Teva Quality Control Technician 

India, Uttar Pradesh 

30546788

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.

Minimum 3 to 4 years of experience.

M.Sc. / Pharm graduates