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Temporary R&D Engineer Medical Device Jobs in Atlanta, GA

ATL Technology

Application Engineer

Atlanta, GA

POSITION SUMMARY The Application Engineer serves as a key technical partner to the sales, costing, sourcing, and commercial teams, helping to secure and grow business with our medical device OEM ...

Wise Skulls

Embedded Engineer

Atlanta, GA · On-site

$125K - $165K/yr

Prior experience in medical device product development. * Ability to integrate .NET applications with firmware and hardware components.

MLS Technologies

Embedded Firmware Engineer

Ball Ground, GA · On-site

$96K - $131K/yr

The Firmware Engineer will be responsible for providing cross-functional engineering project ... Familiarity with the Medical Device Directive/Regulation (MDD/MDR), ISO 13485, FDA design controls ...

SGS

Sr. Sales Executive - Medical Device

Suwanee, GA · On-site +1

Bachelor's degree or equivalent educational background in Analytical Sciences, Engineering ... Health: Medical, dental and vision insurance, life insurance, employee assistance programs.

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All JobsR&D Engineer Medical Device JobsTemporary R&D Engineer Medical Device JobsTemporary R&D Engineer Medical Device Jobs in Atlanta, GA

Temporary R D Engineer Medical Device information

What is the difference between Temporary R&D Engineer Medical Device vs Temporary Quality Engineer Medical Device?

AspectTemporary R&D Engineer Medical DeviceTemporary Quality Engineer Medical Device
Primary FocusResearch and development of new medical device productsEnsuring product quality and compliance with standards
Required SkillsDesign, prototyping, testing, and engineering analysisQuality assurance, regulatory compliance, inspection processes
Work EnvironmentDesign labs, R&D departments, product development teamsQuality control labs, regulatory departments, manufacturing sites
Common CertificationsEngineering degrees, CAD, prototyping skillsISO standards, GMP, quality management certifications

While both roles support medical device companies, the Temporary R&D Engineer Medical Device focuses on developing and testing new products, whereas the Temporary Quality Engineer Medical Device emphasizes maintaining product quality and regulatory compliance. Understanding these differences helps candidates target the right roles based on their skills and career goals.

What are the most commonly searched types of R&D Engineer Medical Device jobs in Atlanta, GA? The most popular types of R&D Engineer Medical Device jobs in Atlanta, GA are:
Temporary R D Engineer Medical Device jobs near you
Infographic showing various Temporary R&D Engineer Medical Device job openings in Atlanta, GA as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, and 6% Contract. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution.

Continuous Improvement/Integration Engineer

Femasys, Inc.

Suwanee, GA • On-site

$73K - $98K/yr

Full-time

Re-posted 3 days ago

Job description

We are looking for a Continuous Improvement/Integration 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 position is based in our Suwanee, Georgia office and is responsible for supporting the integration of new products into manufacturing while driving ongoing improvements in product efficiencies and cost-effectiveness. This role focuses on enhancing manufacturing processes through simplification, waste reduction, automation, and cost-saving initiatives. Key responsibilities include reducing scrap, lowering material costs, increasing operational efficiency, and implementing sustainable process improvements to support high-quality and cost-efficient production.
Core Responsibilities:
  • Develop, implement, and validate manufacturing processes and equipment to support efficient and high-quality product production
  • Update INFOR Bills of Materials (BOMs) and cost standards for both existing and new products
  • Conduct time studies as needed to establish accurate manufacturing standards and identify opportunities for efficiency improvements
  • Collaborate closely with Research amp; Development (R amp;D) team to ensure smooth transition of new projects into manufacturing operations
  • Promote a culture centered on customer satisfaction, quality initiatives, and continuous improvement
  • Develop and maintain key quality and cost metrics, and proactively pursue cost savings through lean manufacturing, process optimization, and capital investments
  • Ensure compliance with applicable FDA and ISO regulations, particularly in the areas of traceability, equipment maintenance, and process validation
  • Uphold facility cleanliness and housekeeping standards to support a safe and efficient work environment
  • Partner with R amp;D, Marketing, and Quality teams on product enhancements or modifications to ensure designs are optimized for manufacturability
  • Maintain a safe work environment in compliance with all relevant federal and state health and safety regulations
  • Implement mistake-proofing strategies (poka-yoke) to minimize the risk of quality defects
  • Collaborate with suppliers to enhance the quality and robustness of incoming materials and reduce nonconformances
  • Establish and manage systems to track scrap, rework, and nonconformances, with the goal of reducing manufacturing costs over time
  • Work is performed in a normal manufacturing environment with exposure to production equipment and materials
  • Must be able to sit, stand, walk, bend, and move about for extended periods throughout the work day. Ability to lift and carry light to moderately heavy materials as needed.
  • Must be able to access a cleanroom and use personal protective equipment (PPE) properly throughout the day. Most work will be completed within a controlled cleanroom environment.
What We’re Looking For:
Required:
  • Bachelor’s degree in a technical field and/or 5+ years of manufacturing experience
  • Lean and/or Six Sigma experience
  • Experience utilizing a Quality System and ERP System
  • Knowledge of GMP regulatory requirements
  • Ability to solve problems and implement project plans
Preferred:
  • Bachelor of Science in Engineering field
  • Experience using INFOR as an ERP system
  • Holds Lean/Six Sigma Certification
  • 3+ years’ experience in a Class III medical device manufacturer
  • Medical design engineering experience

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