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Entry Level Medical Device Engineer Jobs (NOW HIRING)

Medical Device Engineer Support the development, validation, and optimization of electrochemical test methods used for next-generation medical monitoring technologies. Partner with engineers to ...

Job Title: Medical Device Assembler Location: Madison, WI (Onsite) Pay Rate: $23-24/hr on W2 ... Engineering group as required. Working Conditions: Clean, temperature controlled environment.

**Job Title: **Med-Device Assembler (x2) **Pay Rate: **$21-$23/hr. ($21/hr. without soldering $23/hr ... Collaborate with Manufacturing Engineering to support lean manufacturing processes **Qualifications:

Medical Device Assembler

Carlsbad, CA

$18.50 - $22.50/hr

Medical Device Manufacturing Technician This role focuses on the manufacturing and assembly of ... Collaborate with engineers to develop and refine process documentation for manufacturing and ...

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Entry Level Medical Device Engineer information

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$14

$31

$50

How much do entry level medical device engineer jobs pay per hour?

As of Jul 16, 2026, the average hourly pay for entry level medical device engineer in the United States is $31.31, according to ZipRecruiter salary data. Most workers in this role earn between $27.40 and $34.62 per hour, depending on experience, location, and employer.

What does an entry level medical device engineer do?

An entry level medical device engineer assists in designing, developing, and testing medical devices such as implants, diagnostic equipment, or surgical tools. They often work as part of a team under the supervision of experienced engineers, ensuring products meet regulatory standards and function safely and effectively. Responsibilities may also include documenting results, conducting research, and supporting manufacturing or quality assurance processes. This role provides hands-on experience with engineering principles in the healthcare industry and often serves as a starting point for more specialized or senior positions.

What is the difference between Entry Level Medical Device Engineer vs Quality Assurance Technician?

AspectEntry Level Medical Device EngineerQuality Assurance Technician
Required CredentialsBachelor's in engineering, biomedical or related fieldBachelor's in science, engineering, or related field; certifications optional
Work EnvironmentDesign labs, manufacturing facilities, R&D teamsManufacturing plants, quality control labs
Employer & Industry UsageMedical device companies, biotech firmsManufacturers, healthcare device companies

Entry Level Medical Device Engineers focus on designing and developing medical devices, while Quality Assurance Technicians ensure products meet quality standards. Both roles are essential in the medical device industry and often work closely to ensure product safety and compliance.

What Does an Entry-Level Medical Device Engineer Do?

As an entry-level medical device engineer, your duties include the research, design, and development of medical devices and healthcare products and equipment. An entry-level engineer works as part of a research and development team. You typically have specific tasks such as performing research on materials or testing a device in a laboratory setting or during a clinical trial. In addition to responsibilities related to design and development, entry-level engineers often document tests and trials, collect and organize data, and create drawings and plans using computer-aided design software.

What types of projects and responsibilities can an entry level medical device engineer expect during their first year on the job?

As an entry level medical device engineer, you can expect to work closely with cross-functional teams—including design, quality, and manufacturing—to support product development and improvements. Your responsibilities may include assisting in prototyping, conducting testing and data analysis, and maintaining detailed documentation to ensure regulatory compliance. You’ll likely gain hands-on experience troubleshooting devices, collaborating in design reviews, and participating in validation activities. This role provides an excellent foundation for learning industry standards and building technical and teamwork skills essential for career advancement.

What are the key skills and qualifications needed to thrive as an Entry Level Medical Device Engineer, and why are they important?

To thrive as an Entry Level Medical Device Engineer, you need a bachelor's degree in biomedical, mechanical, or electrical engineering, along with a solid understanding of engineering principles and medical device regulations. Familiarity with CAD software, prototyping tools, and knowledge of FDA or ISO standards is typically required. Strong problem-solving skills, attention to detail, and effective teamwork and communication abilities help you stand out in this role. These competencies are critical for ensuring the safe design and development of innovative medical devices that meet regulatory standards and patient needs.
What cities are hiring for Entry Level Medical Device Engineer jobs? Cities with the most Entry Level Medical Device Engineer job openings:
What are the most commonly searched types of Medical Device Engineer jobs? The most popular types of Medical Device Engineer jobs are:
What states have the most Entry Level Medical Device Engineer jobs? States with the most job openings for Entry Level Medical Device Engineer jobs include:
Infographic showing various Entry Level Medical Device Engineer job openings in the United States as of July 2026, with employment types broken down into 75% Full Time, 18% Part Time, and 7% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $65,130 per year, or $31.3 per hour.
Medical Device Engineer

Medical Device Engineer

Actalent

San Diego, CA

$50/hr

Contractor

Medical, Dental, Vision, Life, Retirement, PTO

Posted 6 days ago


Job description

Job Title: Medical Device Engineer

Job Description

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.

Essential Skills

  • 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, SolidWorks, and equipment qualification.

Additional 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 SolidWorks preferred.

Work Environment

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 & Location

This is a Contract to Hire position based out of San Diego, CA.

Pay and Benefits

The 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)

Workplace Type

This is a fully onsite position in San Diego,CA.

Application Deadline

This position is anticipated to close on Jul 24, 2026.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.


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About Actalent

Sourced by ZipRecruiter

Actalent connects passion with purpose. Our scalable talent solutions and services capabilities drive value and results and provide the expertise to help our customers achieve more. Every day, our experts around the globe are making an impact. We're supporting critical initiatives in engineering and sciences that advance how companies serve the world. Actalent promotes consultant care and engagement through experiences that enable continuous development. Our people are the difference. Actalent is an operating company of Allegis Group, the global leader in talent solutions.

Company size

5,001 - 10,000 Employees

Headquarters location

Hanover, MD, US

Year founded

1983

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