GMP Maintenance Technician II – Biotech Equipment Expert

AGC Biologics

Bothell (WA)

On-site

USD 40,000 - 54,000

Full time

14 days+
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Job summary

AGC Biologics is seeking a Maintenance Technician II in Bothell, WA to support GMP manufacturing equipment and utility systems. You will perform preventive maintenance, assist with troubleshooting, and help ensure regulatory compliance and operational reliability.

You'll work with Manufacturing, Engineering, and Quality to maintain equipment reliability, inspection readiness, and safe facility operations in a regulated biopharma setting. Schedule: Wed–Fri, alt Sat nights 6pm–6:30am.

Qualifications

  • High school diploma or equivalent.
  • Minimum of 3 years of maintenance experience in a cGMP, FDA-regulated, or biotech environment.
  • Knowledge of maintenance procedures for manufacturing and utility systems (autoclaves, CIP/SIP, incubators, analytical equipment, process tanks).
  • Experience using Microsoft Office and GMP documentation practices.

Responsibilities

  • Perform preventive maintenance on manufacturing equipment, utility systems, and facility infrastructure.
  • Troubleshoot, install, repair, and maintain production, laboratory, and facility instrumentation.
  • Maintain equipment calibration per manufacturer requirements and site procedures.
  • Keep maintenance records, investigations, and CMMS documentation up to date.
  • Support qualification activities related to instrumentation and process improvement.
  • Escort and support vendors and contractors performing maintenance on site.

Skills

Communication skills
Customer service mindset
Analytical thinking
Independence
Safety & compliance

Education

High school diploma

Tools

Microsoft Office
Blue Mountain CMMS

Job description

AGC Biologics is seeking a Maintenance Technician II in Bothell, WA to support GMP manufacturing equipment and utility systems. You will perform preventive maintenance, assist with troubleshooting, and help ensure regulatory compliance and operational reliability.

You'll work with Manufacturing, Engineering, and Quality to maintain equipment reliability, inspection readiness, and safe facility operations in a regulated biopharma setting. Schedule: Wed–Fri, alt Sat nights 6pm–6:30am.

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