CSA Consultant/Senior Validation Engineer 2

Required Experience & Qualifications: 5–8 years of hands-on experience supporting GxP systems in Pharmacovigilance, Clinical, Regulatory Affairs, or a combination of these domains Hands-on experience supporting GxP systems in Pharmacovigilance, Clinical, Regulatory Affairs, or a combination of these domains Strong understanding of CSA principles, CSV, and SDLC processes Experience authoring and/or reviewing validation documentation Working knowledge of GxP regulations (e.g., FDA, EMA, ICH) and …