Posted:1 month ago|
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Work from Office
Full Time
Key Responsibilities will include :
1) Experience in technical review and compilation of registration dossiers for regulated markets.
2) Review of master documents (Specifications, MFR, BMR, BPR, PVP, PVR, HTSP, HTSR, PDR, elemental impurity risk assessment, nitrosamine risk assessment, stability protocols), DMF.
3) Deficiency management for products filed to regulated markets.
 
                Medreich
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