Quality Engineer: CMM & GMP Specialist

Zavation Medical Products; Flowood (MS); On-site; USD 65,000 - 90,000; Full time

Job summary

Zavation Medical Products is seeking a Quality Engineer to support manufacturing and quality teams, ensuring compliance with ISO and FDA standards. You will supervise quality technicians, manage calibration and gaging, and maintain shop-floor documentation while driving continuous improvement.

The role requires a technical degree or 10 years of QA experience in manufacturing, with strong attention to detail and excellent communication. On-site position with GMP adherence and regular audits.

Qualifications

• Bachelor's degree in a technical discipline or 10 years of experience in quality control/assurance in manufacturing.
• Experience programming/operating a CMM and vision style measuring systems.
• Experience supporting manufacturing and quality with ISO and FDA requirements for medical product manufacturing.

Responsibilities

• Supervise quality technicians to meet quality and regulatory requirements.
• Manage gaging calibration activities and non-conforming material handling.
• Maintain shop floor quality documents and PFMEA participation.
• Oversee CMM operation, programming, maintenance, and operator training.
• Conduct internal and external audits and ensure GMP adherence.

Skills

Quality engineering

CMM programming

Vision measuring systems

Quality documentation

Regulatory compliance

Project management

Report writing

Communication skills

Independent work

Education

Bachelor's degree in technical discipline

10 years QA experience in manufacturing

Tools

CMM software

Gage calibration

Inspection equipment upkeep

Job description

Zavation Medical Products is seeking a Quality Engineer to support manufacturing and quality teams, ensuring compliance with ISO and FDA standards. You will supervise quality technicians, manage calibration and gaging, and maintain shop-floor documentation while driving continuous improvement.

The role requires a technical degree or 10 years of QA experience in manufacturing, with strong attention to detail and excellent communication. On-site position with GMP adherence and regular audits.