Associate, Global Market Vigilance (GMV)

0 - 2 years

2 - 4 Lacs

Posted:10 hours ago| Platform: Naukri logo

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Job Type

Full Time

Job Description

We are 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 candi will have hands-on experience working in scientific databases and a foundational understanding of post-market safety processes in Consumer Healthcare or Pharmaceutical products.
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 up 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, Pharmacy, 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.
Key Attributes
  • Initiative-taking and collaborative team player.
  • Effective communication and documentation skills.
  • High diligence and organizational skills.
  • Ability to work in a fast-paced, cross-functional environment.

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