Vivanza Biosciences

As a candidate for the role based in Ahmedabad with Vivanza BioSciences, your key responsibilities will include: - Document preparation for COA MFR PV and stability Data. - Preparation of country-specific new ACTD/CTD Dossiers. - Coordinating with the artwork department. - Coordinating with F&D, QA, QC, and Production departments. - CMC review of technical documentation for regulatory filing in African, LATAM, CIS Countries, and emerging markets. Please email your resume to business@vivanzabiosciences.com to apply for this position.,