Quality Engineer - GMP/ISO/CMM Expert

Zavation Medical Products, LLC; Flowood (MS); On-site; USD 70,000 - 95,000; Full time

Job summary

Zavation Medical Products, LLC in Flowood, MS is seeking a Quality Engineer to support manufacturing and quality teams, ensuring compliance with ISO and FDA requirements and GMP. This role emphasizes meticulous documentation, calibration management, and continuous improvement across the shop floor.

The position involves supervising quality technicians, managing CMM operations, handling non-conforming materials, and supporting audits and PFMEA activities while maintaining strict process controls

Qualifications

• Experience applying ISO and FDA requirements for medical manufacturing.
• Ability to communicate effectively with direct reports and management.
• Strong project management and documentation skills.
• Experience with ISO certification audits or FDA inspections.

Responsibilities

• Supervise quality technicians to meet regulatory requirements and customer needs.
• Manage gaging and calibration activities for inspection equipment.
• Handle non-conforming material on the shop floor and associated records.
• Maintain shop floor quality documents and equipment files.
• Lead or participate in PFMEA activities and internal/external audits.
• Oversee CMM operation, programming, training, and consumables.
• Conduct routine facility and equipment inspections and GMP compliance.
• Develop work instructions and procedures; ensure timely completion.

Skills

Quality technician supervision

Calibration and gaging management

Documentation control

Regulatory compliance (ISO/FDA)

Audit support

PFMEA participation

CMM operation experience

Independent work and timeline focus

Communication and report writing

Education

Bachelor's degree in a technical discipline

10 years of quality control/assurance in manufacturing

Tools

CMM

Vision style measuring systems

Job description

Zavation Medical Products, LLC in Flowood, MS is seeking a Quality Engineer to support manufacturing and quality teams, ensuring compliance with ISO and FDA requirements and GMP. This role emphasizes meticulous documentation, calibration management, and continuous improvement across the shop floor.

The position involves supervising quality technicians, managing CMM operations, handling non-conforming materials, and supporting audits and PFMEA activities while maintaining strict process controls