ZipRecruiter

Log In

1

Contract Biomedical Product Development Engineer Jobs in Georgia

CKS Packaging

Product Development Engineer

Atlanta, GA · On-site

Product Development Engineer Needed- Atlanta, GA (Please note if you are viewing this posting on an external job board, unless specifically stated in the posting, the provided hourly/salary estimates ...

next page

Showing results 1-20

All JobsContract Biomedical Product Development Engineer JobsContract Biomedical Product Development Engineer Jobs in Georgia

Contract Biomedical Product Development Engineer information

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.

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 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.

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.

Contract Biomedical Product Development Engineer jobs near you

Senior Product Development Engineer

Filtration Group Corp

Fairburn, GA • On-site

Full-time

Re-posted 26 days ago

Filtration Group rating

6.6

Company rating: 6.6 out of 10

Based on 11 frontline employees who took The Breakroom Quiz

Job description

Porex is a global leader in developing custom-engineered porous polymer solutions that turn into high-value functional components in our customers’ end products. Porex is trusted for unique components across a wide variety of device applications in the life sciences, consumer, and electronics markets to give products a competitive edge. For more information, visit www.porex.com .

We are seeking an experienced and self-driven Advanced Product Development Engineer to lead and support the development of next-generation porous material solutions and engineered components across diagnostics, medical, personal care, and industrial markets. This role will serve as a technical bridge between R&D, commercial teams, and manufacturing, driving prototype development, product validation, and design transfer to ensure smooth transition from concept to commercial product. The ideal candidate will bring strong product development fundamentals, excellent communication skills, and hands-on experience in material-based product design, performance testing, and customer-facing technical support.


  • Lead product development projects from concept through commercialization, working with cross-functional teams (R&D, manufacturing, QA, commercial, regulatory).
  • Translate customer and market requirements into engineering specifications and material/component designs.
  • Drive prototype development, iteration, and performance validation using in-house and customer-supplied testing protocols.
  • Partner with Advanced Materials Engineering team to incorporate new materials and surface modifications into product design.
  • Lead design for manufacturability (DFM) and design transfer processes to scale from lab to production.
  • Conduct risk assessments, design reviews, and verification/validation activities in accordance with internal and customer quality systems.
  • Coordinate with QA and Regulatory teams to ensure new products meet relevant standards (e.g., ISO 10993, USP Class VI, FDA 21 CFR).
  • Document technical data, create test protocols and reports, and contribute to technical files for internal records and external submissions.
  • Participate in customer engagements, joint development discussions, application mapping, and field performance evaluations.
  • Contribute to intellectual property development (patents, trade secrets) based on novel designs or applications.

  • Bachelor's or master's degree (preferred) in Mechanical engineering, Biomedical Engineering, Materials Science, or related fields.
  • 5+ years of industry experience in product development, preferably in medical devices, diagnostics, or engineered polymer components.
  • Solid understanding of polymer materials, compounding additives, surface coatings, porous media, membranes, or filtration systems is highly desirable.
  • Proven experience with design verification & validation, risk analysis (FMEA), and design documentation.
  • Familiarity with CAD tools (e.g., SolidWorks) and working with prototypes, fixtures, and custom test setups.
  • Working knowledge of regulatory and quality requirements for medical and diagnostics product development.
  • Strong analytical and problem-solving skills; ability to interpret test results and propose design improvements.
  • Excellent written and verbal communication skills with ability to present technical content to diverse audiences.
  • Collaborative mindset with ability to work independently and drive cross-functional alignment.

What Filtration Group employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom

Apply