Santosh Kumar
Quality Assurance- Manager and MR at Benzo Chem Industries Pvt. Ltd. - India- Claim this Profile
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Bio
Experience
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Benzo Chem Industries Pvt. Ltd. - India
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Chemical Manufacturing
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1 - 100 Employee
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Quality Assurance- Manager and MR
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Nov 2012 - Present
Responsible for introduction & implementation of SOPs covering the system to be implemented in different departments i.e. QA, QC, PD, Maintenance, warehouse e.t.c to meet the regulatory requirements as well as as quality systems. Responsible for vedor qualification and Audit. Handling and achievements of lots of regulatory Audit as well as customer audit based on GMP and ISO. Responsible for introduction & implementation of SOPs covering the system to be implemented in different departments i.e. QA, QC, PD, Maintenance, warehouse e.t.c to meet the regulatory requirements as well as as quality systems. Responsible for vedor qualification and Audit. Handling and achievements of lots of regulatory Audit as well as customer audit based on GMP and ISO.
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Vardhman Chemtech Ltd - India
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India
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Pharmaceutical Manufacturing
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1 - 100 Employee
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Executive - QA
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Sep 2010 - Oct 2012
Responsible for introduction & implementation of SOPs covering the system to be implemented in different departments i.e. QA, QC, PD, Maintenance, warehouse e.t.c to meet the regulatory requirements as well as as quality systems. Responsible for vedor qualification and Audit. Handling and achievements of lots of regulatory Audit as well as customer audit based on GMP and ISO. Responsible for introduction & implementation of SOPs covering the system to be implemented in different departments i.e. QA, QC, PD, Maintenance, warehouse e.t.c to meet the regulatory requirements as well as as quality systems. Responsible for vedor qualification and Audit. Handling and achievements of lots of regulatory Audit as well as customer audit based on GMP and ISO.
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QA-Executive
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Aug 2007 - Sep 2010
Handling the QA deparment independently and facing the lots of vendor audit as well as the customer Audit. Expert in Process validation and equipment qualification. Handling the QA deparment independently and facing the lots of vendor audit as well as the customer Audit. Expert in Process validation and equipment qualification.
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QA - Officer
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Sep 2005 - Jul 2007
Responsible for review of all deparmental SOPs and Batch Manufacturing record and implemented into the system. Review the executed data of Production batches. Participants to perform the internal Audit. Handling of change control, deviation, market complaints, OOS and prepration of APR. Responsible for review of all deparmental SOPs and Batch Manufacturing record and implemented into the system. Review the executed data of Production batches. Participants to perform the internal Audit. Handling of change control, deviation, market complaints, OOS and prepration of APR.
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ALLYCHEM LABORATORIES P.LTD.
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Chemical Manufacturing
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1 - 100 Employee
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Sr. Chemist - Quality Assurance
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Apr 2003 - Aug 2005
Responsible for review of all deparmental SOPs and Batch Manufacturing record and implemented into the system. Review the executed data of Production batches. Participants to perform the internal Audit. Handling of change control, deviation, market complaints, OOS and prepration of APR. Responsible for review of all deparmental SOPs and Batch Manufacturing record and implemented into the system. Review the executed data of Production batches. Participants to perform the internal Audit. Handling of change control, deviation, market complaints, OOS and prepration of APR.
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