Skip to main content
Eli Lilly and Company

Advisor / Senior Advisor - Synthetic Chemistry Process Development

6w

Eli Lilly and Company

Hyderābād, IN · Full-time · INR 2,200,000 – INR 4,200,000

About this role

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 work to discover and bring life-changing medicines to those who need them while improving the understanding and management of disease.

Lilly has made a strategic investment of more than $1B to establish a Manufacturing and Quality technical hub in Hyderabad. This hub oversees contract manufacturing of starting materials and intermediates for API manufacturing in India along with the technical services responsible for managing the scientific agenda.

The Advisor or Senior Advisor leads technical aspects of drug substance process optimization, technical transfers, and development of the technical agenda. This position requires comprehensive knowledge of the pharmaceutical industry, Good Manufacturing Practices, and regulatory requirements essential for making medicine.

The successful candidate should have a proven track record of driving technical agendas and influencing externally in the small molecule space. Join our team and make a difference in improving health for people all over the world through a culture that values excellence, integrity, and respect for people.

Requirements

  • Comprehensive knowledge of the pharmaceutical industry
  • Proven track record of driving technical agendas
  • Experience influencing externally in the small molecule space
  • Strong understanding of Good Manufacturing Practices (GMP)
  • Knowledge of regulatory requirements for drug substance processes

Responsibilities

  • Lead technical aspects of drug substance process optimization
  • Drive technical transfers and development of the technical agenda
  • Work with the team toward process development of starting materials and intermediates
  • Apply comprehensive knowledge of GMP and regulatory requirements
  • Develop the technical agenda for manufacturing and quality in the small molecule space

Benefits

  • Global culture that values excellence, integrity, and respect for people
  • Opportunity to join a company frequently ranked among the best to work for
  • Philanthropy and volunteerism programs to give back to communities