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 drove people. All of which makes them one of the most rewarding employers in their field.
Post: Associate Scientist 2
M.Pharm. or equivalent Desirable - Advanced degree in a scientific or relevant discipline (PhD or equivalent). English
1. Directly related experience as Associate scientist M.Pharm. with 1 to 5 years of experience or PhD in Science with focus on pharmaceutical sciences and technology (e.g. Pharmacy, Chemistry)
2. Awareness of safe handling of chemicals, potentially dangerous materials and equipment.
3. Adequate scientific or technical knowledge in a specific area (e.g. synthetic, analytical, galenical).
4. Basic knowledge in scientific/technical areas of collaboration.
5. Good knowledge of laboratory and/or technical tools.
6. Adequate knowledge of software and computer tools.
7. Creative thinking and effective interdisciplinary collaboration with other functions.
8. Basic presentation skills and scientific/technical writ-ing skills. 9. Good communication skills and basic organizational, planning and negotiation skills.Job Description
1. Support development of early and late phase NCE development for solid, liquid, parenteral and topical dosage forms (including poorly soluble compounds).
2. Support entire drug product development process starting with first pre-formulation studies up to the manufacturing process transfer to production and the provision of the required documentation to allow worldwide registration
3. Support development of robust formulations and processes through optimization, scale-up and validation work applying QbD principles incl. risk assessments and DoEs
4. Provide documentation of raw data, evaluation and contribute to interpretation of results. Provide input for the selection of next experiments.
5. Communicate and address problems, perform safety and literature searches under guidance from more experienced team members.
2. Support entire drug product development process starting with first pre-formulation studies up to the manufacturing process transfer to production and the provision of the required documentation to allow worldwide registration
3. Support development of robust formulations and processes through optimization, scale-up and validation work applying QbD principles incl. risk assessments and DoEs
4. Provide documentation of raw data, evaluation and contribute to interpretation of results. Provide input for the selection of next experiments.
5. Communicate and address problems, perform safety and literature searches under guidance from more experienced team members.
Key Performance Indicator
1. Adherence to quality, quantity and timelines for all assigned tasks.
2. Adherence to Novartis standards, in particular, quality, ethical, health, safety, and environmental standards (HSE), and information security standards (ISEC.
3. Ensures reproducibility of experiments and results.
4. Refer to annual individual and team objective setting
1. Adherence to quality, quantity and timelines for all assigned tasks.
2. Adherence to Novartis standards, in particular, quality, ethical, health, safety, and environmental standards (HSE), and information security standards (ISEC.
3. Ensures reproducibility of experiments and results.
4. Refer to annual individual and team objective setting
Additional Information :
Experience: 1 to 5 years
Qualification : M.Pharm./M.Sc. or PhD
Location: Hyderabad
Industry Type: Pharma
Functional Area : Research & Development
End Date: 30th, May 2018
Experience: 1 to 5 years
Qualification : M.Pharm./M.Sc. or PhD
Location: Hyderabad
Industry Type: Pharma
Functional Area : Research & Development
End Date: 30th, May 2018
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