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Vivanza Biosciences
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Regulatory Affairs

Regulatory Affairs

Vivanza Biosciences

3 - 7 years

|

0 Lacs

ahmedabad gujarat

Posted:4 days ago| Platform: Shine logo

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Skills Required

document preparation qa qc production coordination regulatory filing cmc review artwork coordination fd

Work Mode

On-site

Job Type

Full Time

Job Description

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.,

More Jobs at Vivanza Biosciences

Regulatory Affairs

ahmedabad, gujarat

Salary: Not disclosed

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Vivanza Biosciences

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