Novo Nordisk Recruitment 2026: Jr Assoc Pharmacovigilance Job in Bangalore
Novo Nordisk India has a Jr Assoc Pharmacovigilance (Junior Associate PV) opportunity in Bangalore, Karnataka. The role is associated with Regulatory Affairs & Safety and involves supporting pharmacovigilance operations, adverse event reporting, Individual Case Safety Report (ICSR) processing and drug safety documentation.
According to the supplied vacancy details, candidates with a B.Pharm degree can apply, while M.Pharm and Pharm.D are preferred qualifications. The experience range is stated as 0–2 years. Candidates interested in drug safety and pharmacovigilance can review the requirements and apply through the company’s careers portal.
Novo Nordisk Recruitment 2026 – Job Overview
| Particulars | Details |
|---|---|
| Company | Novo Nordisk India Pvt. Ltd. (Affiliate) |
| Job Title | Jr Assoc Pharmacovigilance (Junior Associate PV) |
| Requisition ID | 1455138233 |
| Department | Regulatory Affairs & Safety / Pharmacovigilance |
| Experience | 0–2 Years (as stated in the supplied vacancy details) |
| Qualification | B.Pharm |
| Preferred Qualification | M.Pharm or Pharm.D |
| Job Location | Bangalore, Karnataka, India |
| Employment Type | Full-Time, Regular / Permanent |
| Work Arrangement | On-site / Hybrid Collaborative (confirm with employer) |
| Key Systems | Veeva Safety, Veeva Quality, MedDRA |
| Application Mode | Online |
| Last Date to Apply | 20 November 2026 |
About Novo Nordisk
Novo Nordisk is a global healthcare and pharmaceutical company headquartered in Denmark. Founded in 1923, the company focuses on developing treatments for serious chronic diseases, including diabetes, obesity and rare diseases.
Its activities combine scientific research, pharmaceutical development and international healthcare operations. The supplied company information also describes its focus on patient safety, quality and regulatory compliance.
Novo Nordisk India supports international pharmaceutical operations, including regulatory affairs, pharmacovigilance and drug safety activities.
Job Description – Jr Assoc Pharmacovigilance
The Junior Associate Pharmacovigilance position supports drug safety and patient safety activities in Bangalore. The work includes receiving and documenting adverse event information, processing product quality complaints, supporting ICSR activities and maintaining regulatory safety documentation.
The role also involves coordination with Global Safety, Clinical, Regulatory and Medical teams to support accurate safety reporting and timely completion of assigned activities.
Role details:
- Position: Jr Assoc Pharmacovigilance
- Requisition ID: 1455138233
- Department: Regulatory Affairs & Safety / Pharmacovigilance
- Functional area: Pharmacovigilance, adverse event processing and safety reporting
- Experience: 0–2 years, as stated in the supplied vacancy details
- Location: Bangalore, Karnataka
Educational Qualification
Candidates should review the qualification requirements below:
- Bachelor of Pharmacy (B.Pharm) – listed qualification.
- Master of Pharmacy (M.Pharm) – preferred.
- Doctor of Pharmacy (Pharm.D) – preferred.
Training in pharmacovigilance basics can be beneficial. Knowledge of drug safety databases is also preferred.
Experience clarification: The supplied job details mention 0–2 years. The supplied FAQ further says that the published role description prefers PV training and looks for candidates with 1–2 years of relevant experience. Candidates should confirm the precise experience requirement on the official careers page.
Required Skills and Knowledge
Pharmacovigilance and Technical Skills
- Understanding of pharmacovigilance processes.
- Knowledge of adverse event reporting.
- Understanding of Individual Case Safety Report (ICSR) processing.
- Familiarity with Veeva Safety and Veeva Quality.
- Knowledge of MedDRA terminology.
- Understanding of safety documentation and case processing.
- Working knowledge of Microsoft Word, Excel and PowerPoint.
Regulatory Knowledge
Candidates should have an understanding of relevant pharmacovigilance and regulatory requirements, including:
- ICH guidelines.
- New Drugs and Clinical Trials Rules (NDCT), 2019.
- Pharmacovigilance Programme of India (PvPI).
- Good Pharmacovigilance Practices (GVP).
- Regulatory safety reporting requirements.
- Patient safety and pharmacovigilance compliance.
Professional Skills
- Good written and verbal communication.
- Strong attention to detail.
- Documentation and analytical skills.
- Ability to prioritize multiple tasks.
- Teamwork and collaboration.
- Ability to work towards regulatory reporting timelines.
- Good English communication.
- Willingness to learn pharmacovigilance systems and procedures.
Key Responsibilities
Selected candidates will support local pharmacovigilance operations and coordinate with global drug safety teams. The responsibilities listed in the supplied vacancy information include:
- Receive and document adverse event reports.
- Process product quality complaints and safety information.
- Report adverse events to Global Safety within applicable timelines.
- Monitor safety mailboxes and customer complaints.
- Perform assigned ICSR lifecycle activities.
- Prepare and review safety case narratives.
- Conduct quality checks and source data verification.
- Support clinical trial safety reporting.
- Track SUSARs, SAEs and post-marketing ICSRs.
- Maintain pharmacovigilance databases and submission trackers.
- Prepare regulatory safety documentation.
- Support audit and inspection readiness.
- Monitor local pharmacovigilance regulatory requirements.
- Escalate reporting delays and compliance issues.
- Coordinate with Clinical, Regulatory, Medical and Global Safety teams.
Benefits and Career Development
The supplied recruitment information highlights potential professional development opportunities associated with this role, including:
- Pharmacovigilance experience: Opportunity to develop knowledge of drug safety operations and case processing.
- Learning opportunities: Exposure to safety databases and pharmacovigilance procedures.
- Global exposure: Coordination with international Global Safety and cross-functional teams.
- Regulatory knowledge: Practical exposure to safety documentation and reporting requirements.
- Professional development: Development of documentation, analytical and adverse event processing skills.
- Collaborative work: Interaction with Clinical, Medical and Regulatory functions.
These are potential career and learning advantages described in the supplied information, not a guarantee of specific employee benefits. Salary, incentives, insurance and other financial benefits have not been disclosed.
How to Apply for Novo Nordisk Jobs 2026
Interested candidates can apply online through the official Novo Nordisk careers portal.
Application steps:
- Visit the official Novo Nordisk careers website.
- Search for Jr Assoc Pharmacovigilance.
- Use Requisition ID 1455138233 to locate the vacancy.
- Review the job description, qualification and experience requirements.
- Select the Apply Now option.
- Register or log in to your candidate account.
- Upload your updated resume.
- Complete the required application details.
- Review the information and submit your application.
Official careers website:
https://www.novonordisk.com/careers/find-a-job.html
Job Title: Jr Assoc Pharmacovigilance
Requisition ID: 1455138233
Location: Bangalore, Karnataka
Last Date to Apply: 20 November 2026
Applications are stated to be reviewed on an ongoing basis, so candidates are encouraged to apply early. Check the official listing for current vacancy status and final application conditions before submitting an application.
Frequently Asked Questions (FAQs)
1. What is the position available at Novo Nordisk in Bangalore?
The listed position is Jr Assoc Pharmacovigilance (Junior Associate PV), under Regulatory Affairs & Safety / Pharmacovigilance.
2. What is the required qualification?
B.Pharm is listed as the educational qualification. M.Pharm and Pharm.D are mentioned as preferred qualifications.
3. Can freshers apply for Novo Nordisk Pharmacovigilance Recruitment 2026?
The supplied vacancy details mention an experience range of 0–2 years. However, the supplied FAQ also refers to a preference for PV training and 1–2 years of relevant experience. Freshers should check the official job listing to confirm eligibility.
4. What is the job location?
The position is based in Bangalore, Karnataka, India.
5. What is the last date to apply?
The application deadline stated in the supplied recruitment details is 20 November 2026.
6. What is the requisition ID?
The requisition ID is 1455138233.
7. Which technical skills are useful for this role?
The supplied details mention pharmacovigilance processes, adverse event reporting, ICSR processing, Veeva Safety, Veeva Quality, MedDRA terminology and safety documentation.
8. How can candidates apply?
Candidates can visit the official Novo Nordisk careers portal, search for the job title or requisition ID, and submit an online application.
9. Is the salary mentioned?
No specific salary figure is provided in the supplied vacancy information.
10. Is the role on-site or hybrid?
The supplied details describe the arrangement as on-site / hybrid collaborative. Candidates should confirm the final work arrangement with the employer.
Disclaimer
This job information has been prepared from the vacancy details supplied for this post. Eligibility, experience requirements, work arrangement, application deadline and vacancy status may be subject to change. Candidates should verify all details on the official Novo Nordisk careers portal before applying. Pharma Recruiter is sharing recruitment information for candidates and is not the employer or recruitment agency for this position.
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