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[QUOTE=Unregistered;295077]CURRICULUM VITAE
D.RAGHAVENDRA RAO
[b][u]E-Mail [/u][/b]:raghu1980sainath AT gmail.com

[b][u]Objective  [/u][/b]:
Being a firm believer of the fact “Quality always notches an elevation of one degree in terms of productivity and profitability’’. I want to be responsible for the Quality Control Management at every step of product manufacturing and processing

[b][u]Experience Summary [/u][/b]:
** Working in Quality Control Department as Analyst in Divi’s Laboratories from april-2009 to till date. It is a manufacturing unit of Active Pharmaceutical ingredient’s (Plant is Having Approval of USFDA and TGA).
** Good exposure to the Instruments used in Quality Control
** Excellent Communication and Inter-Personal skills.

[b][u]Handling of Instruments [/u][/b]:
** KF Autotitrator, coulourimeter, Polarimeter, potentiometer titrations by Autotitrator MR Apparatus.
** Handling of HPLC Shimadzu-2010 (LC Solutions),GC Shimadzu 2014,2010,Perkinelmer Clarus 500, Agilent-7820A(GC Solution & Open lab)
** Being involved in regular analysis (Raw Material, Intermediates, Final/Finished and Stability samples).
** Reporting of results obtained during regular and stability analysis with the help of LIMS (Laboratory Information Management System).

[b][u]Educational Qualifications [/u][/b]:
** M Pharmacy (Pharmaceutical Analysis) with [67%] in National College of pharmacy shivamoga, affiliated to RGUHS Bangalore [2006-2008].
** B Pharmacy with [62%] in VL College of Pharmacy ,Raichur, affiliated to RGUHS Bangalore (2000-2004)

[b][u]Job Responsibilities [/u][/b]:
** Complete Analysis of Finish Product, Intermediate sample & Raw materials.
** Analysis of Related substances by HPLC, Assay by HPLC, GC purity, Assay by GC and Residual Solvents by GC- Head space and Injection technique.
** Analysis of Stability Samples by HPLC and GC.
** Reviewing and processing data. Interpreting test results and ensuring that they meet specification, entering data into the computer, maintaining instrument logbooks, laboratory worksheets and all relevant documentation according to cGMP documentation practices, and reviewing all information and compiling information into report form.
** Upgrading the various procedures and carrying out special tests by developing the test procedures as per customer request.
** To carry out the calibration as per schedule and troubleshooting of the instruments
** To carryout the laboratory investigation in case of any out of specification results, Non conformities, Deviation of results.
** Handling Complaint and customer feedbacks
** Validation of chromatography methods(ICH)
** Qualification of instruments
** Method development for Gas chromatography techniques.
** Carrying out Quality risk management task for Analytical methods.
** Inventory management of Chemicals / Solvents, Glassware, Spares, Consumables and Stationery.
** Familiar with Quality systems such as Change control, Deviations, CAPA.

[b][u]Personal Particulars [/u][/b]:
 [b][u]Name  [/u][/b]: D.Raghavendra Rao
 [b][u]Father’s Name  [/u][/b]: D.Balakrishna Rao
 [b][u]Gender  [/u][/b]: Male
 [b][u]Nationality  [/u][/b]: Indian
 [b][u]Marital Status  [/u][/b]: Single
 [b][u]Date of Birth  [/u][/b]: 10th Aug 1980
 [b][u]Languages Known  [/u][/b]: English, Telugu, Hindi Kannada.

[b][u]Declaration [/u][/b]:
I hereby declare that the above-furnished information is true and correct to the best of my knowledge and belief.
 [b][u]Place [/u][/b]: Vishakapatnam. 
[b][u]Date [/u][/b]: 
(D.RAGHAVENDRA RAO)[/QUOTE]

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