely with Electrical Engineering, Software R&D, Systems Engineering, and Mechanical Engineering to develop robust test methods, drive root cause analysis, and contribute to risk management deliverables that protect patients. Your technical documentation - from test protocols and engineering reports to SOPs and lab notebooks - will serve as the foundation for sound engineering decisions.

If you are a curious, detail-driven engineer who thrives in a hands-on lab environment and wants their work to truly mean something - this is the role for you.

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

On Site Role in Northridge, CA
  • Develop test strategies activities associated with a family of insulin therapy systems used by individuals to effectively manage Type 1 and Type 2 diabetes.
  • Work within the broader test team to develop consistent test strategies and methods across different portions of product testing. Develop test methods to exercise products against simulated use environments, ensuring that products will continue to work safely when used in various home environments.
  • Apply statistical techniques such as hypothesis testing, DOE, regression, and capability analysis to support test method validation, design characterization, root cause analysis, and verification and reliability demonstration activities.
  • Operate a broad spectrum of lab equipment, such as environmental chambers, smart scopes, signal generators, Instrons.
  • Work with key external functions (Electrical Engineering, Software R&D, Systems Engineering, Mechanical Engineering) to develop robust test methods, root cause issues in products and test methods, and improve product design.
  • Contribute to risk management deliverables like failure modes effects analysis (dFMEA/pFMEA) and identify potential patient hazards.
Must Have: Minimum Requirements

To be considered for this role, please ensure the minimum requirements are evident on your resume

  • Bachelor's degree in Biomedical Engineering, Mechanical Engineering, or a closely related engineering discipline with 2+ years of relevant experience; or advanced degree with 0+ years of relevant experience
  • Direct experience with technical documentation including engineering reports, standard operating procedures, test protocols, and laboratory/engineering notebooks
Nice to Have:
  • Familiarity with quality system requirements, design controls, and good manufacturing practices in a regulated medical device or cGMP environment
  • Familiarity with reliability and design for reliability
  • Familiarity with root cause analysis tools (5-Why, Fishbone, Fault Tree)
  • Experience with data acquisition software such as NI LabVIEW
  • Experience with fixture design and 3D modeling tools such as SolidWorks
  • Demonstrate exceptional communication and technical writing skills while collaborating with large cross-functional teams (R&D, Ops, Regulatory, Quality).
  • Working knowledge of electromechanical devices, battery-powered devices, and/or electrochemical reactions
  • Ability to multi-task, prioritize, meets/exceed deadlines and holds themselves, and others accountable.
  • Self-starter with strong organizational skills, ability to prioritize, and a sharp focus on quality and customer experience.
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 jo

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