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Teva Quality Control Technician 
India, Uttar Pradesh 
580225539

25.06.2024
How you’ll spend your day
  1. Person having Knowledge about the HPLC/GC chromatography and wet lab activity.
  2. Person having the knowledge of analytical tech transfer & method validation of HPLC/ GC.
  3. Analysis of stability samples & working standard qualification activity as per defined procedure & monograph.
  4. Maintaining a set of procedure supporting to ATS department for (GMP & GLP) techniques implementation.
  5. Maintaining a system of methods and specification for all materials and products.
  6. Data filling and maintaining the log books, certificate, stability report and stability data in archive.
  7. Monitoring of stability studies with respect to ICH Q-1 and conducting analytical method validation activity according to ICH Q-2.
  8. To initiate the LIR / OOS if any procedural gap related with SOP / monograph during routine activity.
  9. Qualifications of all analytical instruments should be maintained in stability Section.
Your experience and qualifications

Minimum 3 to 4 years of experience.

M.Sc. / Pharm graduates