Quality Engineer - Medical Devices

Medical Device industry experience is must.

What You’ll Do

• 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.