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Job Details

Manufacturing Maintenance & Calibration Engineer (339788BR)

Manufacturing and Production

Manufacturing Engineer



Millburn, New Jersey, United States

769 million. That’s how many lives are touched by Novartis products globally. And, while we’re proud of that fact, in this world of digital and technological transformation, we must ask ourselves this: how can we continue to improve and extend even more people’s lives? <br><br>Lead maintenance, calibration and continuous improvement activities for the Millburn manufacturing and major laboratory equipment, utilities and facilities to establish consistent production output while keeping down-time to a minimum and improving reliability over time.<br><br>Your responsibilities include, but are not limited to:<br><br>• Manage / perform / plan and ensure manufacturing / major laboratory equipment preventive maintenance according to plan, troubleshooting, corrective maintenance, calibration and environmental monitoring in compliance with technical standards, SOPs and applicable regulation<br>• Manage, plan and schedule compliant maintenance of utilities/facilities with third party service providers; Provide oversight and/or perform equipment and systems qualification/validation, own change controls and oversight / implementation for local projects<br>• Improve and develop manufacturing processes using statistical and empirical data; Issue/revise SOPs and protocols related to the manufacturing facility and equipment and implement global changes as required<br>• Manage procurement of spare parts and equipment in line with established processes, ensuring availability for planned maintenance and unplanned repair<br>• Provide radiation safety program support; responsible for calibration and functionality of all radiation detection equipment<br>• Evaluate, in conjunction with QA, the requirement for change control assessment/process for any equipment/facility/utility changes<br>• Support and/or perform investigations / deviations from an engineering/maintenance perspective and own timely execution of resulting CAPAs in area of responsibility; Adhere to all applicable procedures, cGMPs, company policies and any other quality or regulatory requirements. (For example: OSHA, DEA, FDA, EMEA, ANVISA, HS&E, etc.); Perform other duties as assigned<br><br><br>[#video#{#400,300#}#/video#]