Job Details
Company: Sun Pharmaceutical Industries Ltd
Business Unit: R&D1 Regulatory Affairs
Job Grade: G11A/G10
Responsibilities
- Design, execute, and interpret preclinical in vivo studies using rodent/non-rodent models.
- Conduct, develop and supervise cell-based and biochemical assays.
- Perform statistical analysis (ANOVA, post-hoc tests) using appropriate software, interpret experimental outcomes, and prepare high-quality scientific documents including study reports, manuscripts, and regulatory-ready summaries.
- Contribute to translational research and cross-functional collaboration with project teams.
Qualifications
Educational Qualification: PhD in Pharmacology.
Experience: 3-8 years.