REQ-10087686
Sep 17, 2026
India

Summary

-Directs and manages toxicological and/or pathological studies data in preclinical safety and efficacy testing on new and marketed products. Establishes policies for use of contract laboratories and consultants. Support audit and HAQ from FDA and other regulatory agencies. Support in conducts and summarizes toxicology safety studies on new drug substances. Improves methods for drug safety evaluation; analyzes and prepares reports of findings; performs advisory functions in dealing with items found to contain toxic material; and completes and/or reviews toxicology section of submissions to regulatory agencies.
-Senior Scientist I:Independently conceives and executes experiments that implement project strategy and test independently‐ generated hypotheses. May bring new technique(s) into lab/ process. Increasingly proficient at supporting multiple activities in parallel. Provides input to operational and/or strategic discussions related to own technical knowledge.

About the Role

Major accountabilities:

  • Senior Scientist I:Designs/executes experiments and identifies next steps based on analysis of own data and data from other lab contributors.
  • Independently modifies existing lab techniques/processes and implements techniques new to the lab.
  • Communicates results and conclusions to project meetings.
  • May provide input to internal/ external publications including writing relevant sections.
  • Skilled in collaboration across project team labs.
  • May suggest/build new network connections within existing project teams.
  • Routinely trains members of lab and broader project team in familiar techniques.
  • Expected (if needed) to undertake organizational responsibility (such as equipment power user, lab safety rep).
  • Accountable for increasingly complex experiments; key contributor to the success of drug discovery, technology, and/or early development projects.
  • Brings ideas from a concept or question to a decision in experimental design, based on previous observations.
  • Reporting of technical complaints / adverse events / special case scenarios related to Novartis products within 24 hours of receipt

Minimum Requirements:

  • Graduate/ Postgraduate in Life Sciences with 5-7 years relevant experience working in pharmaceutical GLP setting.
  • Good working knowledge of regulatory compliance requirements
  • Knowledge of animal welfare requirements related to study conduct
  • Good communication skills, and excellent logistical/planning skills
  • Previous experience with software for online information and program management is a plus

Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture

Benefits and Rewards: Learn about all the ways we’ll help you thrive personally and professionally.
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Biomedical Research
Development
India
Hyderabad (Office)
Research & Development
Full time
Regular
No

Accessibility and accommodation

Novartis is committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to perform the essential functions of a position, please send an e-mail to [email protected] and let us know the nature of your request and your contact information. Please include the job requisition number in your message.

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REQ-10087686

Senior Scientist 1, Toxicology

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