Regulatory Data & Authoring Analyst, Digital CMC

A global pharmaceutical company is seeking a Senior Specialist in Regulatory Authoring to oversee the optimization of regulatory processes. The role requires expertise in regulatory documentation, strong project management capabilities, and experience with digital transformation in pharmaceutical operations. Candidates must have a Bachelor's degree in a relevant field and at least five years of experience. This hybrid position involves collaboration across departments to ensure efficient execution of digital solutions and prioritization of regulatory content. #J-18808-Ljbffr