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Biomedical Manufacturing Jobs in Georgia (NOW HIRING)

Ensure adherence to design standards, processes, and Design for Manufacturing (DFM) principles ... Biomedical Engineering (ABET preferred) or equivalent experience

Fluid Mechanics Design Engineer

Atlanta, GA · On-site

$73K - $99K/yr

Partner with suppliers to ensure design for manufacturing (DFM) and project alignment ... Bachelor's degree in Mechanical, Mechatronics, Aerospace, Biomedical Engineering , or related field ...

Lead DFM/DFX discussions with customers to optimize designs for manufacturability, scalability, and ... Bachelor's degree in Mechanical, Biomedical, or related Engineering field (Master degree is ...

Showing results 41-60

Biomedical Manufacturing information

What is the difference between Biomedical Manufacturing vs Medical Device Assembly?

AspectBiomedical ManufacturingMedical Device Assembly
Required CredentialsHigh school diploma or equivalent; certifications varyHigh school diploma or equivalent; often similar certifications
Work EnvironmentFactories, cleanrooms, laboratoriesFactories, cleanrooms, laboratories
Employer & Industry UsageBiotech firms, pharmaceutical companies, medical device manufacturersMedical device companies, healthcare equipment manufacturers
Common Search & Comparison IntentUnderstanding roles in biomedical manufacturingDifferences between assembly roles in medical device production

Biomedical Manufacturing involves the production of a wide range of medical products, including drugs, biologics, and devices, often requiring specialized equipment and processes. Medical Device Assembly specifically focuses on assembling medical devices, emphasizing precision and quality control. While both roles share similar environments and credentials, Biomedical Manufacturing covers a broader scope, whereas Medical Device Assembly is more specialized in device construction.

What are some common challenges faced in a biomedical manufacturing role, and how can new employees prepare for them?

In biomedical manufacturing, one common challenge is adhering to strict regulatory standards and quality control protocols, such as Good Manufacturing Practices (GMP). New employees may also find the need for meticulous documentation and routine audits demanding. To prepare, it's helpful to familiarize yourself with industry regulations and standard operating procedures, and to develop strong attention to detail. Additionally, being comfortable working both independently and as part of a cross-functional team will help you adapt to the collaborative nature of most biomedical manufacturing environments.

What is biomedical manufacturing?

Biomedical manufacturing is the process of producing medical devices, equipment, and components used in healthcare and life sciences. This field combines engineering, biology, and manufacturing principles to create products like implants, diagnostic tools, prosthetics, and surgical instruments. The process often involves strict regulatory standards to ensure safety and efficacy. Biomedical manufacturing plays a crucial role in advancing medical technology and improving patient care.

What are the key skills and qualifications needed to thrive in biomedical manufacturing?

To thrive in Biomedical Manufacturing, you need a solid background in biomedical engineering or life sciences, with knowledge of manufacturing processes and regulatory standards like GMP. Familiarity with laboratory equipment, quality control systems, and software such as CAD or ERP is typically required. Attention to detail, problem-solving abilities, and effective teamwork are crucial soft skills in this field. These competencies ensure the safe, efficient, and compliant production of biomedical products that meet industry and patient needs.
What are the most commonly searched types of Biomedical Manufacturing jobs in Georgia? The most popular types of Biomedical Manufacturing jobs in Georgia are:
Infographic showing various Biomedical Manufacturing job openings in Georgia as of July 2026, with employment types broken down into 89% Full Time, 3% Part Time, 1% Temporary, 3% Contract, and 4% Nights. Highlights an 96% Physical, 2% Hybrid, and 2% Remote job distribution.

Senior Product Development Engineer

Femasys, Inc.

Suwanee, GA

Full-time

Re-posted 14 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.