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Volunteer Biomedical Product Development Engineer Jobs

Product Development Engineer

Minneapolis, MN ยท 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 ...

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

Product Development Engineer III

Bedford, MA ยท 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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Volunteer Biomedical Product Development Engineer information

See salary details

$39.5K

$87.9K

$132.5K

How much do volunteer biomedical product development engineer jobs pay per year?

As of Jun 12, 2026, the average yearly pay for volunteer biomedical product development engineer in the United States is $87,884.00, according to ZipRecruiter salary data. Most workers in this role earn between $72,000.00 and $100,000.00 per year, depending on experience, location, and employer.

What is the difference between Volunteer Biomedical Product Development Engineer vs Biomedical Research Associate?

AspectVolunteer Biomedical Product Development EngineerBiomedical Research Associate
CredentialsRelevant degrees, certifications optional; volunteer statusTypically requires a bachelor's or master's in biomedical sciences
Work EnvironmentProduct development labs, hospitals, nonprofit organizationsResearch labs, academic institutions, hospitals
Employer & IndustryMedical device companies, nonprofits, startupsUniversities, research institutes, biotech firms

The Volunteer Biomedical Product Development Engineer focuses on designing and improving medical devices or products, often in a volunteer capacity, while the Biomedical Research Associate conducts scientific research to understand biological processes. Both roles require relevant knowledge but differ in their primary focus and work environment.

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

To thrive as a Volunteer Biomedical Product Development Engineer, you need a solid background in biomedical engineering, product design, and problem-solving, usually supported by a relevant degree or coursework. Familiarity with CAD software, prototyping tools, and regulatory standards such as FDA or ISO is typically required. Strong teamwork, resourcefulness, and effective communication skills help you collaborate with diverse teams and stakeholders. These skills and qualities are crucial for developing safe, innovative medical products that address real healthcare needs, often with limited resources.

What types of projects and collaboration opportunities can a Volunteer Biomedical Product Development Engineer expect to work on?

As a Volunteer Biomedical Product Development Engineer, you will typically engage in projects that focus on designing, prototyping, or improving medical devices intended for underserved communities or non-profit initiatives. Collaboration is a key part of the role; you'll work closely with multidisciplinary teams that may include clinicians, regulatory experts, and other engineers. Expect to contribute to brainstorming sessions, conduct user needs assessments, and help with documentation for regulatory compliance. This environment provides valuable exposure to end-to-end product development and offers opportunities for professional growth through hands-on experience and mentorship.

What does a Volunteer Biomedical Product Development Engineer do?

A Volunteer Biomedical Product Development Engineer contributes their expertise to develop and improve medical devices and health-related products, often for non-profit organizations or underserved communities. Their work involves designing, prototyping, testing, and refining biomedical products to ensure safety, effectiveness, and compliance with regulatory standards. Volunteers in this role may also collaborate with multidisciplinary teams, assist with documentation, and support clinical trials, all while working without monetary compensation to help advance healthcare solutions.
What cities are hiring for Volunteer Biomedical Product Development Engineer jobs? Cities with the most Volunteer Biomedical Product Development Engineer job openings:
What are the most commonly searched types of Biomedical Product Development Engineer jobs? The most popular types of Biomedical Product Development Engineer jobs are:
What states have the most Volunteer Biomedical Product Development Engineer jobs? States with the most job openings for Volunteer Biomedical Product Development Engineer jobs include:
Product Development Engineer

Product Development Engineer

Intellectt INC

Minnetonka, MN โ€ข On-site

Contractor

Posted 20 days ago


Job description

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