Highly-motivated employee with Physically fit, mentally sharp and energetic professional with 7+ years of healthcare and 7+ year of retail experience. Skilled at communicating, organizing and solving problems to raise the stature and rankings of health care and retail facilities. Hardworking, educated and willing to go the extra mile to complete any task.
Committed job seeker with a history of meeting company needs with consistent and organized practices.
· Production planning and control for various stage like Dispensing, Blending,granulation,compression,coating,capsulation,Inspection and packaging stage as per requirement.· In process checking & process Validation during various stage of processing.
· Visual inspection of finished bulk product
· Collect samples for various stage of manufacturing and Packaging as per requirement.
· Preparation, review and release of Batch Manufacturing Record.
· Maintain and perform annual visual inspection of retain and stability samples
· Perform activities related to receipt, storage, inspection, and issuance of labeling components.
· Receiving, Release and Inventory Control of packaging component like cartons and labeling.
· To verify label content, control of label and carton inventory, releasing of packaging components for packaging.
· Preparation, review and revise and implementation of SOPs.
· Reviewed documents like maintenance and calibration records, Cleaning records, Temperature and RH record, complaint records, CAPAs, GMP and quality system issue.
Handling of OOS,OOT,deviation,CAPA,Investigation report
· To co-ordinate with Q.A., Q.C. & Engineering department for related issues.
· To check the production quantitative/Qualitative output day to day basic of the machine.
· To prepare Daily, weekly and monthly report
· Record keeping as per WHO-GMP norms and FDCA requirement.
· To analyze process abnormality, problem & implementation for the same.
· To operate the plant as per the standard operating procedure and instruction of shift in charge.
· To meet the production target in shift and controlling the product specification.
· To co-ordinate with stores of issue of RM/PM materials & F & D or Q.C. for new product trial.
· To maintain & control of clean room environment.
· Preparation, review and implementation of SOPs.
· Prepare and perform the URS,DQ,IQ,OQ,PQ of various equipments in the manufacturing area.
· Area Qualification.
I here by inform that the above given information is to the best of my knowledge. I assure you of my full dedication and co-operation with you on any issue.
Thanking you for your co-operation .
Yours sincerely,
Rakeshkumar D.Patel