Life Science Jobs | Unilever is Hiring an Associate | Apply Now for Freshers Job
Looking to begin a rewarding Unilever Career in global safety and compliance? This exciting opportunity for an Associate, Global Market Vigilance (GMV) offers life science graduates a chance to work at the intersection of consumer safety, post-market surveillance, and Regulatory Affairs jobs within a world-class R&D environment. If you aspire to build impactful life science jobs in a global organization, this role is a strong career launchpad.
Job Details
- Job Title: Associate, Global Market Vigilance (GMV)
- Location: Karnataka, India
- Job ID: R-1170195
- Job Type: Full-time
- Job Category: Research & Development
- Function: Global Regulatory Affairs (GRA), Wellbeing Collective (WBC)
About the Company
Unilever is a globally recognized multinational company with a strong presence in life science jobs, consumer healthcare, and wellbeing solutions. Through its Global Regulatory Affairs division, Unilever ensures product safety, compliance, and post-market surveillance across international markets. The Unilever R&D Bangalore center plays a crucial role in supporting global safety and Regulatory Affairs jobs through data-driven vigilance systems. Known for innovation, ethics, and sustainability, Unilever offers a future-ready Unilever Career environment. The company actively supports diversity, inclusion, and continuous professional development. Working at Unilever provides exposure to global regulations, advanced safety databases, and cross-functional collaboration.
Key Responsibilities
- Support the intake, triage, and documentation of health-related complaints regarding Unilever products i.e., adverse events (AEs) using Veeva Vault Safety in an accurate and timely manner.
- Conduct duplicate checks to avoid processing redundant cases.
- Escalate AE cases to management promptly, if assessed as potentially serious in nature.
- Collaborate with internal teams (e.g., Call Centers, Customer Experience Centers) and external partners (Third-party consultants) to gather complete information regarding AE cases.
- Assist in the preparation of AE case narratives, causality assessments, and regulatory submissions under supervision, as required.
- Ensure compliance with global AE reporting requirements and timelines.
- Maintain accurate records and support documentation archiving processes.
- Assist in the configuration, user testing, and validation of safety database updates and enhancements.
- Coordinate with cross-functional teams (e.g., Regulatory Affairs, Quality Assurance, R&D) to ensure alignment of safety data and reporting.
- Track and follow up on corrective and preventive actions (CAPAs) related to safety operations.
- Support weekly and monthly reconciliations of safety data with internal and external stakeholders.
- Contribute continuous improvement ideas to enhance GMV processes and system efficiency.
- Demonstrate flexibility and readiness to take on additional activities as assigned by management.
Qualifications
- Bachelor’s or Master’s degree in Life Sciences, or a related field.
- 0-2 years of experience in post-market safety or Pharmacovigilance in Consumer Healthcare or Pharmaceutical companies.
- Hands-on experience working in scientific databases is required.
This role is an excellent opportunity for graduates aiming to enter life science jobs through a globally respected Unilever Career pathway. With exposure to safety systems, regulatory processes, and international stakeholders, this position provides a strong foundation for long-term growth in Regulatory Affairs jobs and global healthcare compliance.
