Scientist - 2 Opening(s)
Job Description
Contribute to the development of a variety of pharmaceutical dosage forms from early to late phase development.
• Perform release and stability testing of drug products/active pharmaceutical ingredient according to approved methods
• Perform analytical method transfer activities
• Plan, perform, and document scientific experiments in support of drug substance/drug product development activities
• Develop, optimize and validate dosage form/active pharmaceutical ingredient analytical methods
• Provide analytical raw data documentation, evaluation and results interpretation for the development of drug products/active pharmaceutical ingredients
• Contribute to generation of lab procedures, reports, instructions or SOP’s, and to the evaluation of new lab equipment.
• Schedule and perform maintenance of lab instruments/equipment
• Work in accordance to cGMP and Novartis SOPs and policies.
• Perform release and stability testing of drug products/active pharmaceutical ingredient according to approved methods
• Perform analytical method transfer activities
• Plan, perform, and document scientific experiments in support of drug substance/drug product development activities
• Develop, optimize and validate dosage form/active pharmaceutical ingredient analytical methods
• Provide analytical raw data documentation, evaluation and results interpretation for the development of drug products/active pharmaceutical ingredients
• Contribute to generation of lab procedures, reports, instructions or SOP’s, and to the evaluation of new lab equipment.
• Schedule and perform maintenance of lab instruments/equipment
• Work in accordance to cGMP and Novartis SOPs and policies.
Desired Profile
Post graduate in Life Sciences / Chemistry / Biochemistry / Biochemical engineering.
Minimum 4 years in a GMP analytical laboratory, in the pharmaceutical industry.
Good English knowledge (oral and written)
Practical knowledge and hands-on experience with Dissolution and HPLC methods execution and stability assessment of dosage forms.
Working knowledge in the use of the following instrumentation: GC, titrimeters, UV/NIR/IR spectroscopy
Advanced computer skills: LIMS, chromatography data acquisition systems, MS office
Knowledge of cGMP requirements
Ability to interpret data and draw appropriate conclusions, to recommend additional experiments under moderate supervision
Good oral and scientific writing skills
Good multi-tasking with good time management skills. Ability to quickly adapt to changing work schedules
Effective team player, able to work in a flexible, dynamic working environment
Minimum 4 years in a GMP analytical laboratory, in the pharmaceutical industry.
Good English knowledge (oral and written)
Practical knowledge and hands-on experience with Dissolution and HPLC methods execution and stability assessment of dosage forms.
Working knowledge in the use of the following instrumentation: GC, titrimeters, UV/NIR/IR spectroscopy
Advanced computer skills: LIMS, chromatography data acquisition systems, MS office
Knowledge of cGMP requirements
Ability to interpret data and draw appropriate conclusions, to recommend additional experiments under moderate supervision
Good oral and scientific writing skills
Good multi-tasking with good time management skills. Ability to quickly adapt to changing work schedules
Effective team player, able to work in a flexible, dynamic working environment
Experience 2 - 7 Years
Education
UG - Any Graduate - Any Specialization
PG - M.Pharma - Pharmacy,M.Sc - Chemistry,M.Tech - Any Specialization, Chemical
Location Hyderabad / Secunderabad
Contact
Mr/Ms Novartis Healthcare Pvt Ltd
Telephone 67673047
Website http://www.novartis.com/
Reference 77915BR
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