Research Associate

JOB DESCRIPTION: You will be responsible for preparing and reviewing technical documents for ANDA/dossier submissions in various countries. You will need to format these documents according to CTD, ACTD, and country-specific guidelines and coordinate with other departments for any necessary technical or administrative documents. Additionally, you will be responsible for creating clear product labels and patient information leaflets, coordinating with the Drug Control Authority to obtain manufacturing licenses, and ensuring timely filing of variations and following up for approvals.