Cheiron is building AI software for regulatory lifecycle management in the pharmaceutical industry. You will be the hands-on integral regulatory affairs expert on a growing Life Sciences team, responsible for regulatory correctness across the registered life of a product, from routine maintenance to the cases the guidelines do not settle. You own the work for your assigned accounts within agreed scopes. Our Associate Director of Regulatory Affairs is the team's senior regulatory authority, and you #J-18808-Ljbffr