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Senior Scientist

8.00 to 13.00 Years   Hyderabad   19 Nov, 2019
Novartis Healthcare Pvt Ltd
Job LocationHyderabad
EducationNot Mentioned
SalaryNot Disclosed
IndustryMedical / Healthcare
Functional AreaR&D / Product DesignGeneral / Other Software
EmploymentTypeFull-time

Job Description

Your responsibilities: Your responsibilities include but are not limited to:

  • Provide expert technical support to our development projects, drive appropriate biopharmaceutics assessment to the development phase of the project and provide input to the drug product design in development projects, working in partnership with TRD subteam and key stakeholders (e.g. PK Science and Translational Medicine).
  • Plan, perform evaluate and report in close collaboration with experts from other areas in silico (e.g. PBBM via Gastroplus ) and in vitro tests (eg biorelevant dissolution, permeability testing), or in vivo studies (e.g. RelBA and BE to bridge formulation changes).
  • Contribute to the understanding of the inter-relationships of the drug s properties, the dosage form and drug absorption in line with target product profile.
  • Proactively identifying potential scientific, technological gaps, proposing creative solutions and ensuring appropriate communication within and across units.
  • Author biopharmaceutic relevant reports (e.g. absorption modeling, or biorelevant dissolution), including relevant CMC documentation for clinical and marketing applications.
  • Strong contribution to advance science, technology and innovation within the area of biopharmaceutics aiming to obtain better predictive biopharmaceutics methods or improved drug delivery, includes identifying and contributing to external consortium or initiative

Minimum requirements

What you ll bring to the role:

  • Minimum: M. Pharm, M. Tech or equivalent Desirable: Advanced degree in a scientific or relevant discipline such as pharmaceutical sciences, chemical engineering or life sciences (MS or Ph.D.)
  • Good knowledge of English (oral and written).
  • Minimum 8 years experience in the pharmaceutical industry, preferably in biopharmaceutic, pharmaceutical science and/or pharmacokinetic.
  • An understanding of drug development process and the contribution of pharmaceutical development from lead optimization to launch Proven leadership experience in managing projects ideally in a global matrix environment
  • Excellent knowledge of biopharmaceutics tools for the characterization of API and dosage form and modelling and simulation software in the biopharmaceutic area.
  • Ability to interpret and analyze a variety of different data to provide scientific direction to others.
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Keyskills :
researchvalidation documentationapi hplcinternational joint ventures in vivoin vitro

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