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Internship Biomedical Product Development Engineer Jobs

Polyzen, LLC

Product Development Engineer

Apex, NC · On-site

Bachelor's degree in chemical engineering, mechanical engineering, biomedical engineering, or ... product development environment * Ability to learn manufacturing process development ...

Polyzen LLC

Product Development Engineer

Apex, NC · On-site

Bachelor's degree in chemical engineering, mechanical engineering, biomedical engineering, or ... product development environment * Ability to learn manufacturing process development ...

Solesis

Product Development Engineer

Apex, NC · On-site

Bachelor's degree in chemical engineering, mechanical engineering, biomedical engineering, or ... product development environment * Ability to learn manufacturing process development ...

First Quality

Product Development Engineer

Macon, GA · On-site

We are seeking a Product Development Engineer for our First Quality Baby Products facility located ... Chemical, Biomedical, or Mechanical Engineering) or equivalent; additional business studies ...

Merck Group

Product Development Engineer III

Bedford, MA · On-site

$84K - $127K/yr

We are seeking a Product Development Engineer to work within MilliporeSigma Process Solutions ... Bachelor's degree in Mechanical Engineering, Chemical Engineering, Biomedical Engineering, Material ...

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Internship Biomedical Product Development Engineer information

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How much do internship biomedical product development engineer jobs pay per hour?

As of Jul 14, 2026, the average hourly pay for internship biomedical product development engineer in the United States is $21.19, according to ZipRecruiter salary data. Most workers in this role earn between $17.31 and $24.04 per hour, depending on experience, location, and employer.

What types of projects and responsibilities can I expect as an Internship Biomedical Product Development Engineer?

As an Internship Biomedical Product Development Engineer, you will typically support product design and prototyping, conduct laboratory testing, and assist with documentation for regulatory compliance. You'll often collaborate closely with cross-functional teams, including engineers, quality assurance, and clinical specialists, to bring innovative medical devices or products from concept to early development stages. Common challenges include balancing creative problem-solving with strict regulatory requirements and managing multiple tasks to meet project deadlines. This role offers hands-on experience that can lead to full-time opportunities and valuable exposure to the entire product development lifecycle.

What is the difference between Internship Biomedical Product Development Engineer vs Biomedical Research Assistant?

AspectInternship Biomedical Product Development EngineerBiomedical Research Assistant
Required CredentialsEnrolled in or recent graduate of biomedical engineering, bioengineering, or related fieldsTypically pursuing or holding a degree in biology, biomedical sciences, or related areas
Work EnvironmentProduct development labs, engineering teams, R&D departmentsResearch labs, academic institutions, clinical research settings
Employer & Industry UsageMedical device companies, biotech firms, healthcare product developersUniversities, research institutes, hospitals

While both roles involve biomedical sciences, the Internship Biomedical Product Development Engineer focuses on designing and developing medical devices and products, often in a corporate setting. In contrast, a Biomedical Research Assistant primarily conducts scientific research, experiments, and data analysis in academic or clinical research environments. The former emphasizes engineering and product innovation, whereas the latter centers on scientific investigation and data collection.

What does an Internship Biomedical Product Development Engineer do?

An Internship Biomedical Product Development Engineer assists in designing, developing, and testing medical devices and healthcare products under the supervision of experienced engineers. Interns may participate in research, prototyping, data analysis, and documentation to support product development from concept to prototype. They often collaborate with cross-functional teams, learn industry regulations, and gain hands-on experience with tools and technologies used in biomedical engineering. This role offers valuable exposure to real-world challenges in healthcare innovation and product design.

What are the key skills and qualifications needed to thrive as an Internship Biomedical Product Development Engineer, and why are they important?

To thrive as an Internship Biomedical Product Development Engineer, you need a strong background in biomedical engineering principles, problem-solving, and familiarity with product development processes, typically gained through coursework or related internships. Experience with CAD software, lab equipment, and knowledge of regulatory standards such as FDA or ISO is highly valuable. Strong teamwork, communication skills, and a detail-oriented mindset help interns collaborate effectively and contribute to innovative solutions. These competencies are essential to ensure the safe, effective, and compliant development of biomedical products within multidisciplinary teams.
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Internship Biomedical Product Development Engineer jobs near you
Infographic showing various Internship Biomedical Product Development Engineer job openings in the United States as of July 2026, with employment types broken down into 2% Internship, 1% As Needed, 83% Full Time, 13% Part Time, and 1% Contract. Highlights an 86% Physical, 4% Hybrid, and 10% Remote job distribution, with an average salary of $44,083 per year, or $21.2 per hour.
Product Development Engineer

Product Development Engineer

Sterling Engineering Inc.

North Chicago, IL • On-site

$50 - $56/hr

Contractor

Medical, Dental, Vision, Retirement, PTO

Posted 4 days ago

New

Job description

Job Title: Product Development Engineer (Medical Device)
Location: North Chicago, IL
Hire Type: 12 month contract
Target Pay Rate: $50-$56/hr
Benefits: PTO, paid holidays, BCBS medical plans, dental/vision plans, 401(k), ESOP

Must-Have Skills:
  • Bachelor's degree in Mechanical, Biomedical, Bioengineering, Chemical Engineering, or related engineering discipline
  • 3+ years of medical device, combination product, or pharmaceutical product development experience
  • Experience with Design History Files (DHF) and design controls
  • Experience supporting commercialized/on-market products
  • Strong technical writing, data analysis, and problem-solving skills
  • Experience working with cross-functional teams in a regulated environment
Job Summary:

The Product Development Engineer supports commercially released medical devices and combination products through product lifecycle management, engineering change implementation, supplier change assessments, and manufacturing support. This role partners with cross-functional teams to evaluate, document, test, and implement product changes while ensuring compliance with quality and regulatory requirements.

Job Duties:
  • Support product lifecycle management activities for commercialized medical devices and combination products
  • Evaluate supplier, material, and manufacturing changes to determine product impact
  • Maintain Design History File (DHF) documentation and ensure design traceability
  • Develop and execute verification testing protocols for product and process changes
  • Analyze engineering and test data, investigate deviations, and prepare technical reports
  • Support risk management activities and regulatory compliance initiatives
  • Collaborate with Engineering, Quality, Regulatory, Manufacturing, Supply Chain, and external suppliers to implement product changes
  • Drive continuous improvement initiatives related to engineering processes and documentation
  • Provide technical support for manufacturing and ongoing product performance
Qualifications:
  • Bachelor's degree in Mechanical Engineering, Biomedical Engineering, Bioengineering, Chemical Engineering, or a related technical discipline
  • 3+ years of experience developing or supporting medical devices, combination products, or other regulated products
  • Experience with Design History Files (DHF), design controls, and engineering documentation
  • Knowledge of FDA regulations and medical device quality systems preferred
  • Familiarity with ISO 13485, ISO 14971, ISO 10993, MDR, or similar regulatory standards is a plus
  • Experience with supplier change management is preferred
  • Strong communication, analytical, and problem-solving skills
  • Ability to work independently and collaborate effectively with cross-functional teams
Qualified applicants will receive consideration for employment without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or genetic information.