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Regulatory Affairs - Executive/Assistant Manager/Deputy Manager/Manager Viatris

3.0 - 7.0 years

0 Lacs

hyderabad, telangana

On-site

As an experienced professional in the pharmaceutical industry, you will be responsible for authoring, writing, and reviewing CMC sections of dossiers. Your critical review skills will be essential in examining design stage documents such as specifications, controls, and protocols to ensure compliance with regulatory requirements. You will play a key role in assessing change controls to determine their regulatory impact and develop strategies for post-approval submissions. Coordinating the collection of post-execution data from different functions and reviewing them against design specifications will be part of your daily tasks. Collaboration with cross-functional team members will be crucial...

Posted 2 months ago

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