Engineer - Engineering Tech Center - Parenteral Network

Eli Lilly and Company
108d$122,250 - $179,300

About The Position

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. At Lilly, we serve an extraordinary purpose. We make a difference for people around the globe by discovering, developing and delivering medicines that help them live longer, healthier, more active lives. Not only do we deliver breakthrough medications, but you also can count on us to develop creative solutions to support communities through philanthropy and volunteerism.

Requirements

  • Bachelor's degree in engineering or related technical field.
  • Minimum 5-15 plus years in cGMP manufacturing or manufacturing support experience.
  • Extensive knowledge of parenteral processing equipment and operations including formulation, filling, freeze drying, and isolation equipment.

Nice To Haves

  • Demonstrated ability to solve technical problems and implement projects.
  • Familiarity with technology advances in vial, cartridge, and syringe container closure systems.
  • Strong interpersonal and communication skills to be effective in a team based situation.
  • Ability to work across boundaries (functional, geographic, external company, etc).
  • Demonstrated learning agility.
  • Ability to work effectively with outside suppliers.

Responsibilities

  • Provide global technical expertise in the engineering sciences related to Process Engineering and secondary/tertiary loop disciplines.
  • Knowledge and stewardship of First Principles, unit operations, Equipment Flow Diagrams, Capability Calculations, Material & Energy Balances, Facilities, Root Cause applications, Equipment and Unit Operation Changes/Improvements.
  • Serve as a technical resource in Aseptic Processing and Parenteral Technologies.
  • Provide expert process engineering support globally to parenteral sites.
  • Ensure personal and team compliance with all applicable regulatory and corporate policy requirements.
  • Assist sites globally with technical evaluations, master planning, technology assessments, and specific problem resolution.
  • Provide ongoing technical support to site engineering groups, domestic and global.
  • Monitor and influence change in external codes and standards on Lilly’s behalf.
  • Provide technical consulting and leadership to Global Facilities Delivery on major capital projects.
  • Provide technical consulting and leadership to Lilly’s external manufacturing partners.
  • Investigate, develop, and integrate emerging technology and capabilities applicable to the Parenteral manufacturing process.

Benefits

  • Eligibility to participate in a company-sponsored 401(k); pension.
  • Vacation benefits.
  • Eligibility for medical, dental, vision and prescription drug benefits.
  • Flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts).
  • Life insurance and death benefits.
  • Certain time off and leave of absence benefits.
  • Well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).
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