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PHARMA JOBS POST > Hiring > Teva Pharmaceuticals is Hiring: Start Your Career as a Quality Control Analyst Now!
HiringQuality Control

Teva Pharmaceuticals is Hiring: Start Your Career as a Quality Control Analyst Now!

ADMIN
Last updated: September 3, 2024 3:52 pm
ADMIN 2 years ago
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Teva Pharmaceuticals Hiring for Quality Control Analyst Position

Contents
Quality Control AnalystWho we areHow you’ll spend your dayYour experience and qualificationsReports To

Quality Control Analyst

Location:  

Gajraula, India, 244235

Company:  Teva Pharmaceuticals

Job Id:  57810

Who we are

Together, we’re on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It’s a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world’s leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization’s Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we’re always looking for new ways to continue making a difference, and new people to make a difference with.

How you’ll spend your day

  • Candidate should be SME in Wet analysis Laboratory.
  • Investigations of Deviations, OOS, OOT, Alert Limit, Action Limit and Atypical Analytical Test results
  • Ensuring adequacy and timely completion of all wet laboratory Investigation, change controls and CAPA.
  • Responsible to explain above area in case of customer, regulatory, any other external or internal audits.
  • Overseeing the operations of the laboratory on a day-to-day basis, per shift, to ensure GXP in laboratory.
  • Review daily calibration data. 
  • Reviewed analytical data on daily basis.
  • Worked performed in GXP environment.
  • Raising the purchase requisition for arranging the items related to wet laboratory.
  • Preparing the document and STP related to wet analysis laboratory.
  • To execute the protocol and report to perform the validation/study activities.
  • Instrument Calibration, Preventive maintenance and Malfunctioning Management.

Your experience and qualifications

  • Msc chemistry
  • 10 to 12 years

Reports To

Group Leader Quality Control

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By ADMIN
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Sanyasi Pradhan, M.Pharm, is a pharma professional and entrepreneur with a strong background in the pharmaceutical industry, writing on jobs and global pharma updates
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