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Case Processing Specialist – Pharmacovigilance & Drug Safety

Abbott
Abbott
2 years
Not Disclosed
Mumbai, India
1 May 7, 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

Case Processing Specialist – Pharmacovigilance & Drug Safety Job in Mumbai, India

Company: Abbott Laboratories
Job Title: Case Processing Specialist
Location: Mumbai, India
Department: Medical and Clinical Affairs
Job Type: Full-Time


About Abbott

Abbott is a globally recognized healthcare and pharmaceutical company focused on improving lives through innovative medicines, diagnostics, medical devices, and healthcare solutions. With operations across multiple countries, Abbott continues to strengthen global patient safety and pharmacovigilance systems through advanced drug safety and clinical monitoring programs.


Job Overview

Abbott is hiring a Case Processing Specialist to support global pharmacovigilance and drug safety operations from its Mumbai office. The role is responsible for the triage, prioritization, medical coding, and end-to-end processing of Individual Case Safety Reports (ICSRs) associated with Abbott products worldwide.

The selected candidate will work on spontaneous and solicited adverse event cases, including reports received from non-interventional organized data collection schemes (NIODCS), literature sources, investigator-initiated studies, co-licensing partners, and regulatory authorities.

This position is ideal for pharmacovigilance professionals with hands-on ICSR processing experience who are looking to advance their careers in global drug safety operations.


Experience Required

Experience Level

  • Mid-Level Pharmacovigilance Professional
  • Freshers are not eligible

Required Experience

  • Minimum 2 years of practical experience in:
    • ICSR Processing
    • Pharmacovigilance
    • Drug Safety Operations

Preferred Experience

  • Safety database handling
  • Medical coding
  • Case processing for global markets
  • Literature case management
  • Adverse event reporting

Educational Qualification

Required Qualification

  • Degree in:
    • Life Sciences
    • Nursing
    • Information Management
    • Or related healthcare/scientific fields

Language Requirement

  • Good command of English communication