Should have core expertise & command in bioefficacy /residue data generation, knowledge of Indian agriculture, statistic design, filed trials, good relations with SAUs scientists, CIB officials. Must have sound knowledge of regulatory requirements/guidelines/ information to evaluate product as per regulatory analysis. preparing deficiency reply against queries raised by the regulatory bodies. Get the high-quality dossiers prepared, compiled, and submit in accordance with the regulatory requirements to obtain new registration as well as label extension on different crops by meeting deadlines. Coordination with internal teams for data generation on chemistry, Packaging and Toxicity, aligning with CIB& RC guidelines and compliances of labeling requirements/packaging artworks. Preparing protocols/study plans for conducting the studies. Data Gaps, Investment analysis and manage data development program for regional projects in various CROs. Be updated about recent changes in registration guidelines and interact with regulatory agencies and/or trade associations within defined area(s) of responsibility/expertise. Monitor regulatory changes, threats and opportunities to evaluate implications towards new and existing registrations. Visit to CIB, Agricultura universities, laboratories as per company demand/requirements.