JT420 - MANUFACTURING PROCESS TECHNICIAN NS

QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team. In this role, you’ll work with a highly enthusiastic team, contributing in a world-class manufacturing industry in Puerto Rico & USA.Responsibilities:Operate automated and innovative manufacturing equipment for our products' packaging operations.This individual will be trained and cross-trained to both operate and troubleshoot issues (in the event of faults and machine stops) across a variety of equipment such as: automated, assembly, labeling, printing, and robotic automationThe technician will ensure product quality by monitoring the performance of the equipment and will utilize their mechanical proficiency to conduct machine troubleshooting and problem-solving skills in a fast-paced manufacturing environment.Under limited supervision, perform equipment setup, operation, troubleshoot to meet all standards for safety, quality and efficiency.Maintain machine uptime, perform any fault clearing and clear stoppages on automated equipmentPerform basic, routine manufacturing process operations such as dispensing of raw materials, material reconciliation, line clearance, basic analytics, and record transactionsAssist in the review of documentation for assigned areas (i.e. procedures, job plans, logs, area audits and batch records)Assist as training resource on manufacturing tasks and equipment useUse human machine interfaces (HMIs) to identify alarms and correct line stoppagesEnsures components and products are available for a continuous operationCarries out equipment inspections and generates emergency, corrective, or preventative work ordersTroubleshoot and identify potential solutions for mechanical errors, safety issues or general operating inefficiencies within the production processesQualifications: Associate degree (preferred)1-3 year of experience in working experience in GMP, Medical Device, or Biotech Manufacturing regulated environmentExperience in a drug product manufacturing environment.Ability to assemble, disassemble, operate and understand simple to moderately complex equipment per proceduresAble to use computer systems to support material inventory system (SAP transactions) and electronic batch recordsSafely follow standardized operating procedures including material handling, record keeping, assembly and packaging. Must follow Good Manufacturing Practices (GMPs)Reports to Team Leader or Production Supervisor of any discrepancies to ensure quality standards and safety of operations are always maintainedTrain fellow staff on the manufacturing processes, equipment, and generalAvailable to support Operation in Non-Standard shift that includes weekends and /or holidays as determined by business skills.12 hour night shifts 6pm-6:30am