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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 ...

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Biomedical Product Development Engineer information

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$33.4K

$74.2K

$111.9K

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

As of Sep 6, 2026, the average yearly pay for biomedical product development engineer in Georgia is $74,208.00, according to ZipRecruiter salary data. Most workers in this role earn between $60,800.00 and $84,400.00 per year, depending on experience, location, and employer.

What does a biomedical product development engineer do?

A Biomedical Product Development Engineer is responsible for designing, developing, and testing medical devices and healthcare-related products. They collaborate with cross-functional teams, including scientists, regulatory specialists, and manufacturing engineers, to ensure products meet safety and regulatory standards. Their work involves prototyping, conducting validation studies, and optimizing designs for production. Additionally, they stay updated on industry advancements and compliance requirements to bring innovative solutions to market.

What are the key skills and qualifications needed to thrive as a biomedical product development engineer?

To thrive as a Biomedical Product Development Engineer, you need a solid background in biomedical engineering, product design, and regulatory compliance, usually supported by a relevant engineering degree. Familiarity with CAD software, simulation tools, FDA regulations, and ISO standards is highly valuable, and some roles may require certification such as a Professional Engineer (PE) license. Excellent problem-solving skills, creativity, project management abilities, and effective communication are key soft skills that distinguish top performers in this field. These competencies ensure the successful development, testing, and delivery of safe and innovative biomedical devices that meet industry standards.

What are the typical challenges a biomedical product development engineer faces when bringing a new medical device to market?

Biomedical Product Development Engineers often encounter challenges such as navigating complex regulatory requirements, integrating multidisciplinary feedback, and ensuring device safety and efficacy through rigorous testing. Balancing innovative design with manufacturability and cost constraints is common, especially when working under tight deadlines. Collaboration with clinicians, quality assurance teams, and regulatory affairs professionals is an essential part of the process. Adapting quickly to feedback and addressing unforeseen technical issues are key to successfully advancing a product from concept to commercialization.

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:

What are popular job titles related to Biomedical Product Development Engineer jobs in Georgia?

For Biomedical Product Development Engineer jobs in Georgia, the most frequently searched job titles are:

What job categories do people searching Biomedical Product Development Engineer jobs in Georgia look for?

The top searched job categories for Biomedical Product Development Engineer jobs in Georgia are:

What cities in Georgia are hiring for Biomedical Product Development Engineer jobs?

Cities in Georgia with the most Biomedical Product Development Engineer job openings:

Biomedical Product Development Engineer jobs near you
Infographic showing various Biomedical Product Development Engineer job openings in Georgia as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 16% Part Time, and 3% Contract. Highlights an 91% Physical, 3% Hybrid, and 6% Remote job distribution, with an average salary of $74,208 per year, or $35.7 per hour.

Senior Product Development Engineer

Filtration Group Corp

Fairburn, GA • On-site

$120 - $180/hr

Other

Re-posted yesterday

Filtration Group rating

6.6

Company rating: 6.6 out of 10

Based on 11 frontline employees who took The Breakroom Quiz

Job description

Overview

Porex is on a mission to make the world safer, healthier and more productive. 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.

Responsibilities
  • 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.
Qualifications
  • 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.
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