Maintenance Technician Jobs

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Maintenance Technician

Life Science Outsourcing, Inc.Brea, CA
$25 - $28Onsite

About The Position

Life Science Outsourcing, Inc (LSO) is a contract manufacturer of medical devices with in-built capabilities to offer clients full-service solutions through our six divisions. Clients rely on LSO to perform all activities required to introduce their products to market, from sourcing to drop shipping. As a Maintenance Technician at our Brea, California cleanroom manufacturing site, you will be responsible for keeping equipment, HVAC and HEPA filtration systems, and facility infrastructure performing safely and in full compliance with FDA and ISO 13485 requirements. This role is ideal for someone who enjoys solving mechanical and electrical problems, takes pride in clean documentation, and wants their work to have a meaningful impact. You will manage preventive maintenance, troubleshoot issues, and contribute to facility projects, seeing the direct connection between your work and the products shipped.

Requirements

  • High school diploma or GED required.
  • Minimum 3 years of hands-on maintenance experience in a manufacturing environment.
  • Demonstrated experience with preventive maintenance programs and CMMS software.
  • Practical knowledge of HVAC/HEPA filtration, pneumatics, and electrical and mechanical troubleshooting.
  • Ability to read and interpret technical manuals, P&IDs, electrical schematics, and maintenance procedures.
  • Working knowledge of Cal/OSHA regulations, LOTO procedures, and safe chemical handling.

Nice To Haves

  • A technical or vocational degree or certificate in industrial maintenance, mechatronics, HVAC, or a related field is preferred.
  • Medical device, pharmaceutical, or other FDA-regulated experience is strongly preferred.
  • Cleanroom maintenance experience in ISO Class 7 or 8 environments.
  • Calibration coordination experience in a regulated manufacturing setting.
  • Certifications in electrical, HVAC, or industrial maintenance.

Responsibilities

  • Execute scheduled PM tasks on cleanroom production equipment, HVAC/HEPA filtration, compressed air systems, and utilities, following written SOPs and PM work orders.
  • Document all PM activity in the eQMS, recording findings, parts used, and corrective actions.
  • Monitor and record cleanroom environmental parameters (temperature, humidity, differential pressure) and escalate deviations per procedure.
  • Inspect and replace HEPA filters, pre-filters, and related air-handling components on validated schedules.
  • Diagnose and repair mechanical, electrical, and equipment failures with minimal downtime to production.
  • Troubleshoot PLCs, motor controls, conveyors, sealing equipment, and general manufacturing machinery.
  • Escalate complex failures to senior maintenance staff or outside vendors, with accurate fault and repair documentation.
  • Respond to emergency maintenance requests during and outside scheduled shift hours as business needs require.
  • Perform general facility work including plumbing, painting, carpentry, lighting, and interior repairs.
  • Support calibration activities by coordinating with Quality and external calibration vendors so equipment stays tracked and available.
  • Assist with installation and qualification of new equipment, including IQ/OQ/PQ protocols as directed.
  • Maintain proper storage and security of tools, spare parts, and hazardous materials per SDS and site safety policy.
  • Follow all cleanroom gowning, behavior, and contamination-control protocols in ISO-classified areas.
  • Ensure maintenance activities comply with cGMPs, FDA 21 CFR Part 820, and ISO 13485 requirements.
  • Participate in non-conformance investigations, CAPA processes, and internal or external audits as requested.
  • Complete work orders, maintenance logs, and deviation reports accurately to support traceability and audit readiness.
  • Adhere to all Cal/OSHA Title 8 regulations and LSO safety policies, including lockout/tagout, arc flash, confined space, and chemical safety.
  • Promptly report unsafe conditions, near-misses, and injuries, and participate in safety investigations.
  • Maintain current training certifications for all assigned safety programs.

Benefits

  • Your work directly supports the manufacture of life-saving medical devices.
  • Hands-on variety: production equipment, building systems, and facility projects, not the same task every day.
  • Regulated-industry experience (FDA, ISO 13485) that strengthens your career.
  • A team that treats safety, quality, and precision as non-negotiable standards.

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