Supervisor, Facilities 3rd Shift

at  Thermo Fisher Scientific

The Facilities 3rd Shift Supervisor is responsible for supporting the new VVS commercial facility in Plainville, MA. The Facility 3rd Shift Supervisor will be the front-line contact for HVAC, process gases, steam and clean utility systems supporting GMP manufacturing, process development, quality control, and warehouse operations.

EDUCATION

• High School Diploma required and demonstrated ability in facility operations
• Bachelor’s degree preferred and proven experience in facility operations. Preference will go to those with experience in clean utilities and within a biotech/pharmaceutical environment.

EXPERIENCE

• Minimum of 5 years of relevant experience or an equivalent combination of education, industry technical training and experience.
• Direct experience supporting pharmaceutical manufacturing processes within an FDA/EMA supervised environment highly desired.
• Understanding of CMMS Systems.
• Solid understanding of Building Automation Systems and Computerized Maintenance Management System
• The candidate must have a general understanding of cGMP standards
• Solid understanding of equipment/hardware/software testing and associated protocols and lifecycle documentation requirements.

KNOWLEDGE, SKILLS, ABILITIES

• Excellent communication, technical, organizational, and interpersonal skills are essential.
• Flexibility to accommodate to rapidly changing priorities and deadlines.
• Must be a teammate prepared to lead, work in, and embrace a team-based culture
• Ability to lift 50+ lbs,
• Ability to walk, climb stairs, bend, crawl, or reach for an extended period.
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• Lead all aspects of GMP facilities night operations of a cGMP Manufacturing facility.
• Lead and develop a team to run daily facilities operations.
• Manage, prioritize, and delegate work assigned in the CMMS system for the facilities night shift team.
• Coordinate with external GMP facility cleaning team.
• Support all initiatives as identified by management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS).
• Ensure appropriate maintenance and calibration intervals for equipment and instrumentation are completed on-time.
• Set goals which align to department plans and manages the execution of goals through coaching and mentoring. Maintain a safe and professional work environment.
• Assist in the development and execution of site safety policies and procedures. Partner with EHS to champion site safety practices.
• Follows U.S. Food and Drug Administration (FDA) regulations, EMA (European Medicines Agency), other regulatory requirements, Company policies, operating procedures, processes, and task assignments. Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors