Quality Systems Technician – ISO 9001 & CI

Kodak; City of Rochester (NY); On-site; USD 65,000 - 90,000; Full time

Job summary

Kodak in Rochester, NY seeks a Quality Technician to uphold ISO 9001:2015 QMS within the SCID team. The role emphasizes quality systems compliance, documentation control, and collaboration across scientists, engineers, production personnel, and lab technicians.

The ideal candidate has ISO 9001 and/or cGMP experience, strong organizational skills, and the ability to drive continuous improvement with cross-functional partners.

Qualifications

• Associate's or Bachelor's in a technical or scientific discipline or equivalent experience.
• Minimum 5 years of manufacturing experience.
• Strong written and verbal communication skills.
• Proficiency with Microsoft Office applications and database management systems.
• Ability to work effectively in a self-directed environment and collaborate with personnel at all organizational levels.

Responsibilities

• Maintain and support the division's ISO 9001:2015-certified Quality Management System.
• Review and control quality records and procedures.
• Collaborate with leadership to establish strategic quality objectives.
• Review material and product specifications for quality compliance.
• Track and document NCRs, investigations, CAPAs, and related quality records.
• Participate in quality investigations and root cause analysis.
• Assist with internal and external quality audits and timely resolution of findings.
• Generate and support corrective action requests (CARs).
• Prepare data, metrics, and presentations for Management Review meetings.
• Partner with cross-functional teams to identify and implement continuous improvement opportunities.

Job description

Kodak in Rochester, NY seeks a Quality Technician to uphold ISO 9001:2015 QMS within the SCID team. The role emphasizes quality systems compliance, documentation control, and collaboration across scientists, engineers, production personnel, and lab technicians.

The ideal candidate has ISO 9001 and/or cGMP experience, strong organizational skills, and the ability to drive continuous improvement with cross-functional partners.