Research Scientist / Senior Research Scientist Acute Toxicology (GLP Studies)

Why This Role Matters

Acute toxicology studies are a critical component of preclinical drug development. Before any new compound progresses to human clinical trials, its safety profile must be thoroughly evaluated under controlled laboratory conditions. The Research Scientist / Senior Research Scientist in Acute Toxicology contributes directly to regulatory safety assessment by planning, conducting, and reporting toxicology studies in compliance with GLP and international standards.
This role ensures that safety data generated supports Investigational New Drug (IND) applications and meets expectations of global regulatory authorities. By maintaining high-quality documentation, adherence to ethical standards, and scientific rigor, the position strengthens the credibility and regulatory acceptance of study outcomes.
For professionals with experience in toxicology and preclinical research, this role offers strong career progression within regulatory toxicology and drug development operations.

Job Description

Eurofins Advinus is hiring Research Scientists and Senior Research Scientists for its Acute Toxicology department in Bengaluru. The role involves planning, performing, and reporting acute toxicology studies in compliance with GLP and AAALAC guidelines.
The candidate will assist in protocol preparation, study initiation, data interpretation, and regulatory documentation. The position requires hands-on involvement in animal studies, dose formulation, biological sample collection, and coordination with Study Directors and Technical Coordinators.

Key Features of the Role

• Regulatory exposure Involvement in GLP-compliant toxicology studies
• IND support Contribution to data supporting global regulatory submissions
• Laboratory involvement Hands-on participation in acute toxicity studies
• Documentation expertise Exposure to SOP, protocol, and report preparation
• Inspection readiness Participation in GLP inspections and compliance audits
• Cross-functional collaboration Work alongside Study Directors and technical teams

Responsibilities

• Study execution Plan, perform, and report acute toxicology studies
• SOP support Assist in preparation and revision of SOPs, protocols, and reports
• Compliance participation Engage in GLP and AAALAC related activities
• Literature review Conduct scientific literature searches for study support
• Animal facility management Maintain animal house records as per GLP and AAALAC norms
• Study coordination Assist Study Director (SD) and Technical Coordinator (TC) in study planning and conduct
• Test administration Handle test item administration and dose formulation preparation
• Sample collection Perform blood collection and related procedures
• Data handling Assist in data collection, compilation, and verification
• Regulatory inspections Participate in GLP inspections and ensure compliance
• Data interpretation Support analysis and reporting of study findings
• Archiving Ensure proper archiving of study-related materials

Required Qualifications

• Education M.Sc in Zoology or Biosciences
• Specialization Toxicology
• Experience 2 to 8 years in toxicology or preclinical research
• Process knowledge Understanding of agrochemical and pharmaceutical R&D processes
• Communication Strong oral and written communication skills
• Regulatory awareness Familiarity with GLP and AAALAC standards

Educational Requirements

• Master’s degree (M.Sc) in Zoology or Biosciences
• Specialization in Toxicology preferred

Experience and Skills

• Preclinical expertise Experience in acute toxicity study conduct
• GLP knowledge Strong understanding of Good Laboratory Practices
• Technical proficiency Competence in dose preparation and biological sample handling
• Documentation skills Ability to prepare and review scientific reports
• Analytical skills Capability to interpret toxicology data
• Team collaboration Ability to work effectively with study teams
• Inspection readiness Confidence in handling regulatory audits

Salary Insights

Compensation for Research Scientist / Senior Research Scientist roles in Bengaluru varies depending on experience level (2–8 years), technical expertise, and regulatory exposure. Salary is aligned with industry standards for preclinical toxicology professionals in India.

Company Overview

Eurofins Advinus is a premier preclinical and early development Contract Research Organization (CRO) offering services in drug discovery, regulatory toxicology (safety assessment), DMPK, analytical R&D services, and API CDMO. The organization supports toxicology and early clinical studies through drug substance manufacturing and GLP-compliant research facilities.
With over 30 years of GLP compliance and certification, Eurofins Advinus has supported more than 90 end-to-end IND enabling packages submitted to global regulatory authorities including the USFDA, EMA, MHRA, and Health Canada. The organization serves biotech, pharmaceutical, biological, agrochemical, nutraceutical, and cosmetic industries.

FAQs

• Is animal handling involved? Yes, acute toxicology studies involve animal facility management and biological sample collection
• Is GLP experience mandatory? Strong understanding of GLP guidelines is required
• What industries are supported? Pharmaceutical, biotech, agrochemical, and related sectors
• Is this role inspection-facing? Yes, participation in GLP inspections is part of the role
• What growth opportunities exist? Progression into Senior Scientist, Study Director, or Regulatory Toxicology Lead roles

Application Tips

• Highlight GLP experience Clearly mention involvement in GLP-compliant studies
• Specify toxicology exposure Detail hands-on acute toxicity study experience
• Include inspection participation Mention audit or regulatory inspection exposure
• Showcase technical skills List dose formulation, sample collection, and reporting experience
• Keep resume structured Focus on scientific achievements and compliance knowledge