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. Lilly is currently constructing an advanced manufacturing facility for the production of API molecules. This facility is intended to provide APIs for current and future products, including new modalities. This is a unique opportunity to be a part of the leadership team for the startup of a manufacturing site, and the successful candidate will help to build the organization, the facility and the culture to enable a successful startup into GMP manufacturing operations.

Requirements

  • Bachelor's Degree in Process, Chemical, Biochemical Engineering or related applicable STEM discipline
  • 5+ years of experience in API Manufacturing Unit Operations

Nice To Haves

  • Experience with API chemical synthesis and biotech unit operations, including chromatography
  • Understanding of GMP production environments
  • Strong technical foundation in Chemical Engineering
  • Skilled in analytical thinking and problem-solving
  • Able to work independently and collaboratively within cross-functional teams
  • Capable of coaching others to build technical expertise
  • Creative in identifying improvements and proactive in driving implementation
  • Experienced in mentoring through technical processes
  • Flexible and adaptable to meet evolving business needs

Responsibilities

  • Mentor process engineers in core engineering practices for oligonucleotide API supply
  • Promote data-driven decision-making using statistical methods and first principles
  • Support and review root cause analyses and technical documentation
  • Identify and address process knowledge gaps affecting equipment and process performance
  • Capture essential process knowledge (e.g., material/energy balances, kinetics, design basis)
  • Maintain and support process safety foundations and hazard review activities
  • Ensure equipment qualification aligns with intended use and remains valid after changes or maintenance
  • Integrate modeling and simulation to improve process understanding and control
  • Drive continuous improvement in equipment and processes as part of cross-functional teams
  • Lead or support tech transfer of new processes and unit operations
  • Guide development of user requirements, design reviews, and verification plans
  • Advise on return-to-service protocols following equipment interventions

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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