Pay Rate Low: 24 | Pay Rate High: 26
Pay Rate Low: 24 | Pay Rate High: 26

Position Overview

We are seeking an experienced Maintenance Technician to join our Facilities & Engineering team supporting sterile pharmaceutical manufacturing operations. This role is critical to ensuring equipment reliability and manufacturing continuity in a highly regulated cGMP environment.

Schedule & Location

• Shift: 5am-2pm 
• Days: Back half of week rotation (Wednesday through Friday, plus alternating Saturdays)
• Location: On-site at manufacturing facility in Thousand Oaks area

Core Responsibilities:

• Execute preventive and corrective maintenance on sterile fill-finish production equipment including filling systems, lyophilization units, and packaging machinery.
• Troubleshoot complex mechanical, electrical, and pneumatic systems to minimize unplanned downtime.
• Maintain equipment in constant audit-ready condition per federal, state, and internal quality standards.
• Prepare detailed technical documentation in accordance with current Good Manufacturing Practice (cGMP) requirements.
• Collaborate cross-functionally with Production, Engineering, and Quality teams on equipment modifications and system installations.
• Coordinate external contractors for specialized repairs and equipment upgrades.
• Identify maintenance training gaps and contribute to team capability development.
• Drive continuous improvement in maintenance procedures and equipment reliability.

Required Qualifications

Education & Experience (one of the following):

• Associate degree in Industrial Maintenance, Mechanical Technology, or related field + 2 years relevant experience, OR
• 2 years technical/trade school training with documented hands-on mechanical experience, OR
• High school diploma/GED + 4 years progressive maintenance experience

Technical Competencies:

• Demonstrated expertise in pharmaceutical or similarly regulated manufacturing equipment maintenance.
• Proficient in maintenance and repair of pumps, valves, mechanical seals, motors, and lubrication systems.
• Strong understanding of cGMP documentation requirements and predictive maintenance methodologies.
• Ability to read and interpret Piping & Instrumentation Diagrams (P&IDs), engineering drawings, and technical specifications.
• Experience with Computerized Maintenance Management Systems (CMMS).
• Comfortable working with hazardous materials, extreme temperatures, high-pressure systems, electrical voltages, and energized equipment.
• Background in pharmaceutical, biotech, or medical device manufacturing.

This job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!

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