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.

1) Responsible for testing of RM/In-process, finished goods sample and other Quality control activities.perform testing and calibration activities as per the laid STP. 2) Implement the identified corrective and preventive actions. Highlight the Non-conformity observed during testing and calibration. 3) Implement guidelines for risk control and Environment safe guard. 4) Ensure good housekeeping in the laboratory. 5) Management of laboratory chemicals and gas cylinders including storage, handling and transportation. 6) Ensure adherence to sampling plan and procedures sample collection. 7) Responsible to highlight the inconsistency in samples received. 8) Responsible to maintain safe working condition and safety of equipment. 9) Maintain quality records as per the laid Management system. 10) Monitor analysis and testing performance and data analysis. 11) Ensure waste samples handling and disposal in safe manner. 12) Highlight the Non-conformity observed during testing and calibration Implement corrective and preventive actions as per the action plan. Ensure safe working environment.

Coordinating in development of label, artwork with the customer .Should have good knowledge of bottles /labels/CBB . Co-coordinating packing/raw material with the respective teams purchase/stores/production planning. Following up with the suppliers. Coordination with the customer , Development &, QC Team for packing material . Coordination with the Plant /Production team for planning. Handling the suppliers of packing materials , and ensuring the timely deliveries at plant . Internal Interactions (within the organization) Export Department , Production, Quality , Procurement & Planning , Head office also vendors. Experience of working in packaging Agro chemical industry SAP experienece required.

Process/Sub-Process Responsibilities/Activities: Must have experience in international regulatory affairs, pesticide regulatory activities in overseas countries. Registration Requirements: Study the registration requirements in each country from time to time Identify the data availability from database and prepare gap analysis Dossier Preparation: Prepare the dossiers in prescribed format Document Preparation: Understand Global Harmonization System and prepare MSDS of both Technical and Formulation products Prepare other dossier related documents like Composition, Authorization letters, Specifications, labels and leaflets etc., as per regulations of each country Data Scouting: Find authentic data on Chemistry, Toxicity, Eco toxicity, Efficacy, Residues, and MRLs or any other information from public domain on active ingredients, and formulations Discussions: Internal discussions within regulatory team to improve knowledge and implement suggested strategies. Collaboration: Interact with Marketing, Quality Control, Product Development, R&D, and Manufacturing units to collect necessary documentation like Analytical Methods, COAs, MSDS, Label, leaflet etc., and samples from time to time

Factory Manufacturing Operation Major Job Description: Day to day Communication with all factory departments Daily Plant round and update running productions lines to HO Coordinate with department to resolve the issue if line stuck Involve in weekly production planning Material ( Tech/ Bulk/ RM/ PM) follow ups from Material Management team Follow ups from online running department & warehouse for smoothly finished good release Schedule daily dispatches as per dispatch plan

Process/Sub-Process Responsibilities/Activities: Must have experience in international regulatory affairs, pesticide regulatory activities in overseas countries. Registration Requirements: Study the registration requirements in each country from time to time Identify the data availability from database and prepare gap analysis Dossier Preparation: Prepare the dossiers in prescribed format Document Preparation: Understand Global Harmonization System and prepare MSDS of both Technical and Formulation products Prepare other dossier related documents like Composition, Authorization letters, Specifications, labels and leaflets etc., as per regulations of each country Data Scouting: Find authentic data on Chemistry, Toxicity, Eco toxicity, Efficacy, Residues, and MRLs or any other information from public domain on active ingredients, and formulations Discussions: Internal discussions within regulatory team to improve knowledge and implement suggested strategies. Collaboration: Interact with Marketing, Quality Control, Product Development, R&D, and Manufacturing units to collect necessary documentation like Analytical Methods, COAs, MSDS, Label, leaflet etc., and samples from time to time