Essential Duties & Responsibilities:

• 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 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.
• Computer proficient.