Novartis has one of the most exciting product pipelines in the industry today. A pipeline of innovative medicines brought to life by diverse, talented and performance driven people. All of which makes them one of the most rewarding employers in their field.
Post : Scientist
Job Description
• Independently design, plan, organize, perform and document scientific experiments/GMP testing/plant activities under minimal supervision; multitask activities at a time; understand and meet customer needs - own and utilize complex tools/equipment or specialized facilities as an expert; schedule and perform maintenance and qualification of instruments/equipment - Proactively identify conflict situations and contribute with empathy to solutions
• Work according to appropriate standards as defined in Quality Manual, SOPs, ethical, health, safety, environment (HSE), and information security (ISEC) guidelines; lead initiatives to ensure proactive compliance and continuous improvement.
• Provide documentation of raw data, evaluate and interpret results, draw relevant conclusions independently and design next experiments; supervise project related scientific/technical activities. Review and verify raw data generated by others
• Write protocols, scientific reports, lab procedures or SOPs; write scientific documents intended for external partners (e.g., other line units, authorities, external companies) or for generation of registration documents under minimal supervision.
• Communicate, address and solve problems (e.g. deviations and unexpected results from experiments) within own and broader area of responsibility; communicate effectively across organizational interfaces; lead the transfer of know-how or procedures to other departments or external contractors, including troubleshooting and on-site training.
• For technical development units: Develop new methods/processes 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 role: Provide scientific and technical guidance; perform information and literature searches; actively foster knowledge exchange. Train and coach team members, temporary employees or employees under training; present scientific/technical results internally and contribute to publications, presentations and patents
• For project-focused role: Lead/coordinate assigned functional sub-teams; participate in function-specific teams and fulfill assigned project tasks and responsibilities under minimal supervision. Support non-project activities as needed, such as Op Ex, GDP coordinator etc.
Candidate Profile
• PhD with 2-3 years of experience on mass spectrometry Master of Science with 5-7 year of relevant experience Fluency in English language
• Awareness for safe handling of chemicals, potentially dangerous materials and equipment. Good theoretical and scientific knowledge in the relevant area (e.g. manufacturing, analytical, pharmaceutical)
• Proficient with laboratory and/or technical tools. Good knowledge of software and computer tools.
• Good documentation skills. Knowledge of current Good Manufacturing Practices (cGMP)
• Presentation skills
• Advanced scientific/technical writing skills Exclusive experience on independently carry out Impurity profiling using LCMS. GCMS and other allied techniques, interpretation of the results and scientific conclusions. Should have wide experience on qualification of genotoxic impurities, nitrosamine impurities using different mass spectrometric techniques
Additional Information
Experience : 2-7years
Qualification : M.Sc or PhD
Location : Hyderabad, AP
Industry Type : Pharma/ Healthcare/ Clinical research
Functional Area : Research & Development
End Date : 30th May, 2022
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