Together, we\xe2\x80\x99re on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It\xe2\x80\x99s 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\xe2\x80\x99s leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization\xe2\x80\x99s 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\xe2\x80\x99re always looking for new ways to continue making a difference, and new people to make a difference with.
How you\xe2\x80\x99ll spend your day
FDA Approved in Microbiology.(should be Preferred)
Investigations of Deviations, OOS, OOT, Alert Limit, Action Limit and Atypical Analytical Test results, Instruments errors, Change Control and temporary changes.
Responsible for preparation of quality management system documents.
Raising the purchase requisition for arranging the items related to microbiology
Preparing the document and STP related to microbiological analysis
To execute the protocol and report to perform the validation/study activities.
Instrument Calibration, Preventive maintenance and Malfunctioning Management related to microbiology.
Ensure Adequacy and timely completion of Investigation, Change controls, and CAPA\xe2\x80\x99s of all above areas.
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.
Should be skilled to handled regulatory inspection.
To ensure corrective and preventive actions are implemented and are effective.
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