Quality Engineer I

This role works closely with Manufacturing, Engineering, Supply Chain, and other cross-functional partners to support day-to-day production, investigate quality issues, maintain compliance with the Quality System, and drive continuous improvement. Experience or coursework related to Quality Engineering, Manufacturing Engineering, Biomedical Engineering, Mechanical Engineering, Electrical Engineering, or a related discipline.

Our client, a Medical Device and Healthcare company, is looking for a Quality Engineer I for their Atlanta, GA location.
 
Responsibilities:

• The Quality Engineer I (QE I) supports manufacturing operations by helping ensure products and processes consistently meet quality, regulatory, and business requirements.
• This role works closely with Manufacturing, Engineering, Supply Chain, and other cross-functional partners to support day-to-day production, investigate quality issues, maintain compliance with the Quality System, and drive continuous improvement.
• Provide Quality Engineering support for day-to-day manufacturing operations and production activities.
• Review manufacturing documentation and records to ensure compliance with approved procedures, specifications, and quality requirements.
• Support the identification, documentation, investigation, and resolution of manufacturing quality issues.
• Initiate and support Nonconforming Material Reports (NCMRs) and other quality records, including investigation and disposition activities.
• Participate in root cause investigations and support implementation of corrective and preventive actions.
• Support manufacturing process changes, validations, qualifications, and continuous improvement activities.
• Support audit and inspection readiness and assist with internal and external audit activities as needed.
• Ensure activities are performed in accordance with applicable procedures, Quality System requirements, and regulatory standards.
• Perform other Quality Engineering responsibilities as assigned.

 
Requirements:

• Bachelor’s degree in Engineering, Science, or another related technical discipline, or an equivalent combination of education and relevant technical experience.
• 0–2 years of experience in Quality, Engineering, Manufacturing, Operations, or another related technical field.
• Demonstrated ability to analyze information, solve problems, and make sound decisions using available data.
• Strong written and verbal communication skills.
• Ability to work effectively in a cross-functional, team-based manufacturing environment.
• Strong attention to detail and organizational skills.
• Ability and willingness to learn manufacturing processes, quality systems, and regulatory requirements.
• Internship, co-op, academic, or professional experience in a manufacturing or regulated environment.
• Experience or coursework related to Quality Engineering, Manufacturing Engineering, Biomedical Engineering, Mechanical Engineering, Electrical Engineering, or a related discipline.

 
Why Should You Apply?

• Health Benefits
• Referral Program
• Excellent growth and advancement opportunities