Cipla

Pharmacovigilance Intern at Cipla

InternshipHybridPune3 months22K/mo3 openingsWithin 30 days

About this internship

Cipla is hiring a Pharmacovigilance Intern in Pune for a 3-month, fully mentored internship. This is real, reviewed work on live projects — not a training sandbox or a certificate mill. About the internship You will join the drug safety team and work alongside people who do this professionally…

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Skills you'll use

PharmacovigilanceAdverse Event ReportingDrug SafetyMedDRARegulatory GuidelinesCase ProcessingMedical TerminologyDocumentationData Entry AccuracyICH-GCP

What you'll do

Process and document adverse event case reports.
Code events using standard medical dictionaries.
Support periodic safety report preparation.
Maintain case records to regulatory standards.
Document your work so the next person can pick it up

Who can apply

Education: pursuing or completed B.Pharm/M.Pharm/B.Sc/M.Sc in Life Sciences, Pharmacy or a related discipline
Graduation year: 2025, 2026 or 2027 batch
Minimum 60% / 6.0 CGPA (relaxable for candidates with strong practical projects)
Technical skills: working knowledge of Pharmacovigilance, Adverse Event Reporting, Drug Safety, MedDRA
Soft skills: clear written communication, ownership, willingness to document work
Experience: none required — freshers welcome; prior projects or certifications are a plus

Perks & benefits

Certificate of CompletionLetter of RecommendationPre-Placement Offer (PPO) OpportunityFlexible Working HoursMentorship from Industry ExpertsFree Learning Resources & Certification SupportReal Project & Portfolio ExposureNetworking with Professionals

Interview & selection process

1The selection process for the Pharmacovigilance Intern role at Cipla is merit-based and typically runs over 4 stages: Round 1: Application & Resume Screening — apply through this page; profiles are shortlisted on fundamentals, projects and role fit. Round 2: Online Assessment — aptitude plus role-specific questions covering Pharmacovigilance, Adverse Event Reporting, Drug Safety. Round 3: Technical / Functional Interview — a discussion of your projects and practical scenarios covering Pharmacovigilance, Adverse Event Reporting, Drug Safety, MedDRA, Regulatory Guidelines. Expect "how would you approach this?" rather than definitions. Round 4: HR Discussion — role expectations, stipend, start date, location and offer. Shortlisted candidates are contacted after applying. There are no charges at any stage of the process — Cipla never asks candidates for money.

About Cipla

About Cipla Cipla is a global pharmaceutical company headquartered in Mumbai, developing and manufacturing medicines across respiratory, HIV, oncology and other therapy areas for markets worldwide. Industry Pharmaceuticals Products and services Cipla serves customers ranging from fast-growing…

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