REQ-10079751
Jun 05, 2026
LOC_IN

About the Role

Key Accountabilities:

  • Independently plan, organize, perform and document scientific experiments /GMP testing /manufacturing plant activities under minimal supervision; handle several activities at a time -Take over responsibility for and utilize special tools /equipment or specialized facilities as an expert; schedule and perform maintenance and qualification of instruments / equipment -Proactively identify conflict situations and contribute to solutions -Work according to appropriate standards for quality, ethics, health, safety, environment protection, and information security; lead initiatives to ensure continuous improvement -Documentation of raw data, evaluate and interpret results; propose and actively support the design of next experiments.
  • Review and verify raw data generated by others; approval of tests / experiments performed by others -Write protocols, scientific reports or lab procedures based on templates or SOPs under minimal supervision -For technical development units: Develop new methods or optimize existing methods/processes (lab or plant); contribute to development and implementation of new technologies -For GMP units: ensure compliance to cGMP -For technology-focused roles: Perform information and literature searches under minimal guidance. Actively foster knowledge exchange.
  • Train and coach associate scientists, technicians, temporary employees and employees under training / education -For project-focused role: Participate in function-specific sub teams and fulfill assigned project tasks and responsibilities under supervision -Uses professional concepts and company's policies and procedures to solve a wide range of difficult problems in imaginative and practical ways.
  • Establish innovative solutions for verification and control of critical quality attributes, critical material attributes or critical process parameter in cooperation with other colleagues.
  • Establish control procedures and specifications and review test procedures.
  • Generate scientific documents to hand over to internal and / or external partners (e.g., MST, TechOps, authorities, external companies) and support generation of international registration documents under minimal supervision.
  • If assigned this task, maintenance of infrastructure / equipment and required investments ( e.g. system ownership) -Generate lab procedures or SOP’s, generate protocols and reports -Lead technical meetings during product development at the local level as well as on the level of global network -Report and present scientific /technical results internally and contribute to publications, presentations and patents.

Essential Requirements:

  • Deep expertise in Chromatography & Separation Science, including method selection, optimization, and troubleshooting across analytical workflows.
  • Strong experience in dissolution testing, with sound understanding of method development, validation, and interpretation for drug products.
  • Proven capability in analytical method development for drug products, particularly solid oral dosage forms, ensuring robustness, accuracy, and regulatory compliance.
  • M.Pharm./M.Sc. with up to 10 years of relevant experience, or Ph.D. with demonstrated experience in a related domain.

    Role Requirements

    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.
    Read our handbook (PDF 30 MB)

    DIV_GD
    Development
    LOC_IN
    Hyderabad (Office)
    LOC_IN
    FCT_RD
    Full time
    Regular
    No
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    REQ-10079751

    Expert -Science & Technology

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