Expertise in lc, gc, titration, and mass spectrometry
The role involves leading technical aspects of drug substance process optimization and the development of the technical agenda within a global healthcare leader
Job Summary
The role involves leading technical aspects of drug substance process optimization and the development of the technical agenda within a global healthcare leader.
Candidates must demonstrate comprehensive knowledge of Good Manufacturing Practices (GMP) and regulatory requirements while working directly in the laboratory.
This position offers the opportunity to join a strategic $1B investment hub focused on building a cutting-edge scientific organization supporting Lilly's manufacturing portfolio.
Matching Summary
The role involves leading technical aspects of drug substance process optimization and the development of the technical agenda within a global healthcare leader.
Skills & Requirements
Must-have
Ph.D. in Chemistry or Analytical Chemistry
5-12 years experience in peptide synthesis
Expertise in LC, GC, titration, and mass spectrometry
Experience with GMP and regulatory requirements
Hands-on analytical method development and transfer
Nice-to-have
Coaching and mentoring junior staff members
Embracing advanced digitization and modeling tools
Strong interpersonal skills for cross-functional teams
Proven track record of commercializing solutions
Key Requirements
Ph.D. in Chemistry or Analytical Chemistry
Post Doc preferred with focus on process chemistry
5-12 years of relevant industry experience
Experience authoring technical reports and regulatory responses