To prepare and submit product registration dossiers of assigned products to targeted countries ROW as per CTD requirements, To respond to queries received from regulatory agencies, business unit or other stakeholders by ensuring complete and accurate information is provided within predefined timelines, to file all the required variations and renewals of assigned products in line with guidelines, to review product artwork and package inserts, Male/female (Age around 30 years)
Experience : 4 - 8 Years
No. of Openings : 02
Education : Professional Degree
Role : Regulatory Affairs Executive
Industry Type : Pharma / BioTech / Clinical Research
Gender : [ Male / Female ]
Job Country : India