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 and mentor scientific staff while developing control strategies to support regulatory submissions and commercialization.
Lilly offers a comprehensive benefit program including medical, dental, vision, 401(k), pension, and flexible spending accounts.
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: Company bonus depending on performance; Benefits: Comprehensive program including 401(k), pension, medical, dental, vision, life insurance, and well-being benefits
Skills & Requirements
Must-have
Chromatography process development expertise
Peptide and oligonucleotide separation knowledge
Scale-up methodologies and equipment knowledge
Technical transfer to GMP manufacturing
Continuous processing and PAT implementation
Nice-to-have
Strategic thinking to overcome technical hurdles
High learning agility across multiple disciplines
Experience with multivariate analysis
Ability to interface across multiple projects
Comfortable with scientific uncertainty
Key Requirements
Ph.D. in chemical engineering, chemistry, or related field with 5+ years experience
MS Degree with 10+ years experience OR BS with 12+ years experience
Experience developing purification processes from mid-development to commercialization
Experience with technical transfer into manufacturing operations