1

Medical Device Integration Jobs in Georgia (NOW HIRING)

... device industries with a proven, scientific approach to complex trial data and regulatory ... forms, integrated safety and efficacy summaries, Module 2.7.1, 2.7.2, 2.7.3, 2.7.4, and 2.5 ...

... care medical device solutions used in the detection of infectious disease such as COVID-19 ... Technology Integration Drive the adoption of automation, and other advanced technologies to improve ...

... care medical device solutions used in the detection of infectious disease such as COVID-19 ... Technology Integration Drive the adoption of automation, and other advanced technologies to improve ...

... care medical device solutions used in the detection of infectious disease such as COVID-19 ... Technology Integration Drive the adoption of automation, and other advanced technologies to improve ...

Showing results 21-40

Medical Device Integration information

What is a medical device integration?

A Medical Device Integration job involves connecting medical devices to healthcare IT systems, such as electronic health records (EHRs), to ensure seamless data exchange. Professionals in this role configure, test, and troubleshoot interfaces between devices and software to improve clinical workflows and patient care. They work closely with biomedical engineers, IT specialists, and healthcare providers to ensure reliable and accurate data transmission. Strong technical knowledge of interoperability standards like HL7, DICOM, and FHIR is often required.

What are some common challenges faced in medical device integration roles?

Professionals in Medical Device Integration often encounter challenges such as managing compatibility across diverse devices and systems, troubleshooting intermittent connectivity issues, and complying with strict health data security regulations. The role frequently involves working with cross-functional teams, including IT, clinical staff, and device manufacturers, which requires clear communication and collaboration. Additionally, the rapid pace of technological advancements means team members must continually update their knowledge and adapt to new standards. Overcoming these challenges is not only rewarding but also critical to delivering seamless interoperability and improving clinical workflows.

What are the key skills and qualifications needed to thrive in medical device integration?

To thrive in Medical Device Integration, you need a solid understanding of medical devices, networking, HL7 interfaces, and healthcare IT systems, often supported by a degree in biomedical engineering, information technology, or a related field. Familiarity with integration engines (such as Mirth Connect or Cloverleaf), EHR platforms, and relevant certifications like CBET or CHTM is highly beneficial. Strong problem-solving, teamwork, and communication skills help in collaborating with clinicians, vendors, and IT staff. These competencies are essential for ensuring reliable and secure data flow between devices and healthcare systems, ultimately supporting patient care and operational efficiency.

What cities in Georgia are hiring for Medical Device Integration jobs? Cities in Georgia with the most Medical Device Integration job openings:
Infographic showing various Medical Device Integration job openings in Georgia as of August 2026, with employment types broken down into 1% As Needed, 76% Full Time, 16% Part Time, 1% Temporary, and 6% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution.

Continuous Improvement/Integration Engineer

Femasys, Inc.

Suwanee, GA โ€ข On-site

$73K - $98K/yr

Full-time

Re-posted 2 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 & 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.

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