Principal R-D Engineer

MiniMed

• $121K — $205K *
Healthcare
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's or Master's in Biomedical Engineering, Chemical Engineering, or related field
  • 7+ years (Bachelor's) or 5+ years (Master's) of professional experience
  • Experience in the medical device industry is a plus
  • Familiarity with mechanical and/or electrochemical systems
  • Knowledge of in-vitro and in-vivo testing of medical devices

Responsibilities

  • Lead development and implementation of problem-solving tools and methodologies
  • Proactively identify and resolve complex issues
  • Troubleshoot and determine root causes of failures in biosensors
  • Develop test methods for feasibility and qualification of processes
  • Document protocols and reports throughout product development
  • Design and enhance test methods and measurement techniques
  • Develop verification and validation strategies for product testing

Benefits

  • Comprehensive health, dental, and vision insurance
  • 401(k) plan with company match
  • Short-term and long-term disability coverage
  • Paid time off and holidays
  • Employee Stock Purchase Plan
  • Access to Employee Assistance Program
  • Flexible benefits package tailored to employee needs
Full Job Description
We anticipate the application window for this opening will close on - 30 Nov 2026

About the Role

MiniMed is looking for a Principal R-D Engineer to join our office Northridge CA. This role is onsite 5 days per week.

This role is within Medtronic Diabetes - Continuous Glucose Monitoring (CGM) Sensor R&D team. In this role, you will be responsible for leading improvement efforts in the development of next generation CGM products and sustaining R&D. There will be strong emphasis on utilizing Design for Reliability and Manufacturability (DRM) principles and problem-solving methodologies (DMAIC). You will be responsible for leading the Failure Analysis efforts throughout different phases of sensor product development.

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.

Responsibilities may include the following and other duties may be assigned:
  • Lead the development and implementation of tools and methodologies for effective problem-solving, failure analysis and root cause investigation.
  • Proactively identify issues, achieve resolution, and resolve problems of significant complexity.
  • Troubleshooting and identifying the root cause of failures in complex microfabricated electrochemical biosensors.
  • Develop test methods and strategies to support early feasibility, characterization, and qualification of processes.
  • Document protocols and reports at various stages of product development.
  • Design and develop advanced new test methods, improve existing test methods, measurement techniques, and fixtures.
  • Develop verification and validation test strategies and equipment to enable the execution of product testing and perform analysis to evaluate designs for short and long-term performance and reliability.
  • Present information to cross functional audiences and management.
  • Conduct hands-on lab work, define failure analysis strategy, and recommend corrective actions/fixes to failures at different phases of product development.
  • Ensure designs meet and exceed product specifications, regulatory requirements, national and international standards.
  • Lead product improvement efforts through CAPAs.


TECHNICAL SPECIALIST CAREER STREAM:
  • An individual contributor with responsibility in our technical functions to advance existing technology or introduce new technology and therapies.
  • Formulates, delivers and/or manages projects assigned and works with other stakeholders to achieve desired results. May act as a mentor to colleagues or may direct the work of other lower level professionals.
  • The majority of time is spent delivering R&D, systems or initiatives related to new technologies or therapies - from design to implementation - while adhering to policies, using specialized knowledge and skills.


DIFFERENTIATING FACTORS

Autonomy:
  • Recognized expert, managing large projects or processes.
    Exercises considerable latitude in determining deliverables of assignments, with limited oversight from manager.
  • Coaches, reviews and delegates work to lower level specialists.


Organizational Impact:
  • Contributes to defining the direction for new products, processes, standards, or operational plans based on business strategy with a significant impact on work group results.
  • May manage large projects or processes that span outside of immediate job area.


Innovation and Complexity:
  • Problems and issues faced are difficult, moderately complex and undefined, and require detailed information gathering, analysis and investigation.
  • Develops solutions to moderately complex problems, and/or makes moderate to significant improvements of processes, systems or products independently to enhance performance of job area.
    Implements solutions to problems.


Communication and Influence:
  • Represents organization as a primary contact for specific projects and initiatives; communicates with internal and external customers and vendors at various levels.
  • May negotiate with others to reach understanding or agreement, and influence decision-making.


Leadership and Talent Management:
  • Typically provides guidance, coaching and training to other employees within job area.
  • Typically manages major / moderately complex projects, involving delegation of work and review of work products, at times acting as a team leader.


Must Have: Minimum Requirements

To be considered for this role, please ensure the minimum requirements are evident on your resume.
  • Bachelors of Science in Biomedical Engineering, Chemical Engineering or related Engineering field with 7+ years of professional experience or Masters of Science in Biomedical Engineering, Chemical Engineering, or related Engineering field with 5+ years of professional experience;

#BetterDaysStartNow

Nice to Have
  • 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):$109,000.00 - $185,000.00
For roles located in California, Seattle WA, Washington DC, Boston MA, and New York City, the salary range is $121,000.00 - $205,000.00 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.

MiniMed Benefits Overview

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