When you’re part of Thermo Fisher Scientific, you’ll do challenging work that makes a real-world impact. Our Clinical Trials Division supports the development and delivery of life-changing therapies by ensuring high-quality, compliant manufacturing and packaging operations.

Time/Shift Hours:

10-hour Shift

Monday - Thursday

2:45pm - 1:30AM

Position Summary

The Equipment Maintenance Technician III is a senior-level technical role technical role responsible for maintaining, troubleshooting, and optimizing automated manufacturing and packaging equipment in a GMP-regulated environment. This role supports equipment reliability, regulatory compliance, and operational efficiency to ensure uninterrupted production of clinical trial materials.

This position requires hands-on technical expertise, the ability to work independently on routine and moderately complex issues, and effective collaboration with cross-functional teams including Engineering, Quality, and Manufacturing.

Key Responsibilities

Equipment Maintenance & Reliability

• Perform preventive, predictive, and corrective maintenance on automated manufacturing and packaging equipment.

• Troubleshoot and repair mechanical, electrical, pneumatic, and control system issues.

• Support root cause analysis (RCA) and implement corrective and preventive actions (CAPAs).

• Ensure equipment uptime and reliability meet operational performance targets.

Technical Troubleshooting & Systems Support

• Diagnose and resolve issues involving PLC-controlled systems (Allen-Bradley, Siemens), HMIs, robotics (Fanuc preferred), and vision systems (Cognex).

• Interpret electrical schematics, mechanical drawings, and system diagrams to support troubleshooting and repairs.

• Escalate complex issues as needed while contributing to timely resolution.

Production Support

• Support equipment setup, changeovers, and line clearance activities in compliance with GMP requirements.

• Configure equipment for different products, packaging formats, and batch requirements.

• Provide real-time technical support during production to minimize downtime.

Compliance & Documentation

• Maintain accurate documentation in accordance with cGMP and Good Documentation Practices (GDP).

• Support deviation investigations, audits, and regulatory inspections.

• Follow Environmental Health & Safety (EHS) procedures, including lockout/tagout (LOTO).

Continuous Improvement

• Participate in Lean Manufacturing and continuous improvement initiatives.

• Identify opportunities to improve equipment performance, reduce downtime, and enhance product quality.

• Support Engineering in equipment upgrades, qualifications, and process improvements.

Collaboration

• Partner with Manufacturing, Quality, Engineering, and Validation teams to ensure safe and compliant operations.

• Communicate technical issues, risks, and solutions effectively.

Qualifications

Education

• Associate degree or technical certification in Mechatronics, Industrial Maintenance, Automation, or a related field, or equivalent experience.

Experience

• 2–4 years of experience in equipment maintenance within a manufacturing environment; pharmaceutical, biotech, or medical device experience preferred.

• Experience supporting automated manufacturing or packaging equipment.

Technical Skills

• Experience troubleshooting PLC systems (Allen-Bradley and/or Siemens).

• Familiarity with robotics (Fanuc preferred) and vision systems (Cognex preferred).

• Strong mechanical and electrical troubleshooting capabilities.

• Ability to read and interpret technical documentation (schematics, diagrams, manuals).

Soft Skills

• Strong problem-solving and analytical abilities.

• Ability to work independently and within a team environment.

• Effective communication skills.

• Attention to detail with a focus on quality and compliance.

Physical & Work Environment Requirements

• Ability to lift up to 50 lbs and perform physical tasks such as standing, bending, and reaching.

• Work performed in GMP-controlled environments, including cleanrooms requiring gowning.

• Flexibility to work shifts, weekends, or overtime as needed to support production.

Why Join Us?

• Work on impactful projects that support patient health worldwide

• Opportunities for career growth and technical development

• Collaborative and safety-focused work environment

• Competitive compensation and benefits package