2-15 Years in Pharmaceutical industry with major experience in Global Regulatory Affairs function. Authoring and/or contributing line to CMC content for New Development & Post-approval Variations/ Supplements for Chemical Entities, Biologicals, Vaccines (INDs/ IMPDs/ NDAs/ BLAs/ ANDAs/ MAAs/) & Medical Devices (PMA/ 510(K)/ Notified bodies/ Design History File) for Global markets.
Candidates with relevant technical experience in Pharma R&D, Tech Transfer, Quality & Manufacturing, aspiring for Regulatory role can also apply, and will be considered based on fitness and potential.