JAMP India Pharmaceuticals has announced a new Pharmacovigilance job opening in Ahmedabad for experienced pharmacy professionals. The company is hiring for Senior Officer / Executive – Pharmacovigilance positions, offering an opportunity for candidates with experience in ICSR case processing, Argus Safety, MedDRA coding, literature review, and drug safety activities.
Candidates with a B.Pharm or M.Pharm qualification and 1–4 years of Pharmacovigilance experience are eligible to apply. The selected professionals will work on Individual Case Safety Report (ICSR) processing and other day-to-day pharmacovigilance activities while supporting the Global PV team.
JAMP India Pharmacovigilance Job Overview
| Details | Information |
|---|---|
| Company | JAMP India Pharmaceuticals |
| Department | Pharmacovigilance |
| Position | Senior Officer / Executive |
| Qualification | B.Pharm / M.Pharm |
| Experience | 1–4 Years |
| Location | Ahmedabad, Gujarat |
| Job Type | Pharmaceutical / Pharmacovigilance |
| Application Mode | |
| Posted Date | August 31, 2026 |
About the Pharmacovigilance Role
The JAMP India Pharmaceuticals Pharmacovigilance job primarily involves Individual Case Safety Report (ICSR) case processing. Professionals will review, assess, document, and process safety information according to applicable pharmacovigilance procedures and regulatory requirements.
The role also provides exposure to Argus Safety database activities, case narratives, MedDRA coding, case triage, quality review, reconciliation, aggregate safety reports, literature surveillance, and Good Pharmacovigilance Practices.
Key Responsibilities
Selected candidates for the Senior Officer / Executive Pharmacovigilance role will be responsible for:
- Perform data entry and ICSR case processing in the Argus Safety database from different safety-reporting sources.
- Track received ICSRs and enter relevant case information into the JAMP safety database.
- Manage queries associated with Individual Case Safety Reports.
- Generate concise, accurate, medically appropriate, and well-written case narratives.
- Perform consistent medical coding according to established coding conventions, including MedDRA coding.
- Conduct ICSR triage and classify reports as serious, non-serious, valid, or non-valid as applicable.
- Review pharmacovigilance cases for quality, consistency, completeness, and accuracy, including peer case reviews.
- Support reconciliation activities associated with case processing in coordination with the Global Pharmacovigilance team.
- Contribute to safety reports, including Periodic Safety Update Reports (PSURs) and Signal Detection Reports (SDRs).
- Conduct weekly literature reviews for relevant safety information.
- Perform routine day-to-day pharmacovigilance and drug safety activities.
- Review regulatory and pharmacovigilance publications to remain updated on current regulations, practices, procedures, and proposals.
- Maintain an appropriate medical understanding of relevant therapeutic areas and disease states.
- Promote and follow Good Pharmacovigilance Practices (GVP).
- Properly document relevant contacts and communications.
- Communicate effectively with managers, Global PV colleagues, and other team members and participate in required team meetings.
Qualification and Experience
Candidates interested in this Pharmacovigilance job in Ahmedabad should meet the following requirements:
Educational Qualification: B.Pharm or M.Pharm
Experience: 1–4 years of relevant professional experience, preferably in Pharmacovigilance, drug safety, ICSR case processing, or related safety operations.
Candidates with practical exposure to Argus Safety, ICSR processing, MedDRA coding, case narratives, literature review, PSURs, signal detection, and pharmacovigilance regulations may be particularly relevant to the responsibilities described in the vacancy.
Key Pharmacovigilance Skills
The role involves several core drug-safety competencies, including ICSR case processing, Oracle Argus Safety, MedDRA coding, case narrative writing, ICSR triage, case quality review, literature surveillance, PSUR preparation, signal detection, reconciliation, regulatory compliance, and Good Pharmacovigilance Practices.
Professionals who have previously worked with end-to-end safety case management and understand the regulatory importance of accurate and timely adverse-event reporting should closely match the requirements of this opportunity.
Why Consider This Opportunity?
This JAMP India Pharmaceuticals opening can provide experienced pharmacy professionals with exposure to multiple areas of pharmacovigilance rather than limiting the role to basic data entry.
The responsibilities cover ICSR processing, case quality review, global reconciliation activities, literature surveillance, aggregate safety reporting, signal detection, regulatory updates, and collaboration with a Global PV team. This can help professionals strengthen their broader drug-safety and pharmacovigilance experience.
How to Apply for JAMP India Pharmacovigilance Jobs
Eligible candidates interested in the JAMP India Pharmaceuticals Pharmacovigilance vacancy in Ahmedabad can prepare an updated CV highlighting relevant ICSR processing, Argus Safety, MedDRA, literature review, and drug-safety experience.
Application Email: dkothari@jamppharma.com