Production Supervisor, 2nd Shift

Location 245 New Park Drive,Berlin, CT, 06037,United States Employee Type FT Exempt 2nd Shift Production Supervisor Shift: 2nd Shift Status: Salaried, Exempt Schedule: 45+ hours per week as required Position Summary The 2nd Shift Production Supervisor provides hands-on technical leadership for production operations including CNC Machining, LaserTechnologies, Chemical Processing, Inspection and Assembly. This role directly supervises 40+ employees and maintains a strong floor presence, actively supporting machining, troubleshooting, scheduling, and daily execution. The supervisor is accountable for safety, quality, delivery, productivity, and cost, operating within a regulated medical device manufacturing environment requiring adherence to ISO 13485, FDA, and GMP standards. Key Responsibilities Lead daily 2nd shift production activities to meet quality, OTD, and productivity targets Provide hands‑on technical support for CNC machining, laser processing, chemical processing, inspection and assembly operations Supervise, coach, and hold accountable a large production workforce (40+ direct reports) Align labor, equipment, and priorities to the production schedule Drive improvements in operator efficiency, scrap reduction, and cost Enforce safety requirements Ensure compliance with ISO 13485, FDA, and internal quality procedures Partner with Engineering, Quality, Maintenance, and Planning to resolve production issues Support continuous improvement initiatives, process changes, and new product introductions Technical Requirements Strong machining background with hands‑on knowledge of: CNC Milling, Turning, and Swiss machining Laser technology (laser tube cutting or laser‑based manufacturing processes) Close‑tolerance, medium‑to high‑volume production Complex and multi‑part fixturing. Ability to read and interpret engineering drawings, GD&T, routings, and quality documentation Qualifications Proven production supervisory or lead experience in manufacturing Experience leading large teams (30+ direct reports preferred) Medical device manufacturing experience strongly preferred Working knowledge of ISO 9001 / ISO 13485 quality systems Strong problem‑solving, communication, and decision‑making skills #J-18808-Ljbffr