Responsible for overall maintenance of the facility and utilities systems across the site, including preventative maintenance, work order execution, maintenance tasks, and non-routine repairs to facility and utility support systems; overall responsibility for management and supervision of supporting services required to properly maintain a state of operations readiness for manufacturing facility; oversee individuals responsible for all maintenance activities and ensure the highest quality standards and regulatory compliance are maintained; maintain long-term and weekly scheduling of facilities-related work; ensure uninterrupted operation of the facility with preventive plans for major utilities and associated systems; predict and/or correct mechanical and electrical breakdowns following strict product safety and quality standards; troubleshoot and resolve issues within a pharmaceutical manufacturing environment; manage open work orders and provide required documentation and reporting; ensure all information is tracked; serve as subject matter expert for facility and grounds maintenance expertise during customer or regulatory agency related audits; partner with Quality team to ensure processes and products are in compliance with local, state, and federal rules and regulations; ensure that processes are in cGMP compliance; and establish systems that identify opportunities to improve process effectiveness and heighten quality.
QualificationsBachelor’s degree or equivalent in Facilities Management, Facilities Engineering, or a related field and five (5) years of facility engineering or facility management experience in a pharmaceutical manufacturing environment or similar FDA-regulated environment. Alternatively, employer will accept seven (7) years of facility engineering or facility management experience in a pharmaceutical manufacturing environment or similar FDA-regulated environment. Any suitable combination of education, training, or experience is acceptable. Position also requires practical knowledge and application of cGMP, FDA, and EMA regulations; experience developing facilities and engineering management programs for a major site; experience coaching, developing, and managing a staff of employees as well as contractors; and knowledge with Microsoft Office productsundefinedundefined
HOURS: 40 hours per week (9:00 AM – 5:00 PM); Mon– Fri.
