About Thermo Fisher Scientific
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
