Thermo Fisher Scientific
Indianapolis, IN
Shift: Full time
Work Schedule Second Shift (Afternoons) Environmental Conditions Able to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.) Job Description 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. Position Summary The Equipment Maintenance Technician II is a mid-level 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