Looking for Pharmacovigilance jobs in India with exposure to EU regulations and global drug safety operations? Venus Remedies Limited is hiring experienced professionals for the role of Pharmacovigilance Analyst in Panchkula. Candidates with expertise in EU GVP modules, EudraVigilance, Argus Safety, signal detection, and aggregate reporting are encouraged to apply.
This Pharmacovigilance Analyst opportunity is ideal for B.Pharm, M.Pharm, Pharm.D, and Life Sciences graduates seeking growth in global pharmacovigilance operations, post-marketing surveillance, and regulatory compliance.
Job Overview
| Details | Information |
|---|---|
| Job Title | Pharmacovigilance Analyst |
| Company | Venus Remedies (VRL) |
| Experience Required | 3 โ 7 Years |
| Location | Panchkula |
| Qualification | B.Pharm, M.Pharm, Pharm.D, Life Sciences |
| Industry | Pharmacovigilance / Drug Safety |
| Employment Type | Full-Time |
Key Responsibilities
The selected Pharmacovigilance Analyst will be responsible for managing global pharmacovigilance and EU safety reporting activities, including:
- Managing and reviewing Individual Case Safety Reports (ICSRs)
- Performing case triage, MedDRA coding, WHO-DD coding, and narrative writing
- Conducting medical review and causality assessment
- Ensuring compliance with EU GVP Modules, EMA regulations, and ICH guidelines
- Supporting preparation of:
- PSUR/PBRER
- DSUR
- Signal Evaluation Reports
- Risk Management Plans (RMPs)
- Monitoring EudraVigilance submissions and regulatory timelines
- Supporting signal detection, validation, and benefit-risk evaluation
- Coordinating with Regulatory Affairs, QA, Medical Affairs, and Global Safety teams
- Maintaining Pharmacovigilance SOPs and compliance documentation
- Participating in audits, inspections, and CAPA management activities
Required Skills & Expertise
Candidates applying for this Pharmacovigilance Analyst job should have strong knowledge of:
- EU GVP Modules
- EudraVigilance reporting
- EMA Pharmacovigilance regulations
- ICH Guidelines
- Signal management and risk management
- Post-marketing surveillance
Safety Databases Experience
Hands-on experience with the following pharmacovigilance systems is preferred:
- Argus Safety
- ArisG
- Oracle Safety
Additional preferred skills include:
- MedDRA and WHO-DD coding
- E2B(R3) submissions
- Aggregate safety reporting
- Electronic safety reporting systems
- Regulatory inspection readiness
Educational Qualification
Eligible candidates must possess one of the following qualifications:
- B.Pharm
- M.Pharm
- Pharm.D
- Life Sciences Graduate
Candidates with Pharmacovigilance certifications or EU market exposure will have an added advantage.
Why Join Venus Remedies Limited?
- Opportunity to work on global pharmacovigilance projects
- Exposure to EU regulatory and safety reporting standards
- Experience with signal management and aggregate reporting
- Collaborative work environment with cross-functional global teams
- Career growth in drug safety and regulatory compliance
How to Apply
