Pharm'Up 
Mankind Pharma, one of India’s leading pharmaceutical giants, is currently seeking a seasoned professional to fill the role of Study Director for Preclinical Studies at their Ambarnath (Thane) facility. This is a critical leadership role ensuring that research meets rigorous international safety and quality standards.
Job Overview
- Location: Ambarnath, Thane, Maharashtra
- Qualifications: MVSc, M Pharm, or MSc
- Experience Required: 7–10 years in GLP (Good Laboratory Practice) preclinical roles
- Application Deadline: April 20, 2026
Key Responsibilities
The Study Director acts as the single point of control for the conduct of preclinical studies. Primary duties include:
- GLP Compliance: Directing studies in strict adherence to GLP principles and GMP guidelines.
- Documentation: Drafting study plans, recording raw data, and preparing final study reports.
- SOP Management: Preparing and revising Standard Operating Procedures (SOPs) and ensuring their implementation across the test facility.
- Technical Oversight: Supervising dosing, clinical observations, necropsy, and organ collection.
- Resource Management: Handling the requisition of chemicals and reagents while ensuring lab instruments are calibrated and maintained (AMCs).
Candidate Profile
The ideal candidate should have a deep understanding of regulatory requirements and a proven track record in a laboratory environment.
- Expertise: Strong background in preclinical research and toxicology.
- Regulatory Knowledge: Proficiency in maintaining Forms B/D and MSS updates.
- Leadership: Ability to oversee technical staff and manage complex study timelines.
How to Apply
Interested candidates who meet the eligibility criteria should submit their updated CV to: Email: sandeep.pundir@bsvgroup.com
Note: Ensure you apply before the 20th of April 2026. Mention “Application for Study Director – Preclinical Studies” in the subject line for better visibility.
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