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Internship Biomedical Product Development Engineer Jobs

Coloplast

Product Development Engineer

Minneapolis, MN · On-site

$90K - $120K/yr

Bachelor's degree in Biomedical, Mechanical or Chemical Engineering or equivalent * 3+ years of full-time experience in a product development role within the medical device industry * Experience ...

Swoon Staffing

Product Owner Intern

Grand Rapids, MI · On-site

$16/hr

... development What We're Looking For * Currently pursuing a degree (CS, Engineering, Biomedical ... Strong communication & detail-oriented Why This Internship? * Ideal for candidates exploring a ...

Merck Group

Product Development Engineer III

Bedford, MA · On-site

$84.90K - $127.30K/yr

LS-PS-RDFA Aseptic Product Development Recruiter: Beverly Dellisola This information is for ... Bachelor's degree in Mechanical Engineering, Chemical Engineering, Biomedical Engineering, Material ...

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 ...

Jj

Product Development Engineer

West Chester, PA · On-site

Biomedical Engineering Job Category: Scientific/Technology All Job Posting Locations: West Chester ... internship or research. * Experience with machining of metals or exposure to a machine shop ...

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

As of May 30, 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 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.

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 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 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.

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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 May 2026, with employment types broken down into 1% Internship, and 99% Full Time. Highlights an 81% Physical, and 19% Remote job distribution, with an average salary of $44,083 per year, or $21.2 per hour.
Product Development Engineer

Product Development Engineer

Intellectt INC

Minnetonka, MN • On-site

Contractor

Posted 8 days ago

Job description

Job title: Product Development Engineer
Location: Minnetonka, MN
Duration: 12 Months
 
Job Summary

The Product Development Engineer supports new product development and commercialization by executing engineering tasks, testing, documentation, data analysis, equipment qualification, and design control activities in a regulated medical/pharmaceutical environment.

Key Responsibilities

  • Support new product development using engineering fundamentals.
  • Install, qualify, and support R&D equipment.
  • Perform engineering testing, data analysis, and technical report writing.
  • Develop and validate test methods for materials and inspections.
  • Maintain Design History Files (DHF) and support DFMEA/risk management.
  • Prepare DMR documentation such as specifications, test methods, and manufacturing instructions.
  • Participate in design reviews, root cause analysis, and failure investigations.
  • Support technology transfer and process validation for new product launch.
  • Ensure compliance with FDA regulations, and safety procedures.

Required Skills

  • BS in Engineering; Mechanical or Biomedical preferred.
  • Good understanding of design control and quality systems.
  • Knowledge of statistics: Gage R&R, capability analysis, DoE, normality, acceptance sampling.
  • Experience with technical writing and data analysis.
  • Familiarity with FDA-regulated environments: 21 CFR 211, 21 CFR 820, ISO 13485.
  • Knowledge of root cause analysis tools like 5 Whys and Ishikawa.
  • Proficiency in Excel/Minitab.

For more information, please reach out at 732-719-4936 or share your updated resume with padma.priya@intellectt.com.