Kailera Therapeutics, Inc. is seeking an Associate Director, Analytical Development and Quality Control to lead analytical development and QC activities for Kailera’s pipeline compounds.
The role emphasizes collaboration with cross-functional teams to ensure end-to-end drug development and GMP-compliant manufacturing timelines. The ideal candidate will have peptide chemistry expertise, regulatory filing experience (IND/NDA/MAA), and CDMO oversight, with a strong track record in NDA projects and
#J-18808-LjbffrAnalytical Development & QC Lead — Clinical & Commercial in Remote at Unknown Company
This position is listed as full time and onsite.