The role involves leading the design and optimization of downstream drug substance processes for new biosynthetic candidates including peptides and oligonucleotides
Job Summary
The role involves leading the design and optimization of downstream drug substance processes for new biosynthetic candidates including peptides and oligonucleotides.
Candidates will supervise scientific staff, mentor team members, and ensure the delivery of GMP clinical material to support clinical trials and regulatory submissions.
Lilly offers a comprehensive benefit program including medical, dental, vision, prescription drug benefits, a company-sponsored 401(k), and pension plans.
Matching Summary
The role involves leading the design and optimization of downstream drug substance processes for new biosynthetic candidates including peptides and oligonucleotides.
Salary
Base: $148,500 - $257,400; Bonus/Equity: Eligible for company bonus depending on performance; Benefits: Comprehensive program including 401(k), pension, medical, dental, vision, and wellness benefits
Skills & Requirements
Must-have
Chromatography process development expertise
Peptide and oligonucleotide separation knowledge
GMP clinical material delivery experience
Process scale-up and technology transfer skills
Continuous processing and PAT implementation
Nice-to-have
Strategic thinking to overcome technical hurdles
High learning agility across multiple disciplines
Ability to interface across multiple projects
Experience with multivariate analysis
Deep understanding of global regulatory climate
Key Requirements
Ph.D. in chemical engineering, chemistry, or related field with 5+ years experience
MS Degree with 10+ years experience OR BS Degree with 12+ years experience
Experience developing purification processes from mid-development to commercialization
Experience with technical transfer into manufacturing operations