Facilities Supervisor – Biologics Manufacturing | New Jersey

About the RoleWe are supporting a commercial-stage biologics manufacturer in NJ, that has recently scaled into full GMP production following multiple FDA approvals.As part of continued site expansion, they are hiring a Facilities Supervisor to lead maintenance operations, ensure equipment reliability, and support ongoing manufacturing performance.This role is critical in maintaining GMP-compliant operations across utilities, equipment, and facility systems.Key ResponsibilitiesLead and coordinate preventative and corrective maintenance across site equipment and utilitiesManage and prioritise work through the ERP / CMMS system, assigning work orders and PMsSupport installation, upgrade, and optimisation of equipment aligned to business growthIdentify future maintenance and equipment needs to support increased production capacityOrder and manage parts for preventative maintenance, repairs, and emergency workSupport and enhance the Preventative Maintenance Program to ensure GMP complianceParticipate in investigations, CAPAs, and quality improvement initiativesEnsure all activities align with FDA and cGMP requirementsRequirementsBachelor’s degree in Mechanical, Chemical, or related Engineering field8+ years’ experience within the pharmaceutical or biopharmaceutical industry5+ years’ experience working in a cGMP environmentStrong experience managing maintenance programs, CMMS/ERP systems, and equipment reliabilityAbility to support a shift-based environment as requiredStrong communication and organisational skillsWhy ApplyJoin a growing biologics manufacturing site with approved productsPlay a key role in supporting facility performance and production uptimeExposure to GMP operations in a scaling environmentOpportunity to step into a supervisory role with real ownership