Vimta Labs Ltd is seeking an experienced researcher for our Preclinical Development (PCD) team. The ideal candidate will possess 5 to 8 years of experience in conducting non-rodent toxicity studies (specifically on dogs and minipigs). This role is vital for executing safety evaluation programs that comply with national and international regulatory standards.
Role Overview
- Department: Preclinical Development (PCD)
- Company: Vimta Labs Ltd
- Location: Shamirpet, Hyderabad
- Experience: 5 to 8 years
- Role Type: Full time / Toxicology Specialist
Key Responsibilities
- Study Execution: Lead and monitor non-rodent (canine and minipig) toxicology studies.
- Protocol Development: Draft, review, and finalize study plans aligned with regulatory guidelines.
- Data Management: Collect, analyze, and interpret complex toxicological data and biological findings.
- Report Writing:
Author comprehensive study reports for submission to global regulatory agencies.
- Animal Welfare: Ensure strict adherence to IAEC, CPCSEA, and AAALAC compliance frameworks.
- GLP Compliance: Maintain absolute adherence to Good Laboratory Practice standards.
Required Qualifications
- Education: M.V.Sc (Pharmacology/Toxicology/Pathology) or Ph.D. in a relevant biological stream.
- Species Expertise: Proven hands-on experience handling, dosing, and evaluating dogs and minipigs.
- Study Types: Deep knowledge of general toxicology, IND-enabling studies, and safety pharmacology.
- Soft Skills: Excellent technical writing abilities and strong project management capabilities.
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📌 Immediate opening in Toxicology Department (Hyderabad)
🏢 Vimta Labs
📍 Hyderabad