Operator, Formulation (Day Shift)

Role Summary

Operator, Formulation (Day Shift) at Lilly. Supports start-up activities to bring the PAR area into service, which may include formulation, aseptic isolator barrier filling, and visual inspection. Becomes an expert in the assigned area, leading training of new staff, and, after the project phase, ensures continuous supply by running processes, troubleshooting, and collaborating cross-functionally. Opportunities for growth into future leadership and technical roles.

Responsibilities

• Provide leadership on manufacturing floor to maintain safety, quality, and productivity and ensure reliable product supply
• Maintain a safe work environment and support health, safety, and environmental goals
• Act as administrator and technical leader for operations, modeling procedures and quality systems
• Troubleshoot and escalate issues on the shop floor; serve as a primary technical resource
• Administer technical training, ensuring operators are trained to perform tasks
• Operate equipment and perform activities to meet production schedules
• Review and support execution documentation (Electronic Batch Records, SAP, Cleaning Logs)
• Drive departmental objectives including safety, deviation reduction, productivity, and training compliance
• Support site leadership to build a diverse, capable organization with robust procedures and controls
• Collaborate across operations and support functions

Qualifications

• Minimum education: High School Diploma or GED
• Effective communication (electronic, written, and verbal)
• Flexibility to troubleshoot and triage challenges
• Computer proficiency with desktop software (MS Office)
• A valid driver’s license
• Must pass a vision exam and be free of color blindness; equivalent to 20/20 close vision acuity

Education

• STEM degree or certifications (preferred)

Skills

• Leadership and ability to train/educate team members
• Aseptic filling, single-use assemblies, isolator technology
• Automated, semi-automated, and/or manual inspection
• Knowledge of CGMPs; experience in pharmaceutical, medical device, or related manufacturing
• Experience with Manufacturing Execution Systems and electronic batch release
• Continuous improvement methodologies (Lean, Six Sigma)
• Experience with highly automated equipment (inspection, packaging, filling, assembly)
• SAP and Electronic Batch Records

Additional Requirements

• Must Pass a fitness-for-duty physical exam
• Ability to work 6am to 6pm on a 2-2-3 schedule; overtime as required
• Ability to wear safety equipment and gown in a cleanroom (Grade C, ISO 8)
• Authorized to work in the United States; no visa sponsorship expected