Quality Engineer Specialist

at  J Sterling Industries

ABOUT STERLING INDUSTRIES

Established in 1984, Sterling Industries is a North American based contract manufacturer and assembler of medical devices and sub-components. We help clients deliver successful products by providing scaled production, design-for-manufacturing expertise, supplier consolidation and other critical value chain services.
We are seeking an eager Quality Engineering Specialist to join our growing team. The role is responsible for the launch and daily management of the processes, products, equipment, people, and customers in regard to the quality management system and regulatory requirements. The role reports to the Quality Manager.

REQUIREMENTS

• Engineering bachelor’s degree, with background in quality statistics, metrology, biomedical technologies preferred.
• 3-5 years’ experience in a quality department in a medical device OEM or contract manufacturer ISO registered environment
• ISO 13485:2016 Auditor Training Certificate preferred
• High volume workload requires a conscientious attitude with accuracy and attention to detail.
• Knowledge and experience on:
• ISO 9001:2015 (ISO 13485:2016 preferred.
• Process capability and effect on processes, production, equipment, and assembly)
• Problem-solving methods (5Y, Fishbone, 8D, etc.).
• Ability to be self-managed and directed from a satellite operation

Please refer the Job description for details