Mihir Ranjan Debnath1977

RESUME MR.MIHIR RANJAN DEBNATH B.PHARM PRESENT ADDRESS Mr M.R.Debnath. Sai Mahal,Flat no. 120,E wing,Sai Nagar, Sai Nagar,Palghar.Maharashtra ,

PERMANENT ADDRESS Mr. Mihir Ranjan Debnath. C/O Sudhir Debnath. Sudhir Sindhu Niwas Sarodapolly,Alipurduar. Jalpaiguri, (W.B)

Total Experience:

4 years n 09months

Current Location:

Palghar

Availability

:

Within a month

PERSONAL BRIEF Date of Birth Marital Status E-mail Address Contact No. Gender CTC

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ECTC

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27th Feb. 1977. Married. [email protected] 09823939134 Male 3.02 lac/annum. Nagotiable

Educational Qualifications: B.Pharm from Rajiv Gandhi University of Health Sciences, Bangalore in 2004 obtaining 59.83% S.S.C. in _1996________year from W..B. B_S.E(Kolkata)___Board obtaining 65% H.S.C. IN _1998_______year from _W.B.C.H.E(Kolkata)___Board obtaining 54%

JOB EXPERIENCE/ JOB DESCRIPTION Professional Experiemce:4 years n 09 months Project # 1 Organization : Designation : Duration

Famy Care Ltd. Production Chemist December 2003 to December 2004

Responsibilities:1.To look after the production(Granulation,Compression,Coating),To fillup the B.M.R,Log sheet,Daily:s documentation like cleaning record. 2.reconciliation of batches. 3.to record the recovery 4.cleaning record of Equipments. Project # 2 Organization : Aristo Pharmaceuticals Ltd( Mapra Labs Pvt Ltd.) Designation : Sr. Production Chemist Duration December 2004 to February 2007 Responsibilities:1.To look after the whole production mentioned above. 2 to prepare the A.P.R(Annual product review). 3To prepare the W.H.O documentations. 4.To prepare n revise the B.M.R,B.P.R n other relevents documents. Project # 3 Organization Designation Duration

: Macleods Pharmaceuticals Ltd. : Executive production :Feb”07 to till now

Responsibilities:1To look after the Whole production. 2.to prepare n issue the B.M.R,B.P.R. 3.Other relevents documents concern with production. 4W.H.O,cGMP protocol. Technical Skills: #1.preparation of schedule and procedure of periodic training of the employees. #2.Preparation of Annual product Quality Review #3.Preparation and revise in process related SOPs.

#4.Calibration of the Equipments and Instruments. #5.Validation concern with process. #6.Preparation of Cleaning method of Validation #7.Monitoring and improvement of yields and recoveries,monitoring quality aspect. #8.Inter departmental follow ups with quality control,Quality Assurance,dispensing n maintenance. Career Objective:I am looking forward a suitable position in Production.I expect a career which is different but yet unique,My intelligence is continuously nourished by challenges n constant quest for advanced knowledge nnewest one of technologies so that I can achieve extra ordinary knowledge.

Summary: Having knowledge in tablet, capsule and oral liquid and Their filling and Packing alongwith fillingup relevant documents like WHO,cGMP,required documents,to look after the whole production,preparing planning n production output with co-ordination with the other production concern personnels. EXTRA CURRICULUM VITAE :Having knowledge in basic Computer,Internet.

DESCRIPTION ABOUT PLANT : W.H.O, UNFPA and GMP Approved. AUDITS FACE :W.H.O-GMP,UNFPA,India-GMP(FDA),Audit of Tangenia,Kenya,Uganda,Russia Etc I hereby declare that the above mentioned information is true to the best of my knowledge. PLACE:-Palghar,Maharashtra DATE:-29-08-2008 (MIHIR RANJAN DEBNATH)