Manufacturing Engineer — Medical Device; Onsite — Johns Creek, GA Temp

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

From development to commercialization, we partner with Pharmaceutical, Medical Device and Biotechnology clients to provide solutions to complex compliance issues. We collaborate with our partners by providing technical expertise in Quality, Regulatory Compliance and Manufacturing Science and Technology. Our business mission is to ensure our clients exceed their compliance goals while improving patient health and safety. Visit us at  and follow us on Linked In:

Our Fortune 500 Medical Device client has an exciting opportunity for aManufacturing 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
• Exposure to manufacturing systems (e.g., MES, SAP)
• Basic familiarity with automated equipment and controls
• 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

Pharmavise Corporation is an Equal Opportunity Employer and does not discriminate on the basis of race or ethnicity, religion, sex, national origin, age, veteran disability or genetic information or any other reason prohibited by law in employment.