Unilever is currently hiring for the position of Senior Associate – Global Market Vigilance (GMV) at its R&D center in Bangalore, India. This opportunity is ideal for professionals with 5–8 years of pharmacovigilance experience, particularly those skilled in safety data analytics, signal detection, adverse event management, and Veeva Vault Safety systems.
The Senior Associate GMV role is part of Unilever’s Global Regulatory Affairs (GRA) team within the Wellbeing Collective (WBC). The selected candidate will play a crucial role in post-market safety surveillance, adverse event trend analysis, and regulatory compliance for consumer wellbeing products.
Professionals with expertise in pharmacovigilance case processing, MedDRA coding, signal detection, safety dashboards, and safety database management will find this role highly relevant.
Job Details
| Parameter | Details |
|---|---|
| Position | Senior Associate – Global Market Vigilance (GMV) |
| Company | Unilever |
| Department | Global Regulatory Affairs (GRA) |
| Location | Bangalore, India |
| Employment Type | Full Time |
| Experience Required | 5–8 Years |
| Qualification | Life Sciences / Pharmacy |
| Application Deadline | 23 March 2026 |
Key Responsibilities
1. Safety Data Analytics & Signal Detection
The Senior Associate GMV will:
- Conduct global adverse event (AE) data trending and signal detection activities
- Perform quantitative and qualitative safety data analysis
- Identify safety trends, emerging risks, and unexpected product safety signals
- Develop safety dashboards, KPIs, and trend reports
- Generate predictive insights and early warning indicators
- Support signal validation and safety impact assessments
2. Pharmacovigilance Case Management
Key pharmacovigilance activities include:
- Managing adverse event intake and triage
- Processing safety cases using Veeva Vault Safety
- Conducting causality and seriousness assessments
- Ensuring compliance with global AE reporting timelines
- Performing duplicate checks and safety data quality reviews
- Applying MedDRA coding standards
3. Safety System Optimization
Responsibilities also include:
- Supporting safety database validation and configuration
- Improving data integrity and analytics readiness
- Performing safety data reconciliation and audits
- Implementing process improvements in pharmacovigilance workflows
4. Cross-Functional Collaboration
The GMV Senior Associate will collaborate with:
- Regulatory Affairs teams
- R&D departments
- Quality assurance teams
- Customer experience teams
- Global safety analytics teams
The role requires presenting safety signals, risk indicators, and safety insights to internal stakeholders.
5. Safety Reporting & Insights
- Generate safety dashboards and periodic reports
- Analyze product safety metrics
- Provide data-driven safety recommendations
- Support regulatory submissions and product safety evaluations
Qualifications
To apply for this Unilever pharmacovigilance job, candidates must meet the following criteria:
- Bachelor’s or Master’s degree in Pharmacy, Life Sciences, or related field
- 5–8 years of pharmacovigilance experience
- Experience with Veeva Vault Safety or similar PV databases
- Strong knowledge of MedDRA coding
- Familiarity with global adverse event reporting standards
- Expertise in safety analytics, dashboarding, and signal detection
Required Skills
Key competencies for this Global Market Vigilance role include:
- Pharmacovigilance case processing
- Safety data analytics
- Signal detection methodologies
- Safety database management
- Dashboarding and visualization
- Regulatory compliance knowledge
- Cross-functional stakeholder communication
Salary (Estimated)
Based on industry benchmarks for pharmacovigilance roles in Bangalore, the expected salary range for a Senior Associate GMV at Unilever is:
₹10,00,000 – ₹16,00,000 per year (CTC)
Actual compensation may vary depending on experience, skills, and internal pay structures.
Why Join Unilever?
Unilever is one of the world’s leading consumer goods companies with strong investments in product safety, regulatory science, and innovation.
Key benefits include:
- Global exposure in regulatory affairs and pharmacovigilance
- Opportunity to work with advanced safety analytics tools
- Collaborative work environment
- Career growth within global R&D and safety teams
- Strong diversity and inclusion culture
How to Apply
