Principal Test Engineer

MiniMed

$121K — $205K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree with 7+ years or Master's degree with 5+ years or PhD with 3+ years of relevant experience in engineering or related field.
  • Experience with hardware and software development for test systems (LabVIEW, Python, C++).
  • Familiarity with PCBA design and fabrication (Altium Designer).
  • Strong understanding of data acquisition systems, sensors, actuators, and control systems.
  • Knowledge of FDA, ISO 13485, IEC 60601 standards and risk management.

Responsibilities

  • Lead design and development of test equipment for medical devices, ensuring standards compliance.
  • Define hardware and software requirements for testing systems.
  • Develop test methods and procedures to validate device performance and reliability.
  • Manage test equipment development projects, overseeing timelines and resource allocation.
  • Collaborate with teams to align testing strategies with product development goals.
  • Oversee validation activities in compliance with regulatory standards.
  • Deploy test equipment and provide technician training for effective operations.

Benefits

  • Comprehensive health, dental, and vision insurance coverage.
  • Access to Health Savings and Flexible Spending Accounts.
  • 401(k) plan with company match and employee stock purchase plan.
  • Robust paid time off policy and holiday pay.
  • Short-term and long-term disability coverage and life insurance.
Full Job Description
We anticipate the application window for this opening will close on - 16 Jun 2026

About the Role

We are seeking a highly skilled and experienced Principal Test Engineer to join our team in the medical device industry. In this role, you will lead the design, development, and deployment of complex test equipment to ensure the highest quality and reliability of our innovative medical devices. You will collaborate with cross-functional teams, including R&D, manufacturing, and quality assurance, to deliver robust testing solutions that meet regulatory and industry standards. This role requires a strong technical background, leadership skills, and a passion for advancing healthcare technologies.

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

Test Equipment Design & Development:
  • Lead the design and development of complex automated and manual test equipment for medical devices, ensuring compliance with industry standards and internal requirements.
  • Define system architecture, hardware, and software requirements for test equipment.
  • Develop test methods, protocols, and procedures to validate product functionality, performance, and reliability.


Project Management:
  • Manage multiple test equipment development projects from concept to deployment, including timelines, budgets, and resource allocation.
  • Collaborate with cross-functional teams to align testing strategies with product development goals and manufacturing processes.

Validation and Verification:
  • Oversee the validation and verification of test equipment, including IQ, OQ, and PQ activities, in compliance with FDA, ISO, and other regulatory standards.
  • Ensure all test equipment meets safety and quality requirements before deployment.


Deployment and Support:
  • Lead the deployment of test equipment to manufacturing facilities and provide training to operators and technicians.
  • Troubleshoot and resolve technical issues with test equipment in a timely manner.


Continuous Improvement:
  • Identify opportunities for process improvements, cost reductions, and increased efficiency in test equipment design and deployment.
  • Stay up-to-date with emerging technologies and industry trends to drive innovation in test methodologies.


Documentation and Compliance:
  • Develop and maintain detailed documentation, including design specifications, test plans, and validation reports.
  • Ensure compliance with all applicable regulatory standards, such as FDA, ISO 13485, and IEC 60601.


Mentorship and Leadership:
  • Mentor and guide junior engineers and technicians, fostering a culture of technical excellence and continuous learning.
  • Act as a technical expert and provide guidance on complex engineering challenges


Minimum Qualifications:

Requires a bachelor's degree and minimum of 7 years of relevant experience OR Master's degree with a minimum of 5 years relevant experience OR PhD with 3 years relevant experience.

Preferred Qualifications:
  • Proficiency in hardware and software development for test systems (LabVIEW, Python, C++, or similar).
  • Proficiency in PCBA Design and Fabrication (Altium Designer)
  • Strong knowledge of data acquisition systems, sensors, actuators, and control systems.
  • Experience with automated test equipment (ATE) and robotics is a plus.
  • Regulatory Knowledge:
  • Familiarity with FDA, ISO 13485, IEC 60601, and other relevant medical device standards.
  • Experience with risk management and Design for Testability (DFT) principles.
  • Soft Skills:
  • Strong problem-solving, analytical, and critical-thinking skills.
  • Excellent communication and interpersonal skills to work effectively with cross-functional teams.


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

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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