Jobs in East Millstone, NJ

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Facility Supervisor
Salary not disclosed
Edison, NJ 1 week ago

Biologics | Facility Maintenance Supervisor

Global 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 & Responsibilities

  • Develop 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 systems
  • Clean utilities (WFI, clean steam, compressed air, nitrogen)
  • HVAC and classified cleanroom environments
  • Process piping and automation interfaces
  • Support 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 & Qualifications

  • Bachelor’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.
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