Regulatory Affairs Specialist: SA Submissions & Compliance

Pfizer South Africa seeks a Regulatory Affairs Specialist to ensure product compliance with SAHPRA and international standards. You will prepare regulatory dossiers, liaise with SAHPRA, and guide cross‑functional teams through submissions and lifecycle management. The role supports new product launches and ongoing registrations, monitoring regulatory changes and ensuring continuous compliance within a dynamic pharmaceutical environment in Rustenburg. J-18808-Ljbffr