Sachin Badgujar Email & Phone Number | Review Compliance level of site for deficiency. - Coordinate With auditors and site teams for regulatory and customer inspection/ audit at site to meet regulatory expectations. - Prepare draft of compliance to audit observation and check whether it is in line with cGMP requirement to avoid regulatory action and continual improvements. - Drive continuous improvement initiatives in CQA to facilitate adherence to cGMP. - Review annual product quality review report at units for completeness and data correctness to ensure compliance to cGMP requirements and audit readiness. - Investigations of various non- conformances of QMS & determine Root cause and CAPA, as per cGMP requirements

Sachin Badgujar

Review Compliance level of site for deficiency. - Coordinate With auditors and site teams for regula...
Indore, Indore, India

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Sachin Badgujar’s Email sachin.badgujar@cipla.com

Sachin Badgujar’s Phone Numbers

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Sachin Badgujar’s Location Indore, Indore, India

Sachin Badgujar’s Current Industry Cipla

Sachin Badgujar’s Prior Industry Lupin Pharmaceutical | Macleod Pharmaceutical | Rcpiper Shirpur

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Sr. Executive

2020-10-01 00:00:00 - Present

Executive at Lupin pharmaceutical Ltd.

2019-01-01 00:00:00 - 2020-10-01 00:00:00

Quality Control Officer

2016-05-01 00:00:00 - 2019-01-01 00:00:00

Post Graduate Student

2014-08-01 00:00:00 - 2016-06-01 00:00:00

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Sachin Badgujar is a Review Compliance level of site for deficiency. - Coordinate With auditors and site teams for regulatory and customer inspection/ audit at site to meet regulatory expectations. - Prepare draft of compliance to audit observation and check whether it is in line with cGMP requirement to avoid regulatory action and continual improvements. - Drive continuous improvement initiatives in CQA to facilitate adherence to cGMP. - Review annual product quality review report at units for completeness and data correctness to ensure compliance to cGMP requirements and audit readiness. - Investigations of various non- conformances of QMS & determine Root cause and CAPA, as per cGMP requirements