Experience

Arch Pharmalabs, Ltd.

• India
• Pharmaceutical Manufacturing
• 400 - 500 Employee

• Assitant Manager quality control

  • May 2008 - Present

  Role:  Check and document calibration and analysis record.  Check and maintain the records of stability study and control samples.  Coordinate with Q.C. Chemist/officer and production supervisors regarding daily analysis  Ensure entries & signature missing in the record.  Preparation of RM, Intermediate, Finished goods and packaging material specification and worksheets.  Preparation of calibration, stability study yearly planners.  Verify the records of lab reagents, volumetric solutions and buffer solution.  Execute of IO/OQ/PQ for laboratory instruments  Check accurate documented data and test results in appropriate logbooks, hard books or result sheets.  Review and check analytical data generated by other analyst  Arrange sample, prepared label and documents for submission to external test laboratories.  Write and update standard operating procedures as per requirement. Execute analytical validation for finished product as per approved protocols Issue the analytical work sheet to analyst for perform the test Do routine maintenance & calibration of respective instrument from external agency. Strong oral/written communication skills. Strong attention to details Good and thorough operating exposure to SAP. NOTABLE CONTRIBUTIONS: Quality Control Ensuring stringent adherence to quality testing as per SOP, identifying gaps, trouble shootings and taking corrective action Handling activities regarding scheduling /indenting as per production planning, checking reports of all products, intermediates and finished products etc. Preparation of ISO documents Show less



S I GROUP INDIA LTD

• QC Officer

  • Sep 1998 - May 2008

  Role: To act as Service Department to Warehouse, Production,Utility & Q.A. arrange to analyse to raw materials, packing material, intermediates, solvents, water, finished Goods as per laid down procedures and specifications. To maintain records of all analysis as per format. To ensure validation of equipments like HPLC, GC is done & Records are maintained. To calibrate all laboratory equipments as per schedule and update records. To co-ordinate with production department, warehouse and Q.A. regarding dispatch of finished goods. To store control samples of all finished goods dispatched in designated containers at controlled atmosphere. Show less