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Medical Device Manufacturing Engineer Jobs in Atlanta, GA

Must have 4 years of experience in a facilities engineering role working in a medical device manufacturing environment. * Must include experience working within cGMP, ISO and FDA regulations ...

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We are an innovative, Denmark-based medical device manufacturer specializing in clinical and ... Qualifications: * Background in biomedical engineering, life sciences, neuroscience, BMET or ...

Manufacturing Engineer

Marietta, GA · On-site

$69K - $89K/yr

Manufacturing Engineer is responsible for technically supporting all the operations. Responsible ... Comprehensive medical, dental and vision insurance plan * Paid holidays and vacation * 401K plan

Education: Bachelor's degree in Engineering, Life Sciences, Business, or a related field ... Technical background with a solid understanding of medical device manufacturing. * Demonstrated ...

Manufacturing Engineer

Hiram, GA · On-site

$64K - $82K/yr

POSITION PURPOSE The Manufacturing Engineer's responsibilities include identifying areas for ... medical needs due to pregnancy, child birth or other medical conditions), national origin, age ...

The Cost Engineer is responsible for developing accurate and comprehensive cost calculations for ... Previous experience in high‑ tech/semiconductor, aerospace, or medical device manufacturing ...

Application Engineer

Atlanta, GA · On-site

$100 - $120/hr

Position Summary The Application Engineer serves as a key technical partner to the sales, costing ... Stay informed on emerging trends in medical device technologies and manufacturing solutions to ...

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Showing results 1-20

Medical Device Manufacturing Engineer information

See Atlanta, GA salary details

$45.7K

$82.3K

$115.4K

How much do medical device manufacturing engineer jobs pay per year?

As of Aug 28, 2026, the average yearly pay for medical device manufacturing engineer in Atlanta, GA is $82,331.00, according to ZipRecruiter salary data. Most workers in this role earn between $70,200.00 and $90,400.00 per year, depending on experience, location, and employer.

What does a medical device manufacturing engineer do?

A Medical Device Manufacturing Engineer is responsible for designing, developing, and optimizing manufacturing processes for medical devices. They ensure that products are produced efficiently, safely, and in compliance with regulatory standards such as FDA or ISO guidelines. Their work involves collaborating with design teams, troubleshooting production issues, implementing quality control procedures, and continuously improving manufacturing methods to enhance product quality. Ultimately, they play a key role in bringing safe and effective medical devices to market.

What are the key skills and qualifications needed to thrive as a medical device manufacturing engineer?

To excel as a Medical Device Manufacturing Engineer, you need a solid background in engineering principles, manufacturing processes, and regulatory compliance, typically supported by a degree in biomedical, mechanical, or industrial engineering. Familiarity with CAD software, Six Sigma/Lean methodologies, and knowledge of FDA or ISO 13485 standards is essential. Strong problem-solving, teamwork, and communication skills help manage cross-functional projects and ensure product quality. These competencies are crucial for developing safe, effective devices in a highly regulated industry where precision and compliance are paramount.

What are some common challenges faced by medical device manufacturing engineers during product development?

Medical Device Manufacturing Engineers often encounter challenges in balancing strict regulatory compliance with efficient production processes. Adapting to frequent design changes, ensuring high product quality, and validating manufacturing processes are crucial tasks. Additionally, they collaborate closely with cross-functional teams—including quality assurance, R&D, and supply chain—to troubleshoot production issues and implement improvements. Addressing these challenges requires strong problem-solving skills and a keen attention to detail.

What is the difference between Medical Device Manufacturing Engineer vs Quality Assurance Engineer?

AspectMedical Device Manufacturing EngineerQuality Assurance Engineer
CredentialsBachelor's in engineering or related field; certifications like ASQ CQE beneficialBachelor's in engineering, quality assurance, or related; certifications like ASQ CQE or CQA common
Work EnvironmentManufacturing plants, production lines, R&D labsQuality labs, manufacturing sites, regulatory agencies
Industry UsageDesign, develop, and optimize manufacturing processesEnsure product quality, compliance, and process improvements

While both roles work within the medical device industry and require similar credentials, the Medical Device Manufacturing Engineer focuses on manufacturing processes and product development, whereas the Quality Assurance Engineer emphasizes maintaining quality standards and regulatory compliance.

What are popular job titles related to Medical Device Manufacturing Engineer jobs in Atlanta, GA?

For Medical Device Manufacturing Engineer jobs in Atlanta, GA, the most frequently searched job titles are:

What job categories do people searching Medical Device Manufacturing Engineer jobs in Atlanta, GA look for?

The top searched job categories for Medical Device Manufacturing Engineer jobs in Atlanta, GA are:

Infographic showing various Medical Device Manufacturing Engineer job openings in Atlanta, GA as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 16% Part Time, 5% Contract, and 1% Nights. Highlights an 86% Physical, 1% Hybrid, and 13% Remote job distribution, with an average salary of $82,331 per year, or $39.6 per hour.

Manufacturing Engineer - Medical Device (Onsite - Johns Creek, GA) Possible Temp-to-Hire

Pharmavise

Duluth, GA • On-site

$67K - $86K/yr

Contractor

Re-posted 12 days ago


Job description


Our Fortune 500 Medical Device client has an exciting opportunity for a Manufacturing Engineer.
Job Summary
Responsible for sustaining and improving manufacturing processes and semi-automated equipment to support safe, compliant, and efficient production within a regulated environment.
Key Responsibilities
• Maintain and continuously improve established manufacturing processes, tooling, and semi-automated systems
• Own equipment performance, reliability, and long-term sustainability
• Troubleshoot mechanical and electrical issues using structured root cause methodologies
• Drive equipment and process improvements, including error-proofing and uptime optimization
• Execute validation activities (IQ/OQ/PQ) and maintain technical documentation
• Ensure compliance with FDA, ISO, and internal quality system requirements
• Support CAPA, nonconformance investigations, and audit readiness
• Provide real-time production support and drive continuous improvement initiatives
• Train and guide technicians and operators on processes and equipment
Basic Qualifications
• Bachelor's degree in mechanical, Electrical, or related Engineering discipline
• 2+ years of engineering experience in a regulated manufacturing environment
• Hands-on experience with mechanical systems, equipment, and tooling
• Electrical troubleshooting and controls fundamentals
• Experience supporting or owning semi-automated manufacturing equipment
• Strong problem-solving and root cause analysis capability
Preferred Qualifications
• Medical device manufacturing experience
• Experience with validation processes (IQ/OQ/PQ) and quality systems
• Lean / Six Sigma experience
• Exposure to manufacturing systems (e.g., MES, SAP)
• Basic familiarity with automated equipment and controls
Key Competencies
• Technical problem solving - track record of resolving technical problems using critical thinking skills and proven methodologies (6-step problem-solving, DMAIC, etc.)
• Cross-functional collaboration - can work collaboratively with other functions and encourages transparency, feedback, and respectful disagreements/challenges all for the greater good of improving the production unit, site, and ultimately the company.
• Ownership and accountability -drive individually owned tasks to completion within the timeframe aligned with team or management, fully understands and owns the role of an ME, owns up to mistakes and failures and is transparent about it but also strives to resolve and rectify mistakes
• Continuous improvement mindset - willingness to always be learning and improving oneself, their team, and their production unit
• Ability to learn quickly - not afraid to fail fast and learn from mistakes; willingness to learn new things quickly and correctly apply learnings
Other Details
Schedule: 08:00:AM - 04:30:PM
Work Setup: Onsite - Johns Creek, GA
Contract Length: 6 Months (7/20/2026 - 1/19/2027) Possible Contract Extension or Temp-to-Hire