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Senior Specialist Pv Regulatory Intelligence – Pharmacovigilance

Abbott
Abbott
10+ years
Not Disclosed
Mumbai, India
1 May 8, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Environment, Experiments Design, Health And Safety (Ehs), Laboratory Equipment, Manufacturing Process, Materials Science, Process Simulation, Sop (Standard Operating Procedure), Technical Writing, Wat, GCP guidelines, gmp knowledge, HSE Knowledge , Logistics and Transportation Management, Master Data, Operational Excellence, Sap Erp, supply chain management, Supply Planning, Warehouse Management, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, mRS and EQ-5D-5L., Narrative Writing, Research & Development, Technical Skill

Senior Specialist PV Regulatory Intelligence – Pharmacovigilance Job in Mumbai, India

Company: Abbott Laboratories
Job Title: Senior Specialist PV Regulatory Intelligence
Location: Mumbai, India
Department: Research & Development / Pharmacovigilance
Industry: Pharmaceutical & Drug Safety
Job Type: Full-Time


About Abbott

Abbott is a globally recognized healthcare and pharmaceutical company committed to improving patient outcomes through innovative medicines, diagnostics, nutrition products, and medical technologies. With a strong global footprint and advanced pharmacovigilance systems, Abbott continues to lead the healthcare industry in drug safety, regulatory compliance, and clinical innovation.

The company offers professionals excellent career growth opportunities, global exposure, and a collaborative work culture focused on scientific excellence and patient safety.


Job Overview

Abbott is hiring an experienced Senior Specialist PV Regulatory Intelligence for its Pharmacovigilance and Research & Development team in Mumbai, India. This role focuses on global ICSR distribution compliance, pharmacovigilance regulatory intelligence, safety database management, and regulatory reporting activities.

The selected candidate will be responsible for ensuring accurate implementation and maintenance of global ICSR distribution rules, supporting regulatory reporting processes, monitoring pharmacovigilance regulations, and collaborating with multiple global safety and compliance teams.

This position is ideal for senior pharmacovigilance professionals with deep expertise in ICSR distribution management, global PV regulations, safety databases, and regulatory intelligence operations.


Experience Required

Experience Level

  • Senior-Level Pharmacovigilance Professional
  • Freshers are not eligible

Required Experience

  • Minimum 10 years of experience in:
    • Pharmacovigilance
    • Drug Safety Operations
    • ICSR Distribution
    • PV Regulatory Intelligence
    • Global Safety Compliance
    • Safety Database Management

Preferred Expertise

  • EMA Regulatory Reporting
  • Safety Database Configuration
  • Global PV Regulations
  • ICSR Redistribution
  • Pharmacovigilance IT Systems
  • Regulatory Rule Management

Educational Qualification

Required Qualification

Candidates must possess any of the following:

  • Master’s Degree in Science
  • Ph.D. in Life Sciences
  • B.E.
  • B.Tech
  • Equivalent qualification in a related discipline