PeopleShare, Inc. is actively recruiting a Facilities Technician for a specialized manufacturing client located in Cranbury, NJ.
This is a critical, high-impact role responsible for the overall integrity and operational readiness of the facility. As a Facilities Technician, you will be the primary steward of site infrastructure, ensuring all systems meet the rigorous requirements of a regulated cGMP and FDA environment. We are seeking a technical professional who takes pride in maintaining a world-class facility where precision, safety, and operational uptime are the highest priorities.
Location: Cranbury, NJ
Employment Type: Full-Time
100% Onsite Schedule: 7:00am - 3:30pm
Pay Rate: $29-$33/hr
Key Responsibilities:
Perform preventive, predictive, and corrective maintenance on pharmaceutical manufacturing equipment and facility systems (e.g., HVAC, compressed air, purified water systems, and production equipment).
Troubleshoot and repair mechanical, electrical, pneumatic, and hydraulic systems, including PLC-controlled equipment.
Support maintenance and operation of critical utilities (HVAC, cleanrooms, air handling units, chillers, boilers, etc.) to ensure environmental control compliance.
Ensure all work is performed in accordance with cGMP, SOPs, and safety standards, including proper documentation practices.
Maintain accurate and compliant records within a Computerized Maintenance Management System (CMMS).
Assist with equipment qualifications, calibrations, and validation support activities as required in a regulated environment.
Conduct routine inspections of facility infrastructure and manufacturing equipment to proactively identify and address potential issues.
Partner closely with Manufacturing, Quality (QA/QC), and Engineering to minimize downtime and support production schedules.
Read and interpret technical drawings, P&IDs, electrical schematics, and equipment manuals.
Support audits and inspections by maintaining inspection-ready facilities and documentation.
Safely operate equipment such as scissor lifts, forklifts, and other maintenance tools.
Adhere to all EHS policies, including lockout/tagout (LOTO), confined space, and electrical safety procedures.
Qualifications:
Mandatory: Experience working within a regulated manufacturing (cGMP) environment.
3+ years of maintenance experience in a pharmaceutical, biotechnology, or regulated manufacturing setting, preferably within a contract manufacturing/CDMO setting.
Strong working knowledge of facility systems and utilities (HVAC, cleanroom environments, compressed air, water systems).
Experience troubleshooting electrical systems, PLCs, and industrial equipment.
Familiarity with cGMP documentation practices and working in an audit-ready environment.
Hands-on experience with CMMS systems for work order management and maintenance tracking.
Ability to read and interpret schematics, blueprints, and technical manuals.
Experience supporting aseptic or oral solid dose (tablets/capsules) manufacturing environments.
Knowledge of calibration, validation, and qualification processes (IQ/OQ/PQ).
HVAC certification or electrical license is a plus; Welding, fabrication, or military technical training is also highly valued.
Key Competencies:
Strong troubleshooting and root cause analysis skills.
Ability to work independently and prioritize in a fast-paced production environment.
High attention to detail with a focus on compliance and documentation accuracy.
Team-oriented with strong collaboration across cross-functional departments.
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