Merck
A leading pharmaceutical company in Carson City seeks an Associate Principal Scientist to drive regulatory authoring processes within a digital CMC initiative. This role demands extensive knowledge of manufacturing and regulatory requirements, requiring 8+ years of relevant experience, including project management expertise. The ideal candidate will work closely with cross-functional teams to optimize data management and ensure compliance. This is a key position aimed at shaping the digitization of regulatory filing systems.
#J-18808-Ljbffr