Evalueserve India has announced an exciting opportunity for experienced life sciences professionals by opening applications for the Senior Analyst โ Toxicology position in Bengaluru, Karnataka. This hybrid role is ideal for professionals with expertise in toxicology, pharmacology, regulatory toxicology, CTD dossier preparation, OECD guidelines, and Health Based Exposure Limits (HBELs).
Candidates with a Master’s degree in Pharmacy, Pharmacology, or Toxicology and 3โ5 years of relevant experience can apply for this opportunity to work with one of the world’s leading AI-enabled managed services companies serving over 30% of Fortune 500 organizations.
Job Highlights
| Particular | Details |
|---|---|
| Position | Senior Analyst โ Toxicology |
| Company | Evalueserve India |
| Job Type | Full-Time |
| Work Mode | Hybrid |
| Location | Bengaluru, Karnataka, India |
| Experience | 3โ5 Years |
| Qualification | M.Pharm / MSc Pharmacology / MSc Toxicology |
| Department | Toxicology & Regulatory Sciences |
About Evalueserve
Evalueserve is a global leader in AI-powered managed services, helping Fortune 500 companies improve business decisions through advanced analytics, research, automation, and domain expertise.
With over 4,500 professionals across 45 countries, the company has earned recognition as a Great Place to Workยฎ and ranks among the world’s leading employers for diversity and innovation.
Key Responsibilities
Selected candidates will be responsible for:
- Preparing Common Technical Document (CTD) dossiers for global regulatory submissions.
- Drafting and reviewing Health Based Exposure Limits (HBELs), including PDE, OEL, and ADI reports.
- Conducting scientific literature searches using toxicology, pharmacology, clinical, and regulatory databases.
- Evaluating toxicological data for:
- Systemic toxicity
- Genotoxicity
- Carcinogenicity
- Reproductive toxicity
- Developmental toxicity
- Skin and eye irritation
- Sensitization
- Toxicokinetics
- Preparing environmental and ecotoxicology assessments.
- Supporting pathology audits and protocol reviews.
- Ensuring compliance with GLP, OECD, ICH, EPA, IAEC, and institutional guidelines.
- Working closely with global clients and regulatory teams.
- Preparing scientific summaries and risk assessment reports.
Required Qualifications
Applicants should possess:
- Master’s Degree in Pharmacy, Pharmacology, or Toxicology.
- 3โ5 years of experience in toxicology or regulatory toxicology.
- Strong knowledge of OECD toxicology guidelines.
- Experience in CTD non-clinical module writing.
- Expertise in HBEL preparation.
- Knowledge of FDA, ICH, EPA, and EU regulatory requirements.
- Experience using toxicology and scientific literature databases.
- Excellent analytical, communication, and report-writing skills.
- Ability to manage multiple regulatory projects and client interactions.
Preferred Skills
- Regulatory Toxicology
- CTD Dossier Writing
- OECD Guidelines
- GLP Compliance
- HBEL (PDE, OEL, ADI)
- Risk Assessment
- Toxicological Data Evaluation
- Environmental Toxicology
- Ecotoxicology
- Scientific Literature Review
- Pharmacology
- Regulatory Documentation
- Client Communication
Why Join Evalueserve?
Employees can expect:
- Hybrid work flexibility
- International client exposure
- AI-driven work environment
- Career growth opportunities
- Continuous learning programs
- Collaborative global teams
- Merit-based career progression
- Inclusive workplace culture
- Opportunity to work with Fortune 500 clients
Salary
Based on current market standards for Bengaluru and similar regulatory toxicology roles:
Expected Salary: โน12,00,000 โ โน18,00,000 per annum (CTC)
Actual compensation depends on experience, interview performance, and internal compensation policies.
How to Apply
