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Teva Physical R&D Researcher II - TAPI 
India, Uttar Pradesh, Greater Noida 
683735480

07.04.2025
How you’ll spend your day
  • Perform Polymorph screening as per guideline.
  • Follow cGMP Documentation and EHS compliance at workplace
  • Perform Virtual and Experimental Screen and evaluate all literature that relates to solid-state issues.
  • Screen new forms by performing stress tests and File ASAP new forms in patent application
  • Analyze laboratory samples by XRD, DSC, TGA and other characterization techniques.
  • Assess kinetic stability and interconversions and produce scheme of all polymorphic transitions
  • Produce solubility curves of different polymorphs and assess thermodynamic stability relationships
  • Develop detection methods to assess polymorphic purity and monitor in the laboratory samples
  • Support the development of the crystallization process with full characterization
  • Monitoring stability and physical properties of micronized/milled materials
  • Perform calibration, method development, method validation, and troubleshooting using various instruments like PXRD, DSC, TGA and Particle size analyzer
  • Knowledge of various regulatory guidelines w.r.t. method development, product development, and documentation.
Your experience and qualifications

Qualification: MSc Chemistry / B Tech (Chemical Engineer)

Experience:

  • 1-5 years of experience in relevant industry and profile
  • Experience with quantum chemistry, molecular modeling,
  • Programming in Python, R, or MATLAB.
  • Experience with machine learning (ML) algorithms for chemical data (e.g., regression, clustering, neural networks).
  • Familiarity with chemoinformatics libraries (e.g., RDKit, Open Babel).
  • Knowledge of data visualization (Matplotlib, Seaborn, Plotly).
  • Molecular docking and simulations (e.g., AutoDock, GROMACS, Gaussian).
  • Use of AI/ML models for material science or drug discovery.
  • Polymorph Screening experience
  • Analyze laboratory samples by XRD, DSC, TGA and other characterization techniques
  • Follow cGMP Documentation and EHS compliance at workplace
  • Support the development of the crystallization process with full characterization

Internships or work experience in pharmaceutical, chemical, or biotech industries