Facility Supervisor

Biologics | Facility Maintenance SupervisorGlobal Life Science Hub is partnered with a science-led biologics biotech that’s building a brand-new, state-of-the-art manufacturing facility in New Jersey. This site is set to become a flagship hub for commercial biologics drug substance manufacturing, with 4 cutting-edge suites scaling up to 6,000L capacity in the next 24–36 months.We are seeking a Facility Supervisor to lead and coordinate site-wide maintenance operations across facility infrastructure, clean utilities, and biologics process equipment. This role will play a critical part in establishing maintenance strategy, driving equipment reliability, and ensuring ongoing GMP readiness as the site transitions from commissioning into full commercial operations.Essential Duties & ResponsibilitiesDevelop and manage maintenance projects required to support commercial biologics manufacturing operations.Coordinate scheduled, preventative, and emergency maintenance across GMP production suites.Manage CMMS/ERP work order systems and assign maintenance activities to technicians and external contractors.Identify future equipment, resource, and spare parts requirements aligned with production scale-up plans.Order and manage parts inventory for preventative maintenance, work orders, routine servicing, and emergency repairs.Lead development and execution of a robust Preventative Maintenance Program to ensure high equipment uptime and audit readiness.Oversee maintenance and reliability of:Single-use and stainless-steel bioreactors CIP/SIP systemsClean utilities (WFI, clean steam, compressed air, nitrogen)HVAC and classified cleanroom environmentsProcess piping and automation interfacesSupport Quality Improvement initiatives including investigations, deviation response reports, and CAPA implementation related to equipment and facility systems.Ensure full compliance with FDA, cGMP, and regulatory requirements for a commercial biologics site.Requirements & QualificationsBachelor’s degree in Mechanical, Chemical, Electrical, or related Engineering discipline.Minimum 5 years supporting equipment within a cGMP-regulated environment.Strong understanding of clean utilities, facility infrastructure, and classified manufacturing environments.Ability to work across shifts based on business needs during ramp-up and commercial launch phases.Computer proficient with experience using CMMS/ERP systems.