Regulatory Affairs Specialist

**Regulatory Affairs Specialist**Within International Regulatory Affairs, as Regulatory professionals, we take innovative regulatory approaches to bring life-changing medicines to patients in international markets.We work across the AZ pipeline and business to accelerate Regulatory approvals for new medicines in International markets as efficiently and effectively as possible so that no patient waits.
**Accountabilities/Responsibilities**:- Document management including uploading and tracking regulatory files and systems according to established AZ procedures and regulatory requirements- Maintain documentation & records management in Veeva RIM system in accordance with defined standards & process and as requested by RAMs eg.support with Submission Ready standards/Housestyle skills & QA checks, specific authoring tasks- Input regulatory knowledge, intelligence & information into relevant systems and databases maintaining data accuracy and up to date information for the group and ...