Quality Coordinator - 2nd Shift - (Southington, CT)

The Quality Coordinator is responsible for ensuring in-process product quality, and compliance to existing regulations (FDA QSR: Quality System Regulation, ISO: International Standards, Divisional Policies, Divisional and Site procedures, GMP: Good Manufacturing Practices). This is a great opportunity for a quality professional with 1+ years of background in a manufacturing environment to join an established and growing medical device leader! Please note that this role is based in our Southington, CT facility and is two nd shift with core hours of 3:00 p.m.-11:00 p.m. Responsibilities/Duties: Ensure compliance to existing policies and procedures. Conduct product inspections as required (routine/special projects). Daily audits of DHR records for compliance and conformance to specifications/regulatory requirements. Generate reports on quality related data (NCs, Holds, etc.) as needed. Participate on teams working on improvements to the quality system and continuous improvement projects.