Develops and manages projects required to provide equipment required to support the business plan.
Coordinates scheduled and emergency maintenance, repair and improvements to equipment. Manages ERP work order system and assigns work orders and PM’s to staff.
Identifies future maintenance and/or equipment resources required to meet the business plan.
Orders parts for preventative maintenance, work orders, routine jobs, and emergency repairs.
Support development of the Preventative Maintenance Program to ensure that all equipment is properly maintained from a functional efficiency standpoint and in compliance with the FDA requirements to have and use a formalized equipment maintenance system.
Participates in the Quality Improvement Program by performing investigations, writing response reports, and implementing corrective actions for CAPA’s that fall within the responsibility of Production Maintenance.
Requirements
Requirements and Qualifications:
Minimum a bachelor's degree in mechanical, chemical or related engineering field.
8+ years work experiences in pharmaceutical industry.
5+ years work experiences in cGMP environment.
Must be willing to work all shifts based on business needs.
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