Baxter has announced an exciting career opportunity for the position of Research Associate – R&D Pre-Clinical Toxicology at its Ahmedabad, Gujarat location. The company is looking for highly motivated candidates with a Master’s or PhD degree in Pharmacy, Pharmacology, Toxicology, Biotechnology, Biochemistry, Medical Sciences, Veterinary Sciences, or related disciplines.
This is a full-time opportunity for professionals who are passionate about pre-clinical toxicology, nonclinical safety assessment, toxicological risk assessment, and pharmaceutical research & development. The selected candidate will support Baxter’s Global Product Research & Development (GPRD) team in delivering scientific and regulatory toxicology projects.
Baxter Recruitment 2026 – Overview
| Particulars | Details |
|---|---|
| Company Name | Baxter |
| Job Role | Research Associate – R&D Pre-Clinical Toxicology |
| Department | Research & Development (Pre-Clinical Toxicology) |
| Job Location | Ahmedabad, Gujarat |
| Employment Type | Full-Time |
| Qualification | Master’s or PhD in Pharmacy, Science, Pharmacology, Toxicology, Biotechnology, Biochemistry, Medical Sciences, Veterinary Sciences, or Related Discipline |
| Experience | Relevant experience in Toxicology or Pre-Clinical Research preferred |
| Application Mode | Online |
| Last Date to Apply | 11 August 2026 |
Job Responsibilities
The selected candidate will be responsible for:
- Support the Pre-Clinical Toxicology team in scientific data management and integration activities.
- Conduct literature reviews and analyze scientific data for nonclinical safety assessments.
- Develop compound-specific health hazard profiles using toxicological data.
- Prepare Toxicological Risk Assessments (TRAs) for extractables, leachables, residual solvents, elemental impurities, degradation products, and related substances.
- Design, plan, monitor, and coordinate in vitro and in vivo toxicology studies conducted through Contract Research Organizations (CROs).
- Contribute to impurity qualification, excipient safety evaluations, and overall risk assessment activities.
- Support the preparation of Safety Data Sheets (SDS) and related scientific documentation.
- Collaborate with cross-functional teams to ensure timely completion of research deliverables.
- Prepare regulatory and scientific documents, including:
- Impurity Qualification Reports
- Nonclinical Overview (Module 2.4)
- Nonclinical Summaries (Module 2.6)
- Permissible Daily Exposure (PDE) Documentation
- Nonclinical Sections of Risk Management Plans (RMPs)
- Identify toxicological data gaps using QSAR and in silico tools such as Derek Nexus and Sarah Nexus.
Educational Qualification
Candidates should possess one of the following qualifications:
- Master’s Degree in Pharmacy
- PhD in Pharmacy
- Master’s or PhD in Pharmacology
- Toxicology
- Medical Sciences
- Veterinary Sciences
- Biotechnology
- Biochemistry
- Other related Life Science disciplines
Preferred Skills
The ideal candidate should have knowledge of:
- Pre-Clinical Toxicology
- Toxicological Risk Assessment (TRA)
- Pharmacology
- Extractables and Leachables (E&L)
- Impurity Qualification
- Nonclinical Safety Assessment
- Regulatory Toxicology
- QSAR Modeling
- Predictive Toxicology
- Derek Nexus
- Sarah Nexus
- Safety Data Sheets (SDS)
- FDA, ICH, and ISO Guidelines
- CRO Study Management
- Statistical Data Interpretation
- Microsoft Word, Excel, and PowerPoint
- Scientific Writing
- Cross-functional Collaboration
- Communication and Presentation Skills
Experience Required
Baxter has not specified a fixed experience requirement.
Candidates with academic research experience, industrial toxicology experience, or practical exposure to pharmaceutical R&D, pre-clinical studies, or nonclinical safety assessments will be preferred.
Fresh postgraduates with strong research knowledge and relevant project experience may also have an advantage.
Salary Details
Baxter has not officially disclosed the salary for this position.
Based on current industry standards, professionals working as a Research Associate – Pre-Clinical Toxicology may expect an estimated annual salary ranging from ₹7 LPA to ₹12 LPA, depending on educational qualifications, research experience, technical expertise, and interview performance.
Additional employee benefits may include:
- Competitive salary package
- Health and insurance benefits
- Learning and development opportunities
- Global research exposure
- Career growth within Research & Development
- Employee benefits as per company policy
Job Location
Ahmedabad, Gujarat, India
How to Apply
Interested and eligible candidates can apply online through Baxter’s official careers portal before the application deadline.
Last Date to Apply: 11 August 2026
Applicants should ensure that their resume highlights their educational qualifications, research experience, toxicology knowledge, scientific publications (if any), and relevant technical skills before submitting the application.
Why Join Baxter?
Baxter is a globally recognized healthcare company committed to advancing patient care through scientific innovation and research. Working in Baxter’s Research & Development team provides professionals with the opportunity to contribute to global pharmaceutical development, regulatory toxicology, and nonclinical safety assessment while collaborating with international experts in a highly innovative environment.
Frequently Asked Questions (FAQs)
What is the job role offered by Baxter?
Baxter is hiring for the position of Research Associate – R&D Pre-Clinical Toxicology.
What qualifications are required?
Candidates should have a Master’s or PhD degree in Pharmacy, Pharmacology, Toxicology, Biotechnology, Biochemistry, Medical Sciences, Veterinary Sciences, or another related Life Science discipline.
Where is the job located?
The position is based in Ahmedabad, Gujarat.
What is the last date to apply?
The last date to submit the online application is 11 August 2026.
What are the key responsibilities?
The role involves pre-clinical toxicology research, toxicological risk assessment, nonclinical safety evaluation, regulatory documentation, CRO study management, impurity qualification, and scientific data analysis.
