US OSD Regulatory Submissions Lead

A leading pharmaceutical company is seeking an Executive - RA to lead regulatory submissions for Oral Solid Dosage (OSD) in the US. The candidate will ensure compliant responses to USFDA inquiries, manage post-approval submissions, and drive necessary labeling updates. With 2-3 years of relevant experience, applicants must demonstrate a solid understanding of regulatory processes and a commitment to maintaining compliance. This role emphasizes quality and accountability in the pharmaceutical lifecycle management. #J-18808-Ljbffr