Job Details
Regulatory Assistant will be responsible for the evaluation of product technical dossiers and preparation / customization/submission of the same to meet the requirements of the regulatory authority for registration assigned and reviewed monthly. S/he will also be responsible for the evaluation, processing and presentation of the bio-efficacy trial data for registration and market support purposes. Update/Management of regulatory database in countries of responsibility. The preparation of labels both draft and commercial as an on-going process for the new and old products as per the requirements by the regulatory authority in respective countries as assigned for the region, will also be part of the duties, among other responsibilities.
We are all about connecting with people, in a human way – showing respect, demonstrating trust, celebrating diversity. For us technology is an enabler, not the endgame. We see the value in human connectivity and how it creates new opportunities for everyone. With this, comes our promise to protect people’s safety in every way we can.
Apply via :
careers.upl-ltd.com
