Regulatory affairs Empleos en Grand prairie tx

A company is looking for a Senior Manager / Associate Director in Regulatory Affairs CMC.Key ResponsibilitiesContribute regulatory CMC expertise to product development and registration for small molecule investigational productsOversee the preparation and review of CMC documents for regulatory submissions, ensuring compliance and timely deliveryCollaborate with cross-functional teams and external vendors to support regulatory milestones and strategiesRequired Qualifications, Training, and EducationBS / BA degree in a scientific or health sciences discipline5+ years of experience in CMC Regulatory AffairsExperience in rare disease is a plusFamiliarity with Veeva RIM or similar document management systemsProven ability to manage timelines and processes for CMC submissions