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Careers at Lupin — Pune

Lupin is a major Indian pharma sponsor with significant Pune regulatory affairs, medical writing, and clinical operations. Strong US generics regulatory team with active ANDA filings.

Typical CTC range across roles: ₹3.8–20.0 LPA

Hiring roles

Clinical research roles Lupin hires for in Pune

Clinical research roles at Lupin in Pune

Lupin is a sponsor, and its strongest clinical-adjacent function is regulatory affairs built around US generics. The team here prepares and maintains ANDA filings, drug master files, and lifecycle submissions for the US market, with parallel work for other regulated regions. Medical writing supports these filings and the clinical documentation behind them. Pharmacovigilance runs product safety surveillance across Lupin’s marketed portfolio. There is also sponsor-side clinical operations for company studies. Because the regulatory engine is so central, a fresher who joins Lupin often sees how a submission is assembled end to end rather than working on an isolated slice.

What Lupin looks for in freshers

Pharmacy graduates such as B.Pharm and M.Pharm fit the regulatory and safety teams well, and life sciences postgraduates also apply. Regulatory candidates gain from knowing eCTD structure, the ANDA pathway, and how deficiency responses work. Safety candidates need case-processing basics and MedDRA. Writing roles want clean scientific English and the ability to summarise data faithfully. ICH-GCP and a general awareness of USFDA expectations are treated as standard for anyone entering the regulatory-heavy environment.

Interview process

Interviews tend to run technical-first. A regulatory candidate is asked about CTD modules, query timelines, and the difference between an ANDA and an NDA; a writing candidate may be given a short document task; a safety candidate walks through a narrative. A scenario round often centres on how you would handle a regulator’s query under a deadline. HR closes on notice period, relocation, and expectations.

How to prepare

Point your preparation at Lupin’s regulatory strength. Our Pharmacovigilance & Regulatory Affairs course (3 months, ₹40K + GST) covers CTD, eCTD, submission workflows, and safety case processing, while the Medical Writing course (3 months, ₹40K + GST) trains the regulatory documents its writers produce. For Lupin’s smaller pool of sponsor-side monitoring roles, the CRA career guide covers the PG Diploma route. iLearn CRI works with 50+ hiring partners across Pune’s pharma sector and offers 100% placement assistance to help freshers land a first regulatory or safety interview.

Train for Lupin — and other Pune clinical research employers

iLearn CRI's Pune-based courses prepare graduates for Lupin and Pune's broader pharma and CRO ecosystem with hands-on platform training, structured placement support, and direct hiring partner introductions.