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Contract Biomedical Product Development Engineer Jobs in Georgia

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Contract Biomedical Product Development Engineer information

What is the difference between Contract Biomedical Product Development Engineer vs Contract Biomedical Research Scientist?

AspectContract Biomedical Product Development EngineerContract Biomedical Research Scientist
CredentialsBachelor's or Master's in Biomedical Engineering, related fieldBachelor's or Master's in Biology, Biomedical Science, or related field
Work EnvironmentDesign, develop, and test medical devices and products in R&D labs or manufacturing settingsConduct experiments, analyze biological data, and study disease mechanisms in research labs
Employer & Industry UsageMedical device companies, biotech firms, healthcare product developersResearch institutions, biotech companies, pharmaceutical firms

The Contract Biomedical Product Development Engineer focuses on designing and developing medical devices and products, working closely with engineering teams. In contrast, the Contract Biomedical Research Scientist conducts biological research to understand disease processes or test biological hypotheses. Both roles require scientific credentials but differ in their primary focus and work environment.

What does a Contract Biomedical Product Development Engineer do?

A Contract Biomedical Product Development Engineer is a specialized professional who works on a temporary or project basis to design, develop, and improve medical devices and products. They collaborate with multidisciplinary teams to ensure products meet regulatory standards, are safe for patients, and function as intended. Their responsibilities often include prototyping, testing, and documenting development processes, as well as troubleshooting and refining designs based on feedback and test results. This role is vital for bringing innovative healthcare solutions to market efficiently and effectively.

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

To thrive as a Contract Biomedical Product Development Engineer, you need a strong background in biomedical engineering principles, product design, and regulatory compliance, usually supported by a relevant engineering degree. Familiarity with CAD software, prototyping tools, and standards such as ISO 13485 or FDA regulations is typically required. Exceptional problem-solving, project management, and collaboration skills help you drive projects forward and adapt quickly in dynamic environments. Mastery of these skills ensures innovative, safe, and compliant medical products are developed efficiently to meet client and regulatory expectations.

How does a Contract Biomedical Product Development Engineer typically interact with cross-functional teams during a project?

As a Contract Biomedical Product Development Engineer, you will regularly collaborate with cross-functional teams, including regulatory affairs, quality assurance, manufacturing, and clinical teams. You may participate in design reviews, coordinate testing protocols, and ensure that the product meets both engineering and compliance standards. Effective communication and documentation are essential, as you often serve as a liaison between technical and non-technical stakeholders. These collaborations help streamline the development process and ensure that project milestones are met on time.
What are the most commonly searched types of Biomedical Product Development Engineer jobs in Georgia? The most popular types of Biomedical Product Development Engineer jobs in Georgia are:
Contract Biomedical Product Development Engineer jobs near you
Senior Product Development Engineer

Senior Product Development Engineer

Femasys, Inc.

Suwanee, GA

Full-time

Posted 5 days ago

Job description

We are looking for a Senior Product Development Engineer who thrives in a small, fast-paced environment and wants to play a hands-on role in bringing innovative medical devices from concept to market. This is not a narrowly defined role—you will be expected to take ownership, operate across design, testing, and development activities, and directly influence product and process outcomes.
Key Responsibilities:
  • Lead product development efforts from early concept through commercialization with a strong focus on execution.
  • Design and iterate components and assemblies using SolidWorks with minimal oversight.
  • Develop, build, and troubleshoot prototypes and test setups in a hands-on manner.
  • Design and qualify equipment (IQ/OQ/PQ) to support both development and early manufacturing.
  • Work closely with Manufacturing, Quality, and Regulatory to ensure practical, compliant solutions.
  • Identify issues quickly and drive resolution without relying on large support teams.
  • Generate and maintain design control documentation in alignment with FDA and ISO requirements.
  • Support design transfer and early production, including time on the manufacturing floor.
What We’re Looking For:
  • An engineer who is comfortable operating with limited structure and high ownership.
  • A practical problem-solver who can balance speed with quality and compliance.
  • A team player who communicates directly and effectively in a small group setting.
Qualifications:
  • Bachelor’s or Master’s degree in Mechanical Engineering, Biomedical Engineering, or similar.
  • 5+ years of product development experience, ideally in the medical device industry.
  • Strong proficiency in SolidWorks.
  • Experience with equipment design and qualification (IQ/OQ/PQ).
  • Working knowledge of design controls and FDA/ISO 13485 requirements.
  • Demonstrated success in a small company, startup, or similar resource-constrained environment.
Preferred Experience:
  • Experience with catheter-based or minimally invasive devices.
  • Familiarity with processes such as extrusion, bonding, and assembly of disposable medical devices.
  • Experience supporting early manufacturing scale-up.

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