Sr. Facilities Technician, Process Equipment

Responsibilities include execution of corrective and preventive maintenance, and operation/monitoring programs in a manner that ensures the facility is continually cGMP compliance, and sustained operation of the production and utility systems with minimal interruptions. Responsible for the maintenance and operation of the process equipment and support the clean CUP utilities. This will include the development of Maintenance documentation and materials required to support these systems. Ensure a safe work environment is maintained through adherence to environmental and health safety guidelines and policies. Support installation, repair, and troubleshooting for a wide range of Facilities and Production equipment used for all functions of a cGMP facility. Support all maintenance and repair activities within the Manufacturing Facility. Support continuous improvement and development activities of maintenance practices and procedures. Identifying and maintaining equipment spare parts inventory and replenishing spare parts as necessary to prevent significant equipment down time. Assist in support of all calibration activities as required within the Manufacturing and Development Facilities. Supervision of contractors and vendors for the performance of preventative maintenance and repairs on process equipment. As required, support 24/7 operations of the plant which may include shift coverage support as required All other duties as assigned by Facilities team 5+ years' experience in a GMP facility within biotech or pharma, or a bachelor's degree with relevant experience; alternatively, 10+ years of mechanical experience in other industries. Direct experience with performing and overseeing maintenance activities within a cGMP environment or relevant experiemce Knowledge and experience in maintenance activities supporting cGMP production preferred Knowledge and experience with clean utilities systems and processing equipment. Knowledge and experience in GDP requirements and experience documenting work within a CMMS system preferred Works on assignments that are complex in nature where considerable judgement and initiative are required in resolving problems and making recommendations. Minimum requirements are excellent writing, interpersonal and communication skills. Strong organizational skills and the ability to meet deadlines with minimal supervision. Strong understanding of clean utilities within a GMP facility. Proven ability to manage simultaneous tasks, work under pressure, track and monitor progress of multiple projects and follow through to ensure goal achievement. Capable of lifting/lowering, pushing/pulling, and carrying equipment of different dimensions and weights and utilizing equipment to assist in material handling activities. Capable of working in environments requiring use of increased personal protective equipment including chemical containment suits and respiratory protection. Ability to work within a clean room Valid Driver's license. Travel between Alnylam sites as required. Carry a mobile device and be on-call 24/7 to support manufacturing operations and emergencies