Global Regulatory CMC Director, Peptides & Oligonucleotides

Eli Lilly and Company; Indianapolis (IN); On-site; USD 148,500 - 257,400; Full time

Benefits offered by this job

Comprehensive benefits program

Company bonus eligibility

401(k) participation

Job summary

Eli Lilly and Company located in Indianapolis is seeking an experienced regulatory CMC leader to support the development of synthetic peptides and oligonucleotides. The role demands a strong understanding of global regulations, combined with technical expertise in CMC processes. Responsibilities include leading regulatory submissions and providing strategic guidance to development teams.

The ideal candidate has over 10 years of relevant experience and a degree in a science or engineering field. A comprehensive benefits program and competitive compensation are offered.

Qualifications

• 10+ years of experience in Regulatory CMC or technical CMC.
• Experience with drug development for synthetic peptides and oligonucleotides.

Responsibilities

• Lead regulatory CMC development for synthetic peptides and oligonucleotides.
• Provide regulatory guidance to development teams.

Skills

Regulatory CMC experience

Technical CMC experience

Leadership and communication skills

Collaboration skills

Education

B.S. degree in a relevant STEM field

Advanced degree preferred

Job description

Eli Lilly and Company located in Indianapolis is seeking an experienced regulatory CMC leader to support the development of synthetic peptides and oligonucleotides. The role demands a strong understanding of global regulations, combined with technical expertise in CMC processes. Responsibilities include leading regulatory submissions and providing strategic guidance to development teams.

The ideal candidate has over 10 years of relevant experience and a degree in a science or engineering field. A comprehensive benefits program and competitive compensation are offered.