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Volunteer Biomedical Product Development Engineer Jobs

Primary Function of Position The Product Development Engineer will lead design and development ... Minimum Bachelors Degree in Mechanical or Biomedical Engineering or equivalent. Working Conditions ...

Primary Function of Position The Product Development Engineer will lead design and development ... Minimum Bachelors Degree in Mechanical or Biomedical Engineering or equivalent. Working Conditions ...

Bachelor of Science in Industrial Design, Mechanical Engineering, Biomedical Engineering, Product Design, or related technical discipline. * 3+ years of product development, design engineering, or R& ...

Product Development Engineer

Scranton, PA ยท On-site

$70K - $120K/yr

Product Development Engineer Reports To: New Product Development Manager Department: Engineering ... Voluntary Life Insurance About PLASKOLITE PLASKOLITE is a global leader in manufacturing of ...

Product Development Engineer

Taneytown, MD ยท 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 ...

Product Development Engineer

Thousand Oaks, CA ยท On-site

$98K - $120K/yr

Bachelor's degree in Mechanical Engineering or Biomedical Engineering * Minimum 2 years' experience in product development; medical device or another highly regulated industry is highly preferred

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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 Aug 23, 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 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 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 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 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 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:

Sr. Product Development Engineer

Enerpac Tool Group Corp

Cortland, NY โ€ข On-site

$96K - $144K/yr

Full-time

Re-posted 2 days ago


Job description

Overview
CORTLAND - Who we are?
Cortland Biomedical is wholly owned by Enerpac Tool Group. Enerpac Tool Group Corp. is a premier industrial tools, services, technology, and solutions provider serving a broad and diverse set of customers and end markets for mission-critical applications in more than 100 countries. The Company makes complex, often hazardous jobs possible safely and efficiently. Enerpac Tool Group's businesses are global leaders in high pressure hydraulic tools, controlled force products, and solutions for precise positioning of heavy loads that help customers safely and reliably tackle some of the most challenging jobs around the world. The Company was founded in 1910 and is headquartered in Milwaukee, Wisconsin. Enerpac Tool Group common stock trades on the NYSE under the symbol EPAC.
Enerpac Tool Group Corp. is a premier industrial tools, services, technology, and solutions provider serving a broad Cortland Biomedical custom builds high-performance biomedical textile structures. The company applies over 40 years of experience in textile engineering and advanced fabric design methods to braid, knit and woven products that meet the demands of a diverse set of customers in the biomedical product space. The company also offers a full range of design, development and manufacturing services as well as a wide variety of biomedical materials. Never comfortable with the status quo, complex biomedical textile challenges are tackled with agility, credibility and curiosity.
For further information on Cortland Biomedical, visit the Company's website at https://www.cortlandbiomedical.com
For further information on Enerpac Tool Group and its businesses, visit the Company's website at https://www.enerpactoolgroup.com
Summary - basic function of the role
Reports into the Sales & New Business Development (NBD) organization. Leads the management of the design and development of biomedical textile products, manufacturing methods, and test methods with a focus on design feasibility, customer communication, design control documentation, and project timelines, to ensure products meet and exceed customer expectations.
Work Schedule: Monday - Friday; evenings and weekends may be required
Location: In-office Monday - Friday
850 Lime Hollow Rd.
Cortland, NY13045
Salary Range: $96,500 - $144,750
Anticipated Hire Date: September 2026
This role is not eligible for sponsorship now or in the future.
Job Duties and Responsibilities
  • Consult and guide customers to biomedical textile solutions by leveraging textile forming techniques such as braiding, knitting, weaving, as well as post-processing methods to create novel structures.
  • Collaborate with Sales & Sales Engineering to gather voice of customer, evaluate new project opportunities, and make strategic project decisions.
  • Represent Cortland Biomedical as biomedical textile design expert.
  • Establish design and manufacturing feasibility of new products.
  • Document engineering work in protocols and reports. Establish documentation best practices and mentor junior engineers.
  • Own execution of engineering changes and CAPAs. Establish best practices and mentor junior engineers.
  • Create and maintain design control documentation including traceability matrix, design and development plan, and other quality management system (QMS) documentation in compliance with Cortland Biomedical QMS standards. Provide continuous improvement ideas and solutions for design and development documentation.
  • Drive the progression of development projects through the Cortland Biomedical design and development phase gate process through execution and documentation of timely cross-functional design reviews in compliance with Cortland Biomedical QMS standards. Provide continuous improvement ideas and solutions for design and development processes and systems.
  • Collaborate with engineering, operations, and quality to ensure all QMS documentation is completed in a timely manner, consistent with the project timeline.
  • Manage the details of development projects including resources, timelines/Gantt charts, deliverables, milestones, recurring calls, and overall engineering communication with internal and external teams.
  • Support the management of the development engineering project portfolio to ensure adequate resources are available to achieve simultaneous project milestones.
  • Provide informal mentoring and/or supervision to junior team members.
  • Identify raw material suppliers and work toward their approval on Cortland Biomedical's approved supplier list (ASL).
  • Represent Cortland Biomedical as expert in the properties and performance of biomedical textile fibers.
  • Support the creation and validation of test methods for the analysis of design concepts.
  • Ensure project compliance with all ISO 13485 requirements outlined in Cortland Biomedical's Quality Management System. Provide continuous improvement ideas and solutions, in line with Quality initiatives.
  • Develop new technological solutions to manufacturing challenges including identification of new equipment and use of digital tools, where applicable.
  • Support transfer of new product development processes to commercial production.
  • Participate in continuous improvement to improve processes, eliminate problems, streamline operations, or other areas as defined by management.
  • Expand Cortland Biomedical's expertise in state-of-the-art engineering, manufacturing methods, and test methods through technical journals, seminars, advance degree programs, etc.
  • Comply with and participate in safety protocols and initiatives.
  • Additional tasks as assigned.
  • <20% domestic and international travel in support of engineering projects, customers, vendors, conferences, training, etc.

Skills and Competencies
  • Knowledge of the physical and mechanical characteristics of polymers, fibers, yarns, and fabrics preferred
  • Experience with documentation and traceability requirements for highly regulated industries preferred
  • Effective verbal communication skills and comfortable interacting with team members, customers, and vendors at all levels
  • Effective technical writing skills consistent with writing engineering reports and quality management system documentation
  • Demonstrated creative problem solving and effective engineering decision-making skills
  • Experience with Enterprise Resource Platforms (ERP) a plus
  • Demonstrated ability to work well independently and as a team member
  • Self-starter able to work under minimal supervision
  • Capable of generating and delivering internal and external presentations at all levels

Education and Experience
BS Degree in Mechanical, Textile or Biomedical Engineering, or related degree from an accredited university
Minimum of 5 years of experience, 10 years+ preferred, in an engineering function within a manufacturing environment - especially in highly regulated industries (medical device, energy, aerospace, automotive, etc.), medical textiles or medical device preferred.
Physical Demands
Employee may have to lift documents/work materials up to 30 pounds in weight. Employee may have to lift tools up to 50 pounds in weight. Employee will have to be able to walk/climb to a variety of primary work locations, including traveling by air/auto to remote sites. This can include occasional ascending or descending ladders, stairs, scaffolding, ramps, poles, and the like. Employee may move themselves in different positions to accomplish tasks in various environments including tight and confined spaces. Employee will need to move about to accomplish tasks or move from one worksite to another. Employee will need to operate machinery and/or power tools, motor vehicles, and heavy equipment. Employee will need to listen, understand, and speak with team members in person, telephonically, and electronically at all levels within a diverse workforce and with supported organizations. Employee will need to assess the accuracy, neatness, and thoroughness of the work assigned. Employee can work in front of a personal computer and telephone for long periods of time. Will have repetitive motions that include the wrists, hands, and/or fingers.
Work Environment
Primary work environment is temperature-controlled office setting or a controlled manufacturing space but may also be visiting different customers. Specific gowning and PPE requirements will be required when working in different areas. While in the manufacturing space or visiting customers, employee may be exposed to high/low temperatures, outdoor elements (such as precipitation and wind), high levels of noise, hazardous conditions, poor ventilation, small and/or enclosed spaces, or adverse environmental conditions.
The physical demands and work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations will be made to enable individuals with disabilities to perform the essential functions.
Direct Reports
N/A
Key Contacts/Clients
Sales Engineers
Process Engineers
Manufacturing Engineers
Quality Engineers
External Customers
EEO Statement
Enerpac is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, veteran status, or any other protected status in accordance with applicable federal, state, and local laws. We are committed to creating an inclusive environment for all employees and applicants and encourage candidates of all backgrounds to apply.
If you are an individual with a disability and you need assistance or a reasonable accommodation during the application process, please reach out to us at: recruiter@enerpac.com
If you're looking for a unique, exciting career with variety and potential for growth, Enerpac Tool Group offers challenges and rewards for people on a global scale.