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Volunteer Biomedical Product Development Engineer Jobs in Washington

VTG

Product Development Lead

Washington, DC

$130K - $220K/yr

As Product Development Lead, you will assist the U.S. Navy with developing and implementing a ... Bachelor's degree in any technical-related field or engineering field and 15 years professional ...

VTG

Product Development Lead

Washington, DC · On-site

$130K - $220K/yr

As Product Development Lead, you will assist the U.S. Navy with developing and implementing a ... Bachelor's degree in any technical-related field or engineering field and 15 years professional ...

System One

Software Development Engineer (SDET)

Merrifield, VA · On-site

$49.75 - $64.25/hr

Understand project documents, customer demands, and product objectives to create and execute test ... voluntary plans, as well as participation in a 401(k) plan. System One is an Equal Opportunity ...

System One

Software Development Engineer (SDET)

Merrifield, VA · On-site

$49.75 - $64.25/hr

Understand project documents, customer demands, and product objectives to create and execute test ... voluntary plans, as well as participation in a 401(k) plan. System One is an Equal Opportunity ...

System One

Software Development Engineer (SDET)

Merrifield, VA · On-site

$49.75 - $64.25/hr

Understand project documents, customer demands, and product objectives to create and execute test ... voluntary plans, as well as participation in a 401(k) plan. System One is an Equal Opportunity ...

RWD Consulting, LLC

Biomedical Engineer

Bethesda, MD · On-site

$90 - $115/hr

Bachelor of Science in Biomedical Engineering. * Five (5) years' experience in working with ... Formulate monthly reports on production, inventory, quality improvement initiatives, and training ...

RWD Consulting, LLC

Biomedical Engineer

Bethesda, MD · On-site

$90K - $115K/yr

... productivity of the overall timely replacement of technical training equipment within the ... development and conducting of research protocols related to best practices of the training ...

STAGE FRONT

Director of Product Development

Columbia, MD · On-site

$150 - $160/hr

... Product Development to lead the planning, prioritization, and delivery of product initiatives ... This leader will partner closely with Engineering, Operations, Customer Success, Sales, Finance ...

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Volunteer Biomedical Product Development Engineer information

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 are the most commonly searched types of Biomedical Product Development Engineer jobs in Washington?

The most popular types of Biomedical Product Development Engineer jobs in Washington are:

Volunteer Biomedical Product Development Engineer jobs near you

Mechanical Engineer (New Product Development)

Columbia, MD • On-site

Tate
See more jobs at Tateexternal

$75K - $90K/yr

Full-time

Medical, Dental, Vision, Retirement

Re-posted 17 days ago

Job description

Job Type: Full-Time, Exempt
Duration of role: Permanent
Number of Position: 1
Reporting to: New Products Engineering Manager
Location: Columbia, MD/ Glasgow, KY
About Us
At Tate we are passionate about everything we do. As an independent brand operating within Kingspan Group, a global plc group of companies, Tate has been recognized worldwide as an industry leader in the development and manufacture of data center infrastructure solutions and commercial office raised access floors, for over 60 years. With revenues of over $600m and growing, Tate plays a pivotal role in offering expertise in cutting edge design engineering to craft solutions, by working collaboratively with clients as a trusted partner.
Tate continues to grow and expand, operating multiple manufacturing and commercial sites across the US, Europe, the Middle East, Asia, and Australia. We are excited about our fresh, dynamic, and inclusive team of experts working on new innovations and forward-thinking designs, as we remain a market leading player within our industry. We continue to invest heavily in the best available manufacturing tools and equipment needed to adhere to Tate's world class standards and in keeping with our Planet Passionate sustainability strategy, our focus is on having minimal climate impact.
We are excited to potentially welcome you as part of our team as we continue to grow on a worldwide scale.
About the Role
The Mechanical Engineer is responsible for managing new product development, engineering changes, and qualification processes for data center products. This role oversees bills of materials and labor routings for new products and product modifications through prototyping and manufacturing process performance analysis.
The Mechanical Engineer develops quotations for non-standard and new product pricing requests and maintains engineering drawings, specifications, and quality procedure documentation to support product development and manufacturing.
What You'll Do
  • Develop manufacturing processes for new product families in collaboration with production, purchasing, quality, and operations teams.
  • Proactively anticipate potential design changes and incorporate futureproofing where possible.
  • Create quotes for new designs and maintain design history throughout the quoting process.
  • Maintain and update engineering drawings and specifications.
  • Administer processes for new part number creation, bill of material (BOM) updates, labor routing changes, and new product quote requests (excluding MI% data).
  • Interpret project requirements from customers, project managers, or architectural drawings, and communicate feasibility, lead times, and potential challenges.
  • Create project submittal documentation for approval of project design and specifications.
  • Support the manufacturing team with new process development and implementation.
  • Maintain awareness of individual contributions to quality, safety, environmental, and product compliance policies; report all quality issues, unsafe acts, and unsafe conditions to the appropriate personnel.

Additional Expectations
  • Comply with all company policies, including the Code of Conduct and Kingspan Group Compliance Policy.
  • Ensure adherence to applicable laws, regulations, and internal product compliance requirements.
  • Support all activities required to meet Compliance Management System goals.
  • Raise any compliance-related concerns to a supervisor, manager, Leadership Team member, or through the confidential whistleblower service.

What You'll Bring
  • Bachelor's degree in mechanical engineering or another STEM field required.
  • Up to five years of relevant experience in a manufacturing environment preferred.
  • Proficiency in on shape and 2D/3D CAD systems required.
  • Strong proficiency with SolidWorks
  • Experience with AutoCAD and Revit is a plus, particularly BIM (Building Information Modeling).
  • Project management experience is a plus.
  • Familiarity with engineering drawing standards, new product development, and manufacturing processes and controls preferred.
  • Strong attention to detail.
  • Proficiency with Microsoft Office 365 (Word, Excel, Teams, etc.).
  • Excellent verbal and written communication skills.
  • Strong organizational and time-management abilities.
  • Ability to work effectively in a fast-paced environment and adapt to changing project requirements.

What You'll Get
  • Pay range: $75,000 to $90,000 USD per year. This role is eligible for a discretionary bonus.
  • Career Scope and Advancement: As we grow, new positions and career opportunities arise, offering accelerated paths for the right candidates, locally and globally.
  • World of Wellness Philosophy: We empower you to take charge of your health and well-being. You'll have access to a wide range of medical, dental, and vision benefits, along with personalized guidance from a "Health Advocate." We also offer other supplemental options, including 401k, legal, disability, and theft insurance, to ensure your financial wellness.
  • Corporate Social Responsibility: Through Planet Passionate we are determined to reduce our manufacturing carbon (CO2e) emissions to as close to zero as technically possible, together with halving carbon intensity in our primary supply chain. We are very involved in our community, and you will have ample opportunities to support us in creating a better world.
  • Skills Development: Given the dynamic pace of our business and a strong collaborative environment, your new role will be diverse and multifaceted - allowing you to be more versatile and develop a broader skill set.
  • Mentorship and development: At Tate, we don't believe in hierarchy, we work together as one team for one common goal. You will have access and exposure to our senior leaders and experts for learning in your role, and additionally mentorship for the future.
  • Culture: We have a great team culture, highly collaborative, supportive, and social. Together we innovate, collaborate, take ownership, and strive for excellence.

Stay connected with us on LinkedIn for insights into life at Tate. Join us in our mission to make a difference through exceptional solutions.
Tate Inc. is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to legally protected characteristics. We are committed to providing reasonable accommodations to qualified individuals with disabilities. Employment is contingent upon the successful completion of post-offer requirements, including a background check and drug screening, in accordance with company policy and applicable laws.
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Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws.
For further information, please review the Know Your Rights notice from the Department of Labor.

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