Production Operator Lilly Medicine Foundry at Eli Lilly and Company

Lebanon, Indiana, United States

Eli Lilly and Company Logo
Not SpecifiedCompensation
Junior (1 to 2 years)Experience Level
Full TimeJob Type
UnknownVisa
PharmaceuticalsIndustries

Requirements

  • Willingness to travel domestically and internationally to collaborate, train, and learn from other sites producing APIs
  • Expertise in assigned area (Small Molecule, Hybrid, or Biologics)
  • Ability to operate processes and equipment according to batch records, user manuals, design parameters, standard operating procedures, and work instructions
  • Understanding of Health, Safety & Environmental (HSE) requirements and ability to apply Health & Safety/Process Safety standards in GMP duties
  • Recognition of operational hazards in other area processes and ability to react appropriately
  • Capability to monitor and collect data on equipment use and performance to anticipate reliability problems
  • Adherence to compliance requirements (safety, quality, and environmental) and ability to communicate/troubleshoot adverse events
  • Following cGMP practices, safe work habits, plant dress code, and hygiene standards

Responsibilities

  • Actively support start-up activities to bring manufacturing equipment into service and educate the team on proper facility operation
  • Directly oversee the production of API molecules post-project phase, ensuring a safety-first, quality-always approach
  • Adhere to compliance requirements (safety, quality, and environmental) and appropriately 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, testing, and cleaning duties to ensure equipment and systems are in good operating condition and maintained per local and corporate regulatory requirements
  • Understand HSE requirements and apply Health & Safety/Process Safety standards to execute GMP duties
  • Recognize other area processes and their operational hazards and react appropriately
  • Monitor and collect data on equipment use and performance to anticipate potential reliability problems
  • Contact 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 at handover
  • Participate in daily shift huddles/meetings to understand and set expectations for daily operational goals
  • Actively participate in assigned building and area operations such as safety audits, procedure coordination, housekeeping, and continuous improvement projects
  • Support the team, follow instructions, assist with troubleshooting, collaborate cross-functionally, and uphold safety-first, quality-always mindset to ensure supply of medicines and meet production plans

Skills

GMP Operations
Manufacturing Equipment
API Production
Small Molecule
Biologics
Process Optimization
Equipment Commissioning

Eli Lilly and Company

Develops and delivers prescription medicines globally

About Eli Lilly and Company

Eli Lilly and Company is a global pharmaceutical company that focuses on discovering, developing, and delivering medicines to improve health. The company has a long history of scientific achievements, including the creation of insulin, the first life-saving treatment for diabetes. Lilly's operations involve extensive research and development to create new medications and enhance existing ones, ensuring they are safe and effective. Their products are primarily prescription medicines sold to healthcare providers for various medical conditions, including diabetes, cancer, and pain management. What sets Lilly apart from its competitors is its strong commitment to ethical practices and the protection of its products from counterfeiting. The company's goal is to enhance lives through innovative medical solutions while maintaining high standards of quality and ethics.

Indianapolis, IndianaHeadquarters
1876Year Founded
$1,180.1MTotal Funding
IPOCompany Stage
Biotechnology, HealthcareIndustries
10,001+Employees

Risks

Competition from Novo Nordisk's Ozempic may impact tirzepatide's market share.
Potential construction delays in Indiana could affect GLP-1 drug production timelines.
Regulatory challenges may hinder Kisunla's expansion in new Alzheimer's markets.

Differentiation

Eli Lilly's rich history includes the first life-saving insulin treatment.
Lilly's strategic partnerships enhance its position in neurodegenerative disease treatments.
FDA approval of Zepbound opens new therapeutic markets for sleep disorder treatments.

Upsides

Lilly's $9 billion complex in Indiana boosts GLP-1 drug production capacity.
Kisunla's approval in China expands Lilly's Alzheimer's treatment market in Asia.
Collaboration with EVA Pharma enhances Lilly's reputation as socially responsible.

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