This list contains only the countries for which job offers have been published in the selected language (e.g., in the French version, only job offers written in French are displayed, and in the English version, only those in English).
Facilities Maintenance Technician plays a key role in maintaining and improving the reliability, safety, and efficiency of the facility and equipment supporting sterile pharmaceutical production at the Canton, MA facility. This role requires hands-on technical skills, attention to detail, and strict adherence to cGMP (Current Good Manufacturing Practices) standards. The ideal candidate has experience in regulated manufacturing environments, a strong mechanical or electrical background, and a proactive approach to preventive and corrective maintenance.
Job Responsibility:
Repair and maintain plant equipment and building infrastructure per manufacture specifications, SOP’s incompliance with cGMP’s
Diagnose problems, replace, or repair parts, test and make appropriate adjustments
Strong understanding of electrical wiring and installation
Ensure facility and equipment are kept clean, in a safe, and serviceable condition
Interface and augment Computerized Maintenance Management System (CMMS)
Maintain spare parts inventory, order, and restock as required
Partners with Quality and follows the necessary procedures (change controls, work orders, investigation, etc.) associated with building equipment and infrastructure
Understands and monitors Building Management System (BMS) and coordination with Environmental Monitoring on temperature, relative humidity, and pressures issues
Communicates with internal departments, customers, and vendors on status of work and issues effecting services
Coordinate tasks and scheduling with vendor resources
Facilitate office and small equipment moves
Performs other related duties as assigned
Requirements:
High school diploma or equivalent
technical or trade school certification in HVAC, electrical, mechanical, or industrial maintenance preferred
3+ years of maintenance experience in a regulated manufacturing or pharmaceutical environment (503B, 503A, medical device, or biotech preferred)
Working knowledge of cGMP, FDA, and cleanroom operational standards
Demonstrated experience with maintenance management systems (CMMS)
Ability to read and interpret technical drawings, P&IDs, and equipment manuals
Strong troubleshooting skills across mechanical, electrical, pneumatic, and limited automation systems