Research Associate – Preclinical Safety & Regulatory Support
Location: Pune (R&D), Maharashtra, India
Company: Lupin
Employment Type: Full-Time
Date Posted: February 18, 2026
ThePharmaDaily.com is featuring an opportunity for a Research Associate to join a dynamic R&D team in Pune. This role is ideal for life sciences or pharmacy graduates seeking hands-on experience in preclinical safety studies, GLP-compliant laboratory operations, and regulatory documentation support within the pharmaceutical industry.
Role Overview
The Research Associate will support regulatory documentation through scientific literature reviews and assist in the execution of in-life and terminal phases of preclinical safety studies. The position requires laboratory discipline, familiarity with GLP standards, and practical experience in animal handling and biological sample collection.
This role offers strong exposure to regulatory-aligned research environments and non-clinical development processes.
Key Responsibilities
Preclinical Study Support
Assist in the conduct of in-life and terminal phases of non-clinical safety studies.
Handle laboratory animals in compliance with ethical and regulatory guidelines.
Perform dosing and collect biological samples including blood, urine, and feces.
Ensure adherence to study protocols and experimental timelines.
Regulatory & Documentation Support
Conduct scientific literature searches to support regulatory submissions and technical write-ups.
Maintain accurate laboratory records, worksheets, raw data, and study notebooks.
Ensure documentation integrity in accordance with GLP principles and internal SOPs.
Quality & Compliance
Comply with Good Laboratory Practice (GLP) standards.
Follow written SOPs and quality procedures.
Maintain data accuracy and readiness for audits and inspections.
Experience Required
0–3 years of experience in preclinical research, toxicology studies, or laboratory-based pharmaceutical research.
Experience in animal handling, dosing techniques, and biological sample collection preferred.
Exposure to regulatory documentation or GLP environments is an advantage.
Educational Qualification
Graduation in Life Sciences or Pharmacy (mandatory).
Postgraduate degree in Life Sciences, Pharmacology, or related discipline preferred.
Core Competencies
Strong result orientation and accountability.
Customer-centric and quality-driven approach.
Good interpersonal and communication skills.
Basic understanding of regulatory guidelines and preclinical documentation requirements.
Ability to work effectively in a structured laboratory environment.
Why Apply Through ThePharmaDaily.com
This role provides foundational exposure to preclinical safety research, regulatory documentation practices, and GLP-compliant laboratory operations within a leading pharmaceutical R&D setup. It is an excellent opportunity for early-career professionals aiming to build a career in non-clinical research, toxicology, or regulatory science.
Explore more Research, Pharmacology, Preclinical, and Regulatory Affairs roles on ThePharmaDaily.com – your global platform for pharmaceutical and life sciences careers.
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