Medical Device Engineer
Listed on 2026-07-13
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Engineering
Biomedical Engineer, Quality Engineering, Test Engineer, Medical Device Industry
Medical Device Engineer
Support the development, validation, and optimization of electrochemical test methods used for next-generation medical monitoring technologies. Partner with engineers to execute validation activities, perform laboratory testing, analyze data, and generate technical documentation supporting test method development and equipment qualification efforts.
Responsibilities- Draft validation protocols and reports.
- Conduct test method validations.
- Support equipment qualification activities.
- Troubleshoot laboratory systems.
- Execute test scripts.
- Maintain calibration and qualification records.
- Analyze experimental data.
- Support engineering change control processes.
- Experience in test method validation and testing.
- R&D experience executing test methods and supporting validation activities.
- Skill in drafting validation protocols, reports, work instructions, and technical documentation.
- Ability to analyze experimental data and draw statistically supported conclusions.
- Experience in a regulated laboratory, medical device, biotech, or engineering environment.
- Strong communication skills for collaboration across engineering teams.
- Knowledge of electrochemistry, IQ, OQ, GMP, change controls, JMP, Solid Works, and equipment qualification.
Skills & Qualifications
- Bachelor's degree in Engineering, Biomedical Engineering, Chemical Engineering, Mechanical Engineering, Materials Engineering, or a related technical discipline preferred.
- Minimum 2 years of experience in laboratory testing, validation, engineering support, or medical device development.
- Experience executing and documenting test method validations.
- Technical writing experience supporting engineering or quality documentation.
- Ability to perform statistical analysis and interpret engineering test data.
- Experience with MSA/Gage R&R studies preferred.
- Experience supporting IQ/OQ activities preferred.
- Familiarity with equipment qualification, calibration, and validation documentation.
- Medical device industry experience preferred.
- Experience with electrochemical test systems is highly desirable.
- Proficiency with Excel required; JMP and Solid Works preferred.
R&D environment supporting product development and test method validation. Cross-functional collaboration with engineers, scientists, and technicians. Mix of laboratory testing, data analysis, technical writing, and validation activities. Standard business hours with hands-on laboratory work in a highly regulated medical device development setting.
Job Type & LocationThis is a Contract to Hire position based out of San Diego, CA.
Pay and BenefitsThe pay range for this position is $50.00 - $50.00/hr eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
• Medical, dental & vision
• Critical Illness, Accident, and Hospital
• 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
• Life Insurance (Voluntary Life & AD&D for the employee and dependents)
• Short and long-term disability
• Health Spending Account (HSA)
• Transportation benefits
• Employee Assistance Program
• Time Off/Leave (PTO, Vacation or Sick Leave)
This is a fully onsite position in San Diego, CA.
Final date to receive applicationsThis position is anticipated to close on Jul 24, 2026.
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