To associate myself with a reputed pharma company where I can explore my potential effectively and work efficiently serving an organization through the phases of experiences and learning.
Preparation and evaluation of Dossiers for EU and US markets in CTD format.
鈥� Evaluation of change controls and assessing the impact on regulatory filings.
鈥� Anticipating, coordinating and resolving queries from regulatory Authorities.
鈥� Maintaining regulatory product life cycle by ensuring accurate review and submission of the concerned technical documentation in line with current effective regulation.
鈥� Coordinating with Quality Assurance, Quality Control, Formulation & Development depar...
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