Analytical Scientist Post in Novartis Freshers may apply
A global healthcare leader, 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.
• Individually performs and manages innovation, method development, method validation under guidance.
• Independently performs prestability/ stability testing and all other analytical related activities for Global OTC products.
• Acquisition of all technical competencies required for analytical development at work.
• Participate in project teams and assist in troubleshoot and finding solutions.
• Conducts experiments, investigations, and special testing as needed for problem solving, to address regulatory issues, or to characterize drug substances/ drug products.
• MSc / M Pharm with 0 - 2 years of relevant experience.
Experience: 0-2 Years
Location: Hyderabad
Education: M.Sc, M.Pharm
Industry Type: Pharma/ Biotech/Clinical Research
Functional Area: R&D
Division: Pharma
Job Type: Full Time
Employment Type: Permanent
Job ID: 126818BR
End Date: 24th Sep., 2013 (APPLY NOW, POSITION MAY CLOSE TODAY ITSELF)
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A global healthcare leader, 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: Analytical Scientist - I
Job Description
• Individually performs and manages innovation, method development, method validation under guidance.
• Independently performs prestability/ stability testing and all other analytical related activities for Global OTC products.
• Acquisition of all technical competencies required for analytical development at work.
• Participate in project teams and assist in troubleshoot and finding solutions.
• Conducts experiments, investigations, and special testing as needed for problem solving, to address regulatory issues, or to characterize drug substances/ drug products.
• Work closely with members of cross functional teams at different locations.
• Accountable for managing projects against timelines while maintaining high quality standards.
• Maintains GMP compliant, state-of-the-art analytical laboratories.
• Perform all laboratory work with proper planning and scheduling of jobs.
• Accountable for consistently meeting the targets and KPI’s for self.
Key Distinguishing Responsibilities
• Follow GMPs, SOPs, HSE requirements and other applicable regulations.
• Performs analytical method development, method validation and Method Transfers under
supervision.
• Write / Review SOPs, qualification documents and protocols & reports of method development,
method validation and method transfer.
• Review laboratory notebooks (routine testing).
• Execution of Prestability / GMP Stability samples and maintenance of laboratory database.
• Suggest potential equipment needed for analytical development.
• Trouble shoot scientific and instrument related challenges with limited supervision.
• Train associates on analytical methods and instrumentation case by case basis. Keep abreast on the latest changes in analytical science with limited supervision.
• Desired knowledge of chemical principles, analytical techniques, analytical instrumentation, GxPs, validation and allied areas.
• Current knowledge of chemical and Analytical sciences is desirable.
• Good communication skills.
• Experience in managing analytical or stability projects is desirable.
• Ability to solve complex scientific problems.
• Computational skills.
• Sound working knowledge of Computers.
• Accountable for managing projects against timelines while maintaining high quality standards.
• Maintains GMP compliant, state-of-the-art analytical laboratories.
• Perform all laboratory work with proper planning and scheduling of jobs.
• Accountable for consistently meeting the targets and KPI’s for self.
Key Distinguishing Responsibilities
• Follow GMPs, SOPs, HSE requirements and other applicable regulations.
• Performs analytical method development, method validation and Method Transfers under
supervision.
• Write / Review SOPs, qualification documents and protocols & reports of method development,
method validation and method transfer.
• Review laboratory notebooks (routine testing).
• Execution of Prestability / GMP Stability samples and maintenance of laboratory database.
• Suggest potential equipment needed for analytical development.
• Trouble shoot scientific and instrument related challenges with limited supervision.
• Train associates on analytical methods and instrumentation case by case basis. Keep abreast on the latest changes in analytical science with limited supervision.
• Desired knowledge of chemical principles, analytical techniques, analytical instrumentation, GxPs, validation and allied areas.
• Current knowledge of chemical and Analytical sciences is desirable.
• Good communication skills.
• Experience in managing analytical or stability projects is desirable.
• Ability to solve complex scientific problems.
• Computational skills.
• Sound working knowledge of Computers.
Experience
• MSc / M Pharm with 0 - 2 years of relevant experience.
Additional Information:
Experience: 0-2 Years
Location: Hyderabad
Education: M.Sc, M.Pharm
Industry Type: Pharma/ Biotech/Clinical Research
Functional Area: R&D
Division: Pharma
Job Type: Full Time
Employment Type: Permanent
Job ID: 126818BR
End Date: 24th Sep., 2013 (APPLY NOW, POSITION MAY CLOSE TODAY ITSELF)
For more Jobs visit Jobes Mantra
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