1. Preparation and compilation of CTD and ACTD dossiers for Vietnam, Myanmar and ROW market.2. Review of Process Validation, Analytical Method Validation, BMR, BPR, MFR, Stability data, COA etc. required for dossiers3. Co-ordinaing wth clients to ensure availability of documents and samples for submission.4. To develop, check & review Artworks for Labels and Pack- inserts.5. Response to queries and other requirements as required by respective regulatory authorities in a stipulated time frame.

1. Preparing Product Dossiers as per Guidelines for submission for Central America, Ghana, Kenya, Ukraine etc.2. Label artwork checking for different countries, tenders etc. as per respective guidelines.3. To prepare & update the documents like Standard Operating Procedure, Batch Manufacturing Record, Master Formula Card, Validation Protocol etc.4. To conduct & provide on job training to lab assistant as per departmental training calender.5. Formulation development of Oral Soilid, Liquid dosage forms for Domestic & ROW market as per company policy & strategy.6. Improvement in existing formulations as per company strategy.7. Carrying out Stability study as per ICH guideline for the products.8. Complete documentation during project under investigation at all steps including product development strategy, stability study etc.9. Analysis & Method development for raw materials & Finished formulation.10. Developing new approved vendors for RM, PM, CM etc.