Visual Inspection Associate Job at Medasource in Concord
Medasource, Concord, NC, United States
Schedule: 2-2-3 rotation, 12-hour day or night shifts
Overview The Visual Inspection Associate is responsible for operating manufacturing equipment within the Visual Inspection department and supporting the cleaning and upkeep of production areas. This role requires strict adherence to procedures and compliance with current Good Manufacturing Practices (cGMPs).
Core Responsibilities Operate visual inspection production equipment in accordance with approved procedures, including: Automated Syringe Inspection Machines (ASIM)
Semi automated inspection equipment (V90+)
Robotic palletizing equipment
Follow all site procedures and work instructions to ensure compliance with cGMP standards
Respond appropriately to machine alarms in accordance with approved alarm response procedures
Accurately and contemporaneously document activities within the electronic batch record (MES) system
Gown in Controlled Not Classified (CNC) areas in accordance with site gowning requirements
Perform cleaning of CNC areas following applicable cleaning and sanitation procedures
Requirements Experience working in a manufacturing environment within a regulated industry (pharmaceutical, biotech, medical device, or similar)
Hands‑on experience operating automated or semi‑automated production equipment
Ability to follow written procedures and work instructions in compliance with cGMP standards
Comfort responding to equipment alarms and performing basic troubleshooting
Experience with or ability to accurately complete production documentation (electronic or paper)
Willingness to work 12‑hour shifts on a 2‑2‑3 rotation, including day or night shift
Ability to gown and work in Controlled Not Classified (CNC) areas and perform routine
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Overview The Visual Inspection Associate is responsible for operating manufacturing equipment within the Visual Inspection department and supporting the cleaning and upkeep of production areas. This role requires strict adherence to procedures and compliance with current Good Manufacturing Practices (cGMPs).
Core Responsibilities Operate visual inspection production equipment in accordance with approved procedures, including: Automated Syringe Inspection Machines (ASIM)
Semi automated inspection equipment (V90+)
Robotic palletizing equipment
Follow all site procedures and work instructions to ensure compliance with cGMP standards
Respond appropriately to machine alarms in accordance with approved alarm response procedures
Accurately and contemporaneously document activities within the electronic batch record (MES) system
Gown in Controlled Not Classified (CNC) areas in accordance with site gowning requirements
Perform cleaning of CNC areas following applicable cleaning and sanitation procedures
Requirements Experience working in a manufacturing environment within a regulated industry (pharmaceutical, biotech, medical device, or similar)
Hands‑on experience operating automated or semi‑automated production equipment
Ability to follow written procedures and work instructions in compliance with cGMP standards
Comfort responding to equipment alarms and performing basic troubleshooting
Experience with or ability to accurately complete production documentation (electronic or paper)
Willingness to work 12‑hour shifts on a 2‑2‑3 rotation, including day or night shift
Ability to gown and work in Controlled Not Classified (CNC) areas and perform routine
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