Novartis have more than 130 years of experience treating patients. Sandoz, a division of Novartis, is a global leader in generics and biosimilars and is committed to playing a leading role in improving access to medicines worldwide.
Post : Scientist - Formulation Development
Job Description
Position Purpose
Independently plan and perform scientific experiments or GMP testing or develop processes in the plant processes for the preparation and timely delivery of drug products (DP), processes and procedures; maintain and qualify equipment/infrastructure and manage operational aspects in lab or plant as assigned.
KEY RESPONSIBILITIES:
Your responsibilities include, but are not limited to:
• Independently plan, organize, perform and document scientific experiments/ GMP testing/ 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 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; propose and provide input for the design of next experiments. Review and verify raw data generated by others; approval of test/experiments performed by others
• Write protocols, scientific reports or lab procedures based on templates or SOPs under minimal supervision . Recognize, communicate, address and solve problems (e.g. deviations and unexpected results from experiments) within own and broader area of responsibility; actively transfer know-how or procedures to other departments or external contractors, including troubleshooting and on-site training
• For technical development units: Develop new methods or optimize existing methods (lab or plant); contribute to development and implementation of new technologies.
For GMP units: ensure compliance to cGMP
• For technology-focused role: 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
• Support non-project activities as needed, such as Op Ex, GDP coordinator etc.
Candidate Profile
Minimum Requirements
• Master of Science with atleast 4 year of relevant experience. Fluent in English (oral and written) Basic skills in local site-language, as required for the position
• 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). Advanced scientific/technical writing skills.
Additional Information
Experience: min. 4 years
Qualification: Master of Science
Location: Hyderabad
Industry Type: Pharma/ Healthcare/ Clinical research
Functional Area : Research & Development
End Date : 30th July, 2022
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