Jobs · Management · Indiana

Production Operator Lilly Medicine Foundry

Eli Lilly and Company · Indianapolis, IN · 3 wk ago
Management$17.3–$34.38/hrFull-time

Responsibilities

  • Support the team, follow instructions, assist with troubleshooting, collaborate cross-functionally, and uphold a safety-first, quality-always mindset.
  • Adhere to compliance requirements (safety, quality, and environmental) and communicate/troubleshoot any adverse events.
  • Operate processes and equipment according to batch records, user manuals, design parameters, standard operating procedures, and work instructions to meet production schedule.
  • Perform daily monitoring, cleaning, and maintenance duties to ensure equipment and systems are in good operating condition and maintained per local and corporate regulatory requirements.
  • Understand Health, Safety & Environmental (HSE) requirements and apply Health & Safety/Process Safety standards to execute GMP duties.
  • Recognize other area processes and their operational hazards and react appropriately.
  • Maintain and collect data on equipment use and performance to anticipate potential reliability problems.
  • Contact the appropriate help if there is a problem or event (spill, deviation, incident) during manufacturing.
  • Communicate with other shifts regarding the status of area operations and any issues/problems that have occurred at handover.
  • Participate in daily shift huddles/meetings to understand and set expectations for daily operational goals.
  • Engage in assigned building and area operations such as safety audits, procedure coordination, housekeeping, and continuous improvement projects.
  • Follow cGMP practices, safe work habits, plant dress code, hygiene standards, and housekeeping requirements unique to the work area and job classification.
  • Use specified company-supplied personal protective equipment (PPE) as required.

Requirements

  • HS Diploma/GED
  • 2+ years of API manufacturing experience

Qualifications

  • Authorized to work in the United States on a full-time basis
  • A solid understanding of FDA guidelines and cGMP requirements
  • Strong organizational skills with the ability to handle and prioritize multiple requests
  • Knowledge of lean manufacturing principles
  • The ability to understand technical nomenclature and language, as well as work with mathematical formulas

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