Teva Quality Control Technician 

India, Madhya Pradesh, Gwalior 

722543193

• Maintaining a set of procedure supporting to ATS department for (GMP & GLP) techniques implementation.
• Maintaining a system of methods and specification for all materials and products.
• Analysis of stability samples & working standard qualification activity as per defined procedure & monograph.
• Data filling and maintaining the logbooks, certificate, stability report and stability data in archive.
• Monitoring of stability studies with respect to ICH Q-1 and conducting analytical method validation activity according to ICH Q-2.
• To initiate the LIR / OOS if any procedural gap related with SOP / monograph during routine activity.
• Qualifications of all analytical instruments should be maintained in stability Section.
• Follow the defined safety procedure during day to day activity in laboratory.
• Any other job assigned by Manager Quality Control.

• Experience range should be minimum 3 - 4 Years
• Should be Bsc/MSc
• Good understanding of Quality Control, Understanding of GMP & GLP

Group Leader Quality Control