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Remote Regulatory Affairs Consultant - CMC Biologics

Parexel, Indiana, PA, United States


A leading biopharmaceutical company is seeking a Regulatory Affairs Consultant to manage lifecycle submissions for drug products. The ideal candidate will have 7-10 years of experience in regulatory affairs and a Bachelor’s degree in a relevant field. Responsibilities include preparing regulatory submissions, coordinating documentation, and staying updated on regulatory guidelines. This position supports work from home options and requires strong communication and organizational skills. #J-18808-Ljbffr