Posted:1 week ago| Platform:
Work from Office
Full Time
1. Registration Requirements: Study the registration requirements in each country from time to time. Identify the data availability from database & prepare gap analysis. 2. Dossier Preparation: Prepare the dossier in prescribe format 3. Document Preparation: Understand Global Harmonization System & prepare MSDS of both Teechnical and Formulation products. Prepare other dossier related documents like Composition, Authorization letters, Specifications etc as per regulations of each country. 4. Data Scouting: Find authentic data on Chemistry, Toxicity, Ecotoxicity, Efficacy, Residues & MRLs or any other information from public domain on active ingredients and formulation. 5. Discussion: Internal discussions within regulatory team to improve knowledge and implement suggested strategies. 6. Collaboration: Interact with Marketing, Quality Control, product development, R&D & manufacturing units to collect necessary documentation like Analytics Methods, COAs, MSDS, Label, leaflet etc & samples from time to time.
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