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Vivanza Biosciences
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Regulatory Affairs

Regulatory Affairs

Vivanza Biosciences

2 - 6 years

|

0 Lacs

ahmedabad gujarat

Posted:6 days ago| Platform: Shine logo

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Skills Required

document preparation coa mfr pv artwork qa qc production stability data actd ctd dossiers fd cmc review regulatory filing

Work Mode

On-site

Job Type

Full Time

Job Description

**Job Description** As a candidate for the position based in Ahmedabad, you will be responsible for the following tasks: - Document preparation for COA MFR PV and stability Data. - Preparation of country specific new ACTD/CTD Dossiers. - Coordinating with artwork department. - Coordinate with F&D, QA, QC, and Production department. - CMC review of technical documentation for regulatory filing in African, LATAM, CIS Countries, and emerging markets. Please email your resume to business@vivanzabiosciences.com.,

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Vivanza Biosciences

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