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Volunteer 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 ...

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 ...

Evapco

Product Development Engineer

Taneytown, MD · On-site

$72K - $90K/yr

Product Development Engineer Regular Full Time Taneytown, MD, US Job Overview: The Product ... Profit Sharing Bonus - which is paid twice per year * (k)larity Plan - Voluntary Employee ...

Evapco

Product Development Engineer

Taneytown, MD · On-site

$72K - $90K/yr

Product Development Engineer Regular Full Time Taneytown, MD, US Job Overview: The Product ... Profit Sharing Bonus - which is paid twice per year * (k)larity Plan - Voluntary Employee ...

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All JobsVolunteer Biomedical Product Development Engineer Jobs

Volunteer Biomedical Product Development Engineer information

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$39.5K

$87.9K

$132.5K

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

As of Jul 14, 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:
Volunteer Biomedical Product Development Engineer jobs near you
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.