Novo Nordisk India Urgently Opening for Pharmacovigilance Associate in Regulatory and Quality Department

Novo Nordisk India Urgently Opening for Pharmacovigilance Associate in Regulatory and Quality Department

Novo Nordisk India Urgently Opening for Pharmacovigilance Associate in Regulatory and Quality Department

Job description 

The position

  • As a Pharmacovigilance Associate, you will work on reporting customer complaints to global safety within the timelines. Handling of all the safety-related information emails received on safety mailbox.
  • You will be responsible for reporting the safety information/sever adverse events to the health authority investigators and team within the stipulated timelines and in accordance to the applicable regulations and procedures.
  • Supporting the team in archiving all the submissions made to the relevant stakeholders and acknowledgments in the study-specific files and drug product specific files.
  • You will be responsible for maintaining the electronic repository of all the submissions and acknowledgments and maintain the tracker.
  • You will manage the Periodic Safety Update Report (PSUR) notification to the health authority as per the regulations.

Qualifications

  • Below are the required skills.
  • Bachelor’s or Master’s degree in Pharmacy
  • 0-2 years of Pharmacovigilance related experience
  • Knowledge of Indian Drug Regulations
  • Highly proactive and able to take initiatives

Contact

If you have questions about the position, you are welcome to reach out to [email protected]

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