The Senior Associate Scientist I is primarily responsible for testing samples, participating in method transfer and validation activities, drafting methods, and reporting data under cGMP regulatory guidance for Large Molecules/Biologics product development and related stability studies. The position is based at Catalent’s Kansas City facility, a center for integrated development, manufacturing, and packaging of oral solid dosage forms, with modern laboratories and specialized capabilities supporting pharmaceutical development and commercial supply.
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Job Type
Full-time
Career Level
Senior