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Entry Level Medical Device Engineer Jobs in Raleigh, NC

Varsity Tutors

Biomedical Engineering Tutor

Raleigh, NC · Remote

$18 - $40/hr

Ability to explain signal processing for biosignals, finite element analysis, drug delivery systems, and medical device design principles while preparing students for biomedical engineering ...

Varsity Tutors

Biomedical Engineering Tutor

Durham, NC · Remote

$18 - $40/hr

Ability to explain signal processing for biosignals, finite element analysis, drug delivery systems, and medical device design principles while preparing students for biomedical engineering ...

Intellectt INC

R&D lab Technician

Durham, NC · On-site

Associate's or Bachelor's degree in Biology, Chemistry, Biomedical Engineering, Material Science, or a related scientific field. * 1-3 years of laboratory or R&D experience (medical device ...

New

DivIHN Integration Inc

Quality Engineer I

Durham, NC · On-site

$69K - $89K/yr

Minimum of 2 years of manufacturing quality engineering experience (preferably in a regulated industry such as health care, medical device, pharmaceutical, etc). Desired Experience/Qualifications:

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Entry Level Medical Device Engineer information

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

As of Jul 15, 2026, the average hourly pay for entry level medical device engineer in Raleigh, NC is $30.44, according to ZipRecruiter salary data. Most workers in this role earn between $26.63 and $33.65 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.
More about Entry Level Medical Device Engineer jobs
What are the most commonly searched types of Medical Device Engineer jobs in Raleigh, NC? The most popular types of Medical Device Engineer jobs in Raleigh, NC are:
What are popular job titles related to Entry Level Medical Device Engineer jobs in Raleigh, NC? For Entry Level Medical Device Engineer jobs in Raleigh, NC, the most frequently searched job titles are:
What job categories do people searching Entry Level Medical Device Engineer jobs in Raleigh, NC look for? The top searched job categories for Entry Level Medical Device Engineer jobs in Raleigh, NC are:
What cities near Raleigh, NC are hiring for Entry Level Medical Device Engineer jobs? Cities near Raleigh, NC with the most Entry Level Medical Device Engineer job openings:
Entry Level Medical Device Engineer jobs near you
Infographic showing various Entry Level Medical Device Engineer job openings in Raleigh, NC as of July 2026, with employment types broken down into 72% Full Time, 20% Part Time, 1% Temporary, and 7% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $63,311 per year, or $30.4 per hour.

Senior Regulatory Affairs Specialist

Osv_bioventus

Durham, NC • Hybrid

Full-time

Re-posted 5 days ago

Job description

Are you ready to work for a more active world?

At Bioventus, our business depends on developing our people. We invest in you and challenge you to be the best. We value our colleagues for their different perspectives and individual contributions, and our leaders listen. Our success rests on working together to achieve shared goals and rewards. Join a diverse team of global colleagues driven to help patients resume and enjoy active lives.

Bioventus LLC., seeks Senior Regulatory Affairs Specialist (Durham, NC).

Duties:

  • Author and submit applications 510(k), PMA Supplements and, Technical Documentation to receive product clearance / approvals for new products and maintain existing registrations globally.
  • Author and maintain Technical Files compliant to the MDD 93/42/EEC and Technical Documentation compliant to the EU MDR 2017/745.
  • Communicate with Regulatory Agencies regarding submissions, and changes of products, including manufacturing, design and new product development.
  • Serve as Subject Matter Expert to represent Regulatory during internal audits and external audits by regulatory agencies.
  • Review protocols and reports for scientific validity and compliance to regulatory standards and provide scientific judgement to guide cross functional teams.
  • Perform Regulatory Assessments for design, manufacturing, and labeling changes to ensure compliance with regulations and standards where the product is registered.
  • Research requirements and set priorities while maintaining project schedules. Provide guidance and oversight to team members related to regulatory compliance.
  • Review marketing literature for compliance with applicable regulations and company policies and procedures.

Required: Master's degree or foreign equivalent in Regulatory Affairs, Pharmaceutical Sciences or related field plus 3 years of experience in the job offered, as Regulatory Engineer or related regulatory affairs position within the medical and/or diagnostic device industry.

Must have 3 years of experience with:

  • Regulatory assessment of engineering/design change execution.
  • Working with or providing guidance to cross-functional or offshore team in preparation of documents for regulatory agency submissions.
  • Regulatory registrations in at least 3 or more of the following agencies or regions (FDA, EMEA, Canada, LATAM, Japan, Australia).
  • Project management.
  • Preparing and reviewing documentation regarding submissions and product changes of medical devices.

Must have experience working with medical device registrations compliant with Medical Device Regulation and EU Medical Device Directive.

Hybrid role model position, working 3 days in office and 2 days from within normal commuting distance of the office location.

National travel required 25% of the time.

Are you the top talent we are looking for?

Apply now! Hit the "Apply" button to send us your resume and cover letter.

Bioventus is committed to fostering an inclusive and diverse community of employees with a strong sense of belonging. We believe we are bettered by all forms ofdiversity andtake pride in working with top talent from every walk of life. In the spirit of inclusivity, qualified applicants will be considered without regard to age, ethnicity, disability, gender, veteran status, gender expression, gender identity, nationality, race, religion or sexual orientation.All individuals, regardless of personal characteristics, are encouraged to apply.

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