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Entry Level Medical Device Engineer Jobs (NOW HIRING)

Bachelor's degree in Electrical Engineering or a related engineering discipline. * Experience supporting medical device development or work within a highly regulated industry. * Strong understanding ...

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.

Medical Device Assembly

Wixom, MI · On-site

$16 - $17/hr

Assemble medical devices and components according to engineering drawings, work instructions, and ... Prior experience in medical device assembly, electronics assembly, or precision manufacturing ...

Medical Device Assembly

Wixom, MI · On-site

$16 - $17/hr

Assemble medical devices and components according to engineering drawings, work instructions, and ... Prior experience in medical device assembly, electronics assembly, or precision manufacturing ...

Medical Device Assembly

Wixom, MI · On-site

$16 - $17/hr

Assemble medical devices and components according to engineering drawings, work instructions, and ... Prior experience in medical device assembly, electronics assembly, or precision manufacturing ...

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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 Aug 6, 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 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 August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, and 6% Contract. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution, with an average salary of $65,130 per year, or $31.3 per hour.

Medical Device Engineer

Actalent

Aurora, CO • Hybrid

$57.69/hr

Contractor

Medical, Dental, Vision, Life, Retirement, PTO

Posted 6 days ago


Job description

Job Title: Electrical Engineer

Job Description

We're seeking an experienced Electrical Engineer to join a team focused on the development, testing, and regulatory compliance of innovative medical devices. In this role, you'll play a critical part in ensuring products meet global safety and performance standards while helping bring life-changing technologies to market.

This position offers a unique opportunity to work at the intersection of engineering, product development, quality, and regulatory compliance. You'll collaborate with cross-functional teams to support product development activities, electrical safety testing, risk management efforts, and regulatory initiatives, including compliance with EU MDR and IEC 60601 standards.


What You'll Do

As an Electrical Engineer, you will:

  • Design, evaluate, and support electrical systems used in medical devices.
  • Plan, execute, and document electrical safety testing in accordance with IEC 60601 standards.
  • Support compliance efforts related to EU Medical Device Regulation (EU MDR 2017/745).
  • Develop technical documentation required for product development and regulatory submissions.
  • Partner with Quality, Regulatory Affairs, Manufacturing, and R&D teams throughout the product lifecycle.
  • Support risk management activities in accordance with ISO 14971 methodologies.
  • Participate in design reviews, verification activities, and product investigations.
  • Work with third-party testing laboratories and certification organizations during compliance testing.
  • Analyze product issues and implement effective corrective actions.
  • Assist with audit readiness and regulatory inspections.

Required Qualifications
  • Bachelor's degree in Electrical Engineering or a related engineering discipline.
  • Experience supporting medical device development or work within a highly regulated industry.
  • Strong understanding of electrical design principles and product development processes.
  • Experience supporting or executing testing to IEC 60601 standards.
  • Knowledge of EU MDR requirements and medical device compliance activities.
  • Experience with electrical safety testing equipment and laboratory environments.
  • Familiarity with design controls, engineering documentation, and quality systems.
  • Strong analytical, troubleshooting, and problem-solving skills.
  • Excellent communication and collaboration abilities.

Preferred Experience

Candidates with any of the following will stand out:

  • IEC 60601-1-2 EMC testing experience.
  • CE Marking support for medical devices.
  • Knowledge of FDA medical device regulations.
  • Experience with ISO 13485 quality systems.
  • Experience facilitating risk management activities under ISO 14971.
  • Verification and validation testing experience.
  • Embedded systems, power electronics, or medical device software integration experience.
  • Direct interaction with Notified Bodies or third-party compliance laboratories.

Technologies & Standards

You may work with:

  • EU MDR (2017/745)
  • IEC 60601-1 Electrical Safety Standards
  • IEC 60601-1-2 EMC Standards
  • ISO 13485 Quality Systems
  • ISO 14971 Risk Management
  • Design Controls & Technical Documentation
  • Electrical Safety Testing Equipment

Why Join Us?
  • Help deliver safe and compliant medical devices that impact patient outcomes worldwide.
  • Collaborate with experienced engineering, regulatory, and quality teams.
  • Gain exposure to global regulatory requirements and advanced medical technologies.
  • Work on challenging projects involving product safety, compliance, and innovation.
  • Influence products from development through commercialization and regulatory approval.

Job Type & Location

This is a Contract position based out of Centennial, CO.

Pay and Benefits

The pay range for this position is $57.69 - $57.69/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 hybrid position in Centennial,CO.

Application Deadline

This position is anticipated to close on Aug 5, 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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