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| Novo Nordisk India Job Opening For Freshers & Experienced - 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 recruitment-nnipl@novonordisk.com
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