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