Thursday, 20 September 2018

Pfizer’s Walk In Interview For Assistant Manager- Regulatory Affairs - Apply Now

Pfizer’s Walk In Interview For  Assistant Manager- Regulatory Affairs - Apply Now 

Pfizer’s Need Assistant Manager- Regulatory Affairs. - Apply Now


Pfizer’s Need Assistant Manager- Regulatory Affairs.
Compilation and submission of Annual Reports (AR), including but not limited to
  • Ensuring the availability of impacted CTD sections and relevant data (for eg., stability data
  • Handling of AR change forms and review to ensure adequacy
  •  Ensuring the SPL available in DailyMed is current before Annual Report submission, if any updates made during the reporting period, the same can be requested to Drug Listing team to update SPL by providing current Labelling commodities.
Post AR submission activities
  •  Ensuring updation of 45.NDA ( as required)
  •  Replacing stability sections in PDM.
  •  Ensuring to share 356h form to the shared folder if there is any updates during compilation.
  • Resolution of issues. 
  • Remains knowledgeable about current regulations and guidance to perform day to day regulatory activities.

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