Abbott Hiring Pharmacovigilance Case Processing Specialist
- Abbott Hiring Case Processing Specialist in Mumbai | Pharmacovigilance & Drug Safety Role
- Company Overview
- Job Role & Responsibilities
- Key Responsibilities:
- Eligibility / Qualifications
- Educational Background:
- Experience Required:
- Skills Required:
- Location & Salary
- Application Process
- Frequently Asked Questions (FAQs)
- 1. Is this role open for freshers?
- 2. What is ICSR in pharmacovigilance?
- 3. What coding system is used in this role?
- 4. What career growth can I expect?
- Summary
Abbott Hiring Case Processing Specialist in Mumbai | Pharmacovigilance & Drug Safety Role
Looking to grow your career in pharmacovigilance and drug safety? Abbott is hiring experienced professionals for the role of Case Processing Specialist in Mumbai, India. This opportunity is ideal for candidates with at least 2 years of experience in ICSR case processing and drug safety operations. The position is part of Abbott’s Established Pharma Division and focuses on global safety data management and regulatory compliance.
This is a full-time role in the medical writing and pharmacovigilance domain, offering hands-on exposure to global adverse event reporting, safety databases, and regulatory frameworks.
Company Overview
Abbott is a globally recognized healthcare company with a strong presence in pharmaceuticals, diagnostics, medical devices, and nutrition. Known for its innovation-driven approach, Abbott operates in over 160 countries and plays a critical role in improving patient outcomes through science-based healthcare solutions.
The Established Pharma Division (EPD) focuses on delivering high-quality, trusted medicines across emerging markets, ensuring accessibility and affordability of healthcare worldwide.
Job Role & Responsibilities
As a Case Processing Specialist, you will be responsible for end-to-end pharmacovigilance case handling, ensuring compliance with global regulatory requirements and internal SOPs.
Key Responsibilities:
- Perform triage and prioritization of Individual Case Safety Reports (ICSRs) for Abbott products globally
- Handle full case processing of spontaneous and solicited ICSRs within defined timelines
- Conduct medical review and assess company causality for specific cases
- Perform MedDRA coding for adverse events, indications, and medical history
- Validate, verify, and finalize case data in safety databases
- Generate follow-up queries and manage case clarifications
- Perform case amendments, deletions, and late case investigations
- Support reconciliation, data cleanup, and database maintenance activities
- Contribute to safety database updates and data migration projects
- Maintain and update pharmacovigilance documentation such as SOPs and work instructions
Eligibility / Qualifications
Educational Background:
B.Pharmacy, M.Pharmacy, Pharm.D, BSc, MSc (Life Sciences, Nursing, Biotechnology, Microbiology, Biochemistry), Life Sciences, Healthcare, Information Management
Experience Required:
- Minimum 2 years of experience in ICSR processing or pharmacovigilance
- Experience with drug safety databases and case processing workflows
- Knowledge of global pharmacovigilance regulations and reporting timelines
- Medical coding experience using MedDRA preferred
Skills Required:
- Strong understanding of pharmacovigilance and drug safety operations
- Proficiency in Microsoft Office tools
- Good communication skills and attention to detail
- Ability to work under supervision in structured environments
Location & Salary
- Location: Mumbai, India
- Job Type: Full-time
- Salary: As per industry standards (not disclosed)
The role offers strong career growth in pharmacovigilance, regulatory affairs, and global drug safety operations, which are among the most stable and high-demand career paths in the pharmaceutical industry.
Application Process
Interested candidates can apply through the official Abbott careers portal using the link below:
Application Deadline: March 24, 2026
Candidates are advised to apply early due to limited application window.
Frequently Asked Questions (FAQs)
1. Is this role open for freshers?
No, this position requires a minimum of 2 years of experience in pharmacovigilance or ICSR processing.
2. What is ICSR in pharmacovigilance?
ICSR stands for Individual Case Safety Report, which documents adverse events related to pharmaceutical products.
3. What coding system is used in this role?
MedDRA coding is used for adverse event and medical terminology classification.
4. What career growth can I expect?
You can progress into roles such as Drug Safety Associate, Senior PV Specialist, Medical Reviewer, or Pharmacovigilance Scientist.
Summary
| Category | Details |
|---|---|
| Company | Abbott |
| Vacancies | Case Processing Specialist |
| Required Education | B.Pharmacy, M.Pharmacy, Pharm.D, BSc, MSc, Life Sciences, Nursing |
| Experience | Minimum 2 years |
To apply for this job please visit abbott.wd5.myworkdayjobs.com.
