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Carestream Health

Quality Engineer III

Rochester, NY, United States

Compensation $90,000 to $115,000 base salary per year depending on experience.

Apply on careers.carestream.com About employer

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Job details

Pay: Compensation $90,000 to $115,000 base salary per year depending on experience.
Posting language: English
Posted: Nov 10, 2026

Original job description

Images that Matter. With Teams that Matter.

Carestream is a global provider of medical imaging systems and solutions; x-ray imaging systems for non-destructive testing; and contract manufacturing.

And the work we do matters. Our products and solutions help make everyday heroes days a little easier, improve patients’ lives, and makes a difference in our communities. And it couldn’t be done without our team of hard-working, talented and caring individuals.

We are proud to have been recognized by our employees and alumni as one of America’s Best Midsize Employers and America’s Best Employers for Engineers.

Compensation $90,000 to $115,000 base salary per year depending on experience.

*This range reflects Carestream’s good faith estimate to pay fairly as starting wage. Offers will be tailored within the range based on the selected candidate’s experience, industry knowledge, technical and communication skills, and other factors that may prove relevant during the interview process, as well as geographic market differentials for the position.

Position Summary:

Must be presently located in the Rochester, NY area United States, be a US Citizen or Permanent Resident and be able to rapidly begin working at the Carestream Manufacturing facility.

No H1B sponsorships or relocation available.

Carestream Health is looking for a Manufacturing Quality Engineer to support our manufacturing operations at 1049 West Ridge Road. This position will develop, implement, and improve quality systems, process controls, inspection methods, and corrective actions. This Quality Engineer position is responsible for ensuring products and processes consistently meet customer, regulatory, safety, and quality requirements. They serve as a cross-functional leader, utilizing data analysis and structured problem-solving techniques to identify risks, eliminate defects, and improve process capability. This position ensures compliance with the organization’s Quality Management System and applicable requirements of ISO 13485, ISO 9001, the FDA Quality Management System Regulation, MDSAP, and customer-specific requirements. The position partners closely with Manufacturing, Operations, Supply Chain, Engineering, and Regulatory functions to drive product quality and operational excellence.

Position Responsibilities:

Provide hands-on quality engineering support for electromechanical assembly, testing, inspection, packaging, and service operations to ensure products and processes meet approved specifications and quality requirements.
Monitor and analyze product, process, supplier, and service quality performance using statistical methods and key metrics to identify trends, reduce defects, and improve process capability and operational performance.
Lead investigations of manufacturing defects, nonconforming material, supplier issues, service failures, and customer complaints using structured root-cause analysis, risk assessment, and corrective and preventive action methods.
Develop and maintain control plans, inspection plans, sampling methods, acceptance criteria, quality procedures, work instructions, investigation reports, and other controlled quality documentation.
Plan, review, and execute qualification, validation, measurement-system, and change-control activities for manufacturing processes, equipment, software, test methods, inspection systems, products, and materials.
Support supplier qualification and improvement, internal and external audits, quality-system compliance, employee training, and cross-functional initiatives that ensure continued conformance with applicable regulatory, customer, and company requirements.

Required Skills & Education:

Bachelor’s degree in quality, mechanical, electrical, industrial, manufacturing, biomedical, or a related engineering discipline.
4+ years of quality engineering experience (in a regulated manufacturing environment preferred).
Must be presently located in the Rochester, NY area.
Working knowledge of ISO 13485 and experience applying quality-system, documentation, risk-management, and regulatory requirements within a manufacturing environment.
Demonstrated experience investigating product and process nonconformities, leading structured root-cause analysis, and implementing sustainable corrective and preventive actions.
Experience analyzing manufacturing data and developing process controls, inspection plans, acceptance criteria, validation documentation, or other manufacturing quality records.
Strong analytical, project-management, written, and verbal communication skills.
Required in the office hybrid Monday, Wednesday and Thursday weekly.

Desired Skills:

Experience in medical-device, diagnostic-equipment, radiographic-imaging, or another FDA-regulated manufacturing environment.
Experience supporting electromechanical assembly, system-level testing, troubleshooting, returned-product analysis, installation, or service operations.
Knowledge of ISO 9001, the FDA Quality Management System Regulation, Medical Device Single Audit Program requirements, and medical-device risk-management principles.
Experience with process validation, equipment qualification, test-method validation, measurement-system analysis, statistical process control, process capability analysis, or design of experiments.
Experience with supplier qualification, supplier audits, supplier corrective actions, statistical-analysis software, enterprise resource planning systems, or electronic quality-management systems.
American Society for Quality Certified Quality Engineer, Lean Six Sigma Green Belt or Black Belt, or ISO 13485 or ISO 9001 auditor certification or training is preferred.

Work Environment:

Office

Physical Requirements:

Person must be willing and able to meet the following physical requirements:

Standing: 50-75%
Walking: 25-50%
Sitting: 1-25%
Bending: 25-50%
Carrying, Pushing or Pulling: 25-50%
Lifting 20-35 pounds: 1-25%
Lifting 35-50 pounds: 1-25%
Lifting 50-100 pounds: 0%

Carestream is an Equal Opportunity Employer

Carestream is an equal opportunity organization. We recruit, employ, train, compensate, and promote without regard to race, religion, creed, color, national origin, age, gender, sexual orientation, gender identity, marital status, disability, veteran status, or any other basis protected by applicable federal, state or local law.

Applying for a job with Carestream

All applicants must complete the on-line application process. Carestream is committed to working with and providing reasonable accommodations to individuals with disabilities. If you require assistance or an accommodation because of a disability to participate in the application process, please click accommodations

Requisition ID: 4958

Apply on careers.carestream.com About employer

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Jobs in the United States