Our client in Fairfield, NJ is looking for a full time Onsite Quality Systems Manager for a direct hire position.
Responsibilities :
Responsible for implementing, establishing, auditing and maintaining the company quality system in accordance with ISO13485 / 21CFR820 and other specifications as required.
Responsible for the company’s document control system.
Responsible for the maintenance of the Master Databases on the company network used to control company documents.
Requirements :
5 years’ experience in Quality Control / Assurance in a tight tolerance industry with a medical device or life sciences customer base.
Understanding of automotive and medical industry quality requirements (APQP, FMEA, Process Flows, Control Plans, Measurement System Analysis).