V imta Labs is a leading Indian contract research and testing organization (CRO). The company supports global pharmaceutical and biopharmaceutical firms by providing comprehensive, GLP-compliant preclinical safety assessment services.
- Department: Preclinical Development (PCD)
- Designation: Team Leader / Group Leader / Deputy Manager Non-Rodent Toxicology
- Location: Shamirpet, Hyderabad
- Experience Required: 10+ Years
- Core Focus: Managing safety evaluation and toxicology studies on non-rodent test systems (specifically canines and minipigs
Key Responsibilities Study Management & Leadership
- Direct Studies: Serve as the Study Director or Principal Investigator for complex, non-rodent general toxicology, safety pharmacology, and IND-enabling studies.
- Oversee Programs: Plan, lead, and monitor end-to-end execution of non-rodent in-vivo research programs.
- Team Supervision: Guide and mentor a multi-disciplinary team of research associates, scientists, and veterinary professionals.
Protocol & Report Authoring
- Develop Protocols: Draft, review, and finalize high-quality study plans and experimental designs aligned with global standards.
- Data Interpretation:
Analyze and evaluate complex toxicological, pathology, and bio-analytical findings.
- Author Reports: Compile comprehensive, submission-ready regulatory study reports for global filings (such as the USFDA or EMA).
Compliance & Quality Assurance
- Maintain GLP: Ensure absolute compliance with Positive Laboratory Practice (GLP) rules across all testing workflows.
- Animal Welfare: Enforce strict adherence to IAEC, CPCSEA, and AAALAC compliance frameworks for animal care.
- Audit Support: Represent the non-rodent facility during internal quality assessments and external regulatory inspections.
Required Qualifications & Skills
- Education: Ph.D. or Master's degree (M.V.Sc / M.Pharm / M.Sc) in Toxicology, Pharmacology, Veterinary Science, or a related Life Sciences field.
- Expertise: Deep hands-on experience handling large animal/non-rodent biological systems (Dogs and minipigs).
- Regulatory Knowledge: Sound understanding of international guidelines (OECD, ICH, FDA) governing preclinical drug safety.
Interested candidates please share profiles to
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📌 Immediate opening For Toxicology Position ( Non-Rodent ) (Hyderabad)
🏢 Vimta Labs
📍 Hyderabad