Regulatory Affairs

Location : Chennai

Area of Expertise : Africa , South East Asia and CIS
Job Description:
Must have through knowledge on DMF filing procedures to various regulatory authorities such as USFDA, Africa , South East Asia ,CIS etc. Should have ability to independently compile various sections of DMF such as Administrative module, QOS.

Desired Candidate Profile:
Through knowledge on DMF amendment, annual updates, variation filings procedure to the regulatory authorities as per the respective country requirement.ability to independently access change proposal from regulatory respective. DMF compilation skills.

Send your profile to pharma@internationalrecruiter.org

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