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Entry Level Medical Device Engineer Jobs (NOW HIRING)

American Hearing Care

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Medical Device Sales Representative (Base+ Commission)

Hartselle, AL · On-site

$45K - $50K/yr

Medical Device Sales Professional (HCP) American Hearing Care (AHC) is seeking a motivated ... We are open to entry-level candidates with strong communication skills and a desire to build a ...

Kelly Services

CAE Engineer - (Medical Device)

Mahwah, NJ · On-site

$45 - $55/hr

CAE Engineer - (Medical Device) * Contract Duration: 9 months - (Contract Extension possibilities) * Location : 100% ONSITE - Mahwah, NJ (07430) * Type : W2 contract (C2C OR THIRD PARTY will NOT be ...

MILLENNIUMSOFT

Medical Device Packaging Operator

Woburn, MA

$18.50 - $22.50/hr

Industrial Level Of Experience: Entry Level Employment Type: Contract on W2 (Need US Citizens or GC Holders Only) Shift hours: 6am-2:30pm Top skills: Medical device assembly and packaging operation ...

GlobalFoundries

Principal TD Device Engineer

New York, NY · On-site

$85K - $146K/yr

... engineering or device physics background and one (1) year of experience in: (1) Coding capability ... status, medical condition, mental or physical disability, national origin, race, religion ...

Globalfoundries

Principal TD Device Engineer

Malta, NY

$85K - $146K/yr

... engineering or device physics background and one (1) year of experience in: (1) Coding capability ... status, medical condition, mental or physical disability, national origin, race, religion ...

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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 Jun 5, 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?

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 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 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 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.

More about Entry Level Medical Device Engineer jobs
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:
What job categories do people searching Entry Level Medical Device Engineer jobs look for? The top searched job categories for Entry Level Medical Device Engineer jobs are:
Entry Level Medical Device Engineer jobs near you
Medical Device/Combination Product Engineer

Medical Device/Combination Product Engineer

Ventura Solutions LLC

Vernon Hills, IL • On-site, Remote

$60K - $75K/yr

Other

Medical, Dental, Vision, PTO

Posted 5 days ago

Job description

We are seeking passionate and driven Medical Device/Combination Product Engineers to join our medical device consulting team. This is an ideal opportunity for recent graduates or those with limited experience who are excited to apply their academic knowledge in real-world product development.

If you have a strong interest in medical devices, pharmaceuticals, and combination products, and are eager to gain hands-on experience in product development, design controls, and risk management, we want to meet you!

As a Medical Device/Combination Product Engineer, you will support the development and maintenance of medical devices and combination products by assisting with technical documentation, testing, and cross-functional collaboration. You’ll contribute to the creation of Design History Files (DHF), risk management files, and other engineering documentation in accordance with industry regulations and standards such as FDA 21 CFR 820 and ISO 14971.

Responsibilities

  • Assist in developing and maintaining Design History Files (DHF) and Risk Management Files for medical devices and combination products
  • Support product development activities, including gathering user needs, design inputs, and testing requirements
  • Participate in risk assessment activities, such as creating or supporting FMEAs
  • Help prepare and review technical documentation for design verification and validation
  • Research applicable regulations, standards, and guidance documents to support compliance efforts
  • Work closely with cross-functional teams, including Quality, Regulatory, Manufacturing, Human Factors, and Clinical
  • Contribute to design control activities and help ensure traceability from requirements through testing
  • Support documentation for inspections and regulatory submissions

Qualifications

  • Bachelor’s degree in Biomedical Engineering or related engineering discipline (e.g., Mechanical, Chemical, Electrical)
  • Strong academic foundation in engineering principles and a desire to apply them in a regulated industry
  • Understanding of or exposure to design control, risk management, and product development lifecycle through coursework, internships, or academic projects
  • Strong written and verbal communication skills
  • Detail-oriented with good documentation and organizational skills
  • Team-oriented with a willingness to learn and grow in a fast-paced environment

Preferred (Not Required) Experience

  • Internship, co-op, or project work related to medical devices, drug delivery, or combination products
  • Familiarity with standards like ISO 13485, ISO 14971, or FDA design control regulations
  • Exposure to tools such as FMEA, DHF documentation, or verification test planning
  • Experience with engineering software (CAD, Minitab, MATLAB, etc.)

Location

  • Northwest Chicago Suburbs or remote for the right candidate

Employee Type

  • W2 Employee

Compensation and Benefits

  • Salary: $60,000 - $75,000 annually, depending on experience
  • Choice of medical, dental, and vision plans
  • Paid Vacation Time
  • Competitive base salary

About Ventura Solutions

Ventura Solutions is a reputable end-to-end medical device and combination product consulting, staffing, and training firm. With our deep industry expertise spanning medical devices and combination products, coupled with an outstanding talent pool, we stand out as the preferred option for a diverse array of projects. On the consulting side, we integrate seamlessly into your team and manage small to complex Statement of Work (SOW) projects. On the staffing side, we help source, screen, and on-board reputable employees to fill temporary, temp to permanent, and permanent job openings. We accelerate product development, keep products compliant, and help build great organizations. For more information, visit us at www.ventura-solutions.com.

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