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Teva Analytical R&D Analyst 
India, Uttar Pradesh 
298111618

24.11.2024
How you’ll spend your day
  • To participate in method development and routine analytical support to pilot and CRD for raw materials, intermediates, in-process samples and drug substance.
  • Good knowledge of wet chemistry.
  • Familiar with HPLC, UPLC, GC, GCHS, FTIR, PSD, TGA and other analytical techniques.
  • Stability studies and Forced Degradation studies for drug substance as per ICH guidelines.
  • Calibration and Maintenance of sophisticated Instruments, such as Balance, HPLC, GC, IR, Karl Fischer, Melting point analyzer and Polarimetry.
  • Conducting routine analysis of CRD and pilot samples as per set procedures.
  • Documentation as per GMP requirements.
  • Adhering to safety norms and safe culture in lab.
  • To ensure online data compilation and recording to have full compliance.
  • To contribute in maintaining analytical laboratory as per the GLP and safety requirements.
  • To contribute in providing necessary support to QC during validation batches as well as in routine (Need based in justifiable fashion).
  • To support in full-filling the regulatory/customer related tasks related to commercial/pipeline products (as per real need and assigned task).
  • To participate in departmental trainings/discussion programs.
  • Any other assignments allocated by manager/team leader as per time need.
Your experience and qualifications
  • MSc. in Organic Chemistry/Analytical chemistry
  • Work Experience: Required: 3-5 years
Reports To

Manager Analytical R&D

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