Job Description: 1. Preparation of registration strategy for various health authorities of other Latin American countries i.e. Peru, Ecuador, Colombia, Panama, T&T, DMRP, Jamaica 2. Adequate understanding on respective authority guidance and filing of new product and post approval changes 3. Review of documents related to product registration and dossier submission leading to faster approval 4. Prepare response to deficiency letter received from various agencies 5. Maintain life-cycle / post approval changes for drug product registration dossiers including timely circulation of approval information 6. Provide regulatory support to cross functional department 7. Adequate assessment of change control as per regulatory guidance 8. Prepare and submit scientific advice to various health authorities Job Location: Baroda We provide equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, physical or mental disability, affectional or sexual orientation, military or veteran status, generic predisposing characteristics or any other basis prohibited by law.