Are you a passionate scientist with expertise in preclinical research and toxicology? Dr. Reddy’s Laboratories Ltd., a global leader in pharmaceuticals, is hiring a Scientist – Preclinical to join their Integrated Product Development Organization (IPDO) in Hyderabad, India. This role offers a unique opportunity to contribute to groundbreaking drug development, focusing on generics, complex generics, and differentiated products. With a mission to accelerate access to affordable medicines, Dr. Reddy’s is seeking a professional with 5-6 years of experience to drive preclinical strategies and toxicological assessments.
About Dr. Reddy’s Laboratories
Founded in 1984, Dr. Reddy’s is a multinational pharmaceutical company with a presence in 66 countries. With over 24,000 employees, the company is committed to innovation, affordability, and sustainability, aiming to reach 1.5 billion patients by 2030. The IPDO integrates deep science and cutting-edge technology to develop therapies that transform lives globally.
Roles and Responsibilities
As a Scientist – Preclinical, you will play a pivotal role in advancing drug development through:
- Toxicological Risk Assessments: Prepare Permissible Daily Exposure (PDE) and Occupational Exposure Limit (OEL) monographs for excipients, impurities, extractables, and leachables.
- Query Resolution: Address toxicological hazard queries from cross-functional teams, including Safety and Plant teams, for actives, intermediates, and Key Starting Materials (KSMs).
- Preclinical Strategy: Support the development of preclinical strategies for complex generics and design in-vitro/in-vivo studies.
- CRO Support: Assist in qualifying Contract Research Organizations (CROs), conducting GLP/Non-GLP study audits, and monitoring studies.
- Literature Analysis: Conduct extensive literature searches and analyze peer-reviewed scientific reports and regulatory guidelines.
- Collaboration: Work with internal teams and external stakeholders to align toxicological assessments with project goals and regulatory requirements.
- SOP Adherence: Prepare, maintain, and follow Standard Operating Procedures (SOPs).
Qualifications
To excel in this role, candidates should have:
- Educational Background: Master’s Degree (M.V.Sc or M. Pharm in Pharmacology).
- Experience: 3-6 years in the pharmaceutical industry, specializing in preclinical research or toxicology risk assessments.
- Technical Skills:
- Expertise in toxicological risk assessment methodologies, PDE, and OEL monographs.
- Proficiency in analyzing physicochemical, clinical, and non-clinical data.
- Knowledge of EMEA, FDA, ICH, ISO, and ASTM guidelines.
- Familiarity with QSAR tools, BMDS, and MPPD software.
- Experience in preclinical drug development and regulatory requirements for ANDA/NDA filings.
- Understanding of GLP/OECD guidelines and toxicity study protocols.
- Ability to perform statistical analysis and QC checks on study data.
- Behavioral Skills:
- Strong communication and interpersonal skills.
- Excellent analytical and problem-solving abilities.
- Ability to collaborate across teams and manage multiple priorities under tight deadlines.
Benefits
Dr. Reddy’s offers a supportive and inclusive work environment with:
- Career Growth: Personalized learning programs and professional development opportunities.
- Comprehensive Benefits: Relocation support, family benefits, medical, and life coverage.
- Work Culture: A dynamic, empathetic, and inclusive culture driven by the motto, “Good Health Can’t Wait.”
- Global Impact: Contribute to innovative therapies reaching over 55 markets worldwide.
How to Apply
Ready to make a difference in global healthcare? Apply now through the Dr. Reddy’s career portal. Submit your resume and cover letter highlighting your preclinical and toxicology expertise. Applications are reviewed on a rolling basis, so apply by September 26, 2025, to be considered.
FAQs
Q: What is the work environment like at Dr. Reddy’s?
A: Dr. Reddy’s fosters an inclusive, discrimination-free workplace that values diversity and collaboration, supporting employees with a purpose-driven culture.
Q: Is prior experience with CROs required for this role?
A: While not mandatory, experience with CRO qualification and study monitoring is highly desirable and will strengthen your application.
