need 5 years of RA experience in the dossier compilation of registered medicines. The position could suit you will be managing the RA team, rather than compiling dossiers. Although you may need to jump in every dossier compilations. BPharm degree required. 5 years of RA experience in dossier compilation and new
need 5 years of RA experience in the dossier compilation of registered medicines. The position could suit you will be managing the RA team, rather than compiling dossiers. Although you may need to jump in every dossier compilations. BPharm degree required. 5 years of RA experience in dossier compilation and new
Regulatory Affairs Department Key Job Outputs: Compilation and update of documents to be submitted to regulatory regulatory authorities, this includes the compilation of Common Technical Documents (CTDs) in accordance relevant guidelines and regional requirements Compilation, update and/ or amendment of internal document Ensuring that annual product quality reviews are compiled according to cGMP standards and adverse trends relating to the testing and manufacturing process Compilation and /or update of manufacturing and cleaning
Regulatory Affairs Department Key Job Outputs: Compilation and update of documents to be submitted to regulatory regulatory authorities, this includes the compilation of Common Technical Documents (CTDs) in accordance relevant guidelines and regional requirements Compilation, update and/ or amendment of internal document Ensuring that annual product quality reviews are compiled according to cGMP standards and adverse trends relating to the testing and manufacturing process Compilation and /or update of manufacturing and cleaning
Regulatory Affairs Department Key Job Outputs: Compilation and/ or update of manufacturing and cleaning according to relevant regulatory guidelines Compilation of process qualification protocols and reports Ensuring that annual product quality reviews are compiled according to cGMP standards and adverse trends relating to the testing and manufacturing process Compilation and update of documents to be submitted to regulatory regulatory authorities, this includes compilation of common technical documents Ensuring that related
Regulatory Affairs Department Key Job Outputs: Compilation and/ or update of manufacturing and cleaning according to relevant regulatory guidelines Compilation of process qualification protocols and reports Ensuring that annual product quality reviews are compiled according to cGMP standards and adverse trends relating to the testing and manufacturing process Compilation and update of documents to be submitted to regulatory regulatory authorities, this includes compilation of common technical documents Ensuring that related
Perform bank reconciliations. Compile and review income statements. Compile monthly files including income sheet reconciliations. Review overhead expenses. Compile cash flow forecasts. Prepare finance reports. Maintain Assist in budget preparation. Prepare audit files, compile and review reconciliations. Assist auditors with
Financial Controller to join their team in Pretoria to compile and provide accurate and timeous Financial information reports and returns Prepare general ledger journals Compile general ledger reconciliations Prepare and plan variance report of Actuals to budgeted information Compile daily stock holding report Oversee Stock Takes
duties. Preparing accounting work relating to compilations of annual financial statements. Preparation Review of financial statements in CaseWare. Compilations of Annual Financial Statements on CaseWare.
requirements of the Legal, BD and AIFA team. Compilation of reporting for the Legal, BD and AIFA team when received. Assisting in typing documents, compilation of data, formatting of documents, presentations