Medical Devices STEM OPT Jobs in Georgia
Medical devices F-1 STEM OPT sponsorship jobs in Georgia are concentrated around Atlanta and the broader metro corridor, where employers like Becton Dickinson, Stryker, and Medline Industries maintain significant operations. Georgia's growing medtech sector, anchored by research institutions and hospital networks, supports roles in biomedical engineering, regulatory affairs, and quality systems that qualify for STEM OPT authorization.
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Get Access To All JobsINTRODUCTION
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 & Development (R&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&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.
BASIC QUALIFICATIONS:
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
INTRODUCTION
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 & Development (R&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&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.
BASIC QUALIFICATIONS:
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
STEM OPT Medical Devices Job Roles in Georgia
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Search Medical Devices Jobs in GeorgiaMedical Devices STEM OPT Sponsorship Jobs in Georgia: Frequently Asked Questions
Which medical devices companies sponsor F-1 STEM OPT visas in Georgia?
Georgia-based medical devices employers with documented STEM OPT sponsorship activity include Becton Dickinson, which operates facilities in the Atlanta metro area, along with Stryker, Medline Industries, and smaller medtech firms clustered near Emory University and Georgia Tech. Hospital-adjacent device manufacturers and contract research organizations in the state also participate in STEM OPT authorization, particularly for engineering and quality assurance roles.
Which cities in Georgia have the most medical devices F-1 STEM OPT sponsorship jobs?
Atlanta accounts for the largest share of medical devices STEM OPT sponsorship activity in Georgia, driven by its concentration of hospital systems, research universities, and corporate headquarters. Decatur and Norcross host device manufacturing and distribution operations, while the Athens corridor benefits from University of Georgia research partnerships. Savannah has seen emerging medtech activity tied to its expanding advanced manufacturing base.
What types of medical devices roles typically qualify for F-1 STEM OPT sponsorship?
Roles that commonly qualify for STEM OPT sponsorship in the medical devices industry include biomedical engineering, quality engineering, regulatory affairs, manufacturing engineering, software engineering for embedded medical systems, and research and development positions. These roles typically require a STEM-designated degree such as biomedical engineering, electrical engineering, or computer science, and must fall under an employer enrolled in E-Verify as required by STEM OPT regulations.
How do I find medical devices F-1 STEM OPT sponsorship jobs in Georgia?
Migrate Mate is built specifically to surface medical devices jobs with verified STEM OPT sponsorship history in Georgia, filtering by employers who have filed the necessary labor condition documentation. Rather than sorting through general job listings, you can search directly for Georgia-based medtech roles at companies with active F-1 STEM OPT authorization patterns, saving significant time in identifying employers who are already set up to support your work authorization.
Are there state-specific considerations for F-1 STEM OPT sponsorship in Georgia's medical devices industry?
Georgia does not impose state-level visa sponsorship requirements beyond federal STEM OPT rules, but the state's medical devices employers are subject to FDA regulatory oversight that shapes hiring timelines and role structures. Companies pursuing FDA clearance or approval cycles often have longer onboarding processes, which can affect STEM OPT start dates. Georgia's E-Verify participation rate among manufacturing employers is high, which is a federal prerequisite for any STEM OPT extension.