Associate – Global Market Vigilance (GMV) Job at Unilever
Unilever is hiring an Associate, Global Market Vigilance (GMV) at its R&D center in Bangalore. This Associate Job role focuses on post-market safety surveillance, adverse event handling, and regulatory compliance, supporting US-based consumer healthcare businesses. It is an excellent opportunity for life science and pharmacy graduates looking to build a career in pharmacovigilance and global regulatory affairs. Graduates seeking BPharm fresher job and want to start thier career with Unilever careers can apply now.
Job Details
- Job Title: Associate, Global Market Vigilance (GMV)
- Location: Bangalore, Karnataka, India
About the Company
Unilever is a global leader in consumer goods, with a strong presence in health, hygiene, nutrition, and wellbeing products. Through its R&D and Regulatory Affairs teams, Unilever ensures product safety, scientific excellence, and compliance across global markets while embracing diversity, innovation, and sustainability.
Educational Requirements
-
Bachelor’s or Master’s degree in Pharmacy
Experience Required for Associate Job Role
- 0–2 years of experience in post-market safety, pharmacovigilance, or market vigilance
- Experience in Consumer Healthcare or Pharmaceutical companies preferred
- Hands-on experience with scientific databases is mandatory
Key Responsibilities
- Support intake, triage, and documentation of adverse events (AEs) using Veeva Vault Safety
- Performing duplicate case checks to prevent redundant processing is required for this Associate Job role
- Escalate potentially serious adverse events to management promptly
- Collaborate with Call Centers, Customer Experience teams, and third-party partners to gather complete AE information
- Assist in preparation of AE narratives, causality assessments, and regulatory submissions under supervision
- Ensure adherence to global AE reporting timelines and compliance standards
- Maintaining accurate safety records and support documentation archiving is essential for this Associate Job role
- Assist in safety database configuration, user testing, and system validation
- Coordinate with Regulatory Affairs, Quality Assurance, and R&D teams
- Track and follow up on CAPAs (Corrective and Preventive Actions)
- Support weekly and monthly safety data reconciliations
- Contribute ideas for continuous process improvement
- Demonstrate flexibility to take on additional responsibilities as required
Skills Required for Associate Job Role
- Understanding of post-market safety and pharmacovigilance processes
- Experience with Veeva Vault Safety or similar databases
- Strong documentation and data accuracy skills
- Ability to work in a fast-paced, cross-functional environment
- Excellent written and verbal communication skills
Why This Associate Job Role Is Important
- Entry-level opportunity in Global Market Vigilance / Pharmacovigilance
- Exposure to US regulatory timelines and global safety operations
- Strong foundation for careers in Drug Safety, Regulatory Affairs, and Medical Affairs
- Opportunity to work in a world-class R&D and regulatory environment
- Graduates seeking BPharm fresher job and want to start thier career with Unilever careers can apply now.
