Pharma Job Vacancies For MPharma at Novartis
Novartis, one of the world’s leading pharmaceutical companies, is hiring for an Expert – Science and Technology in its global Analytical R&D (ARD) division in Telangana, India. This role offers a dynamic opportunity for professionals with a strong background in analytical method development to contribute to innovative drug substance and product pipelines. If you’re passionate about science, compliance, and transforming patient outcomes, this full-time position at Novartis could be your next big move.
Job ID: 10057517
Summary
Design, plan, perform, interpret and report results of scientific experiments for the method development of drug substances (DS) and drug products (DP) within global ARD. Lead and manage all project/local network activities, support/coach team members, participate in sub-teams and contribute to overall TRD strategies and goals.
About the Role
Major activities
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- Develop and qualify various analytical methods (e.g., fast LC, titration, dissolution).
- Provide analytical and technical support to PHAD/project team at various stages of product development (e.g., CSF, FMI and LCM).
- Design and author analytical documents (e.g., Analytical methods, Stability protocols/reports, Excipient compatibility (EC) protocol/reports; APS protocols/reports, etc.)
Ideal background
Education and experience: M.Sc. /M. Pharm/ Ph.D. with relevant experience.
Languages: Good knowledge of English and
site language (oral and written).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? Join Novartis Network
Why This Job
- Be a part of global R&D for cutting-edge therapies.
- Develop, qualify, and support analytical methods across drug development stages.
- Collaborate across interdisciplinary teams, from formulation to regulatory.
- Lead the design of critical documentation like stability protocols, EC/APS reports, and more.
- Contribute to Novartis’ mission of reimagining medicine for millions of patients worldwide.
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