Pharmacovigilance jobs at Unilever for life science graduates – GMV Associate role
Start your career in pharmacovigilance jobs with Unilever careers – GMV Associate opportunity for life science students
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Pharmacovigilance jobs at Unilever present a strong career pathway for life science job aspirants seeking global exposure. This GMV Associate role under Unilever careers focuses on adverse event reporting, post-market surveillance, and regulatory safety operations, making it an excellent entry-level pharmacovigilance opportunity in a global R&D environment.

  • Job Title: Associate, Global Market Vigilance (GMV)
  • Location: Bangalore
  • Job ID: R-1170198
  • Job Category: Research & Development
  • Function: Global Regulatory Affairs (GRA), Wellbeing Collective (WBC)

About the Company:

Unilever is a global leader in consumer healthcare, nutrition, and wellbeing products. Through its R&D and Global Regulatory Affairs teams, Unilever careers emphasize consumer safety, innovation, and compliance, offering meaningful pharmacovigilance jobs aligned with international safety standards.

Job Overview:

Unilever is looking for a meticulous and initiative-taking associate to support Global Market Vigilance (GMV) operations. This role is critical in ensuring consumer safety and regulatory compliance through effective post-market surveillance. The ideal candidate will have hands-on experience working in scientific databases and a foundational understanding of post-market safety processes in consumer healthcare or pharmaceutical products.

Educational Requirements:

  • Bachelor’s or Master’s degree in Life Sciences, Pharmacy, or related fields
  • 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.

Key Responsibilities:

  • Intake, triage, and documentation of adverse events using Veeva Vault Safety
  • Perform duplicate checks and case quality review
  • Escalate serious adverse event cases as required
  • Collaborate with internal and external stakeholders
  • Support regulatory submissions and safety reporting timelines
  • Maintain safety documentation and compliance records

Skills Required:

  • Understanding of pharmacovigilance jobs and post-market safety concepts
  • Hands-on experience with scientific or safety databases
  • Strong documentation and communication skills
  • Attention to detail and regulatory compliance mindset
  • Ability to work in cross-functional global teams

This Associate GMV role is a valuable entry point into pharmacovigilance jobs within a globally trusted organization. For candidates seeking stable, impactful life science jobs, Unilever careers provide professional growth, global exposure, and long-term learning opportunities.

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