Eli Lilly and Company

Engineer - Automation

Indianapolis, Indiana, United States

Not SpecifiedCompensation
Mid-level (3 to 4 years), Senior (5 to 8 years)Experience Level
Full TimeJob Type
UnknownVisa
Healthcare, PharmaceuticalsIndustries

Company Overview

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world.

Position Overview

Engineer – Automation is responsible for establishing and maintaining the reliable operation and qualified state of the equipment/automation platforms in the area that he/she supports. The Automation Engineer engages with the cross-functional support team as an equipment/automation subject matter expert to ensure the business meets defined safety, quality, and productivity goals. The engineer also ensures that equipment/automation platforms are in-control, compliant, and capable of meeting customer needs, while delivering on projects associated with regulatory compliance, commercialization and continuous improvement efforts. This Engineer - Automation role will support the Indy Parenteral Prefilled Syringe Line.

Key Objectives/Deliverables

  • Ensure a safe working environment by following safety rules and helping improve the safety culture.
  • Take overall responsibility for the safe design and safe operation of the equipment within the area.
  • Function as automation subject matter expert of platforms of responsible equipment/system.
  • Follow established businesses processes and GMP procedures to deliver projects associated with regulatory compliance, commercialization and continuous improvement efforts.
  • Manage multiple projects with varying levels of complexity and business drivers.
  • Establish & monitor/trend control systems as tool for verifying and optimizing equipment performance.
  • Communicate effectively with others, especially process team members, operations, engineering tech, and crafts personnel.
  • Perform impact assessments of varying levels of changes to responsible equipment/systems.
  • Advise and coach other engineers and cross-functional teams, particularly in engineering best practices and automation-related topics.
  • Evaluate activities for impact to qualified state of equipment.
  • Responsible for system/component classification and maintenance strategy for equipment.
  • Implement corrections, corrective actions, and countermeasures arising from Regulatory audits and/or CAPA plans.
  • Lead or participate in IQ/OQ/PQ activities (including commissioning activities of new equipment or areas).
  • Understand equipment reliability issues with the objective of improvement.
  • Coordinate with site/corporate asset management personnel to replicate improvements and assure alignment of maintenance and other equipment activities.
  • Identify and drive improvement opportunities associated with equipment within the area.
  • Lead troubleshooting efforts to resolve more difficult equipment and operational problems.
  • Utilize formal problem-solving techniques, including Root Cause Analysis, to resolve equipment issues.
  • Engage with original equipment manufacturers and other service vendors to build knowledge base and deliver on projects and troubleshooting efforts.

Basic Requirements

  • Bachelors Degree in Electrical Engineering, Mechanical Engineering or equivalent.

Additional Preferences

  • Demonstrated ability to work in a safe manner to ensure the safety of self and others.
  • Knowledge and experience of GMP manufacturing environment.
  • Experience with designing, developing, qualifying and troubleshooting automated machines.
  • Demonstrated competency with automation/controls platforms such as Rockwell and Allen Bradley.
  • Adequate interpersonal and communications skills to be able to work effectively in a cross-functional, collaborative, team-based environment.
  • Demonstrated ability to

Skills

Automation
Equipment Subject Matter Expert
GMP
Control Systems
Project Management
Safety Culture
Regulatory Compliance
Continuous Improvement

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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