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NAGA MALLIKARJUNARAJA B
8-2-89, Sastry Nagar, Badvel (P & M), Kadapa District, Andhra Pradesh – 516227
Contact: +91 9052161020; Email: arjunbale@gmail.com
A systematic, organized, hardworking and dedicated team player with an analytical bent of mind with
excellent academic credentials. I am a qualified individual with M. Pharma (Pharmaceutical Analysis &
Quality Assurance) from Raghavendra Institute of Pharmaceutical Education and Research,
Anantapuramu; accented with the latest trends and techniques of the field.
Possess keen interest in the area of Analysis and Quality Assurance with expertise in handling sophisticated
analytical instruments like T.L.C., Spectrophotometer, HPLC, LC-MS, GC, FTIR, FTIR-ATR, UV, and pH
Meter.
A hard working & talented individual seeking a challenging job that would synergize my skills and
knowledge with the objectives of the organization, a responsible, reliable and committed worker, give my
best both as a part of a team and working independently.
The above credentials along with my enclosed resume make me ideally suitable for a position in your
organization. I would appreciate an opportunity for a personal interview.
Thanking you,
Yours sincerely
Naga Mallikarjuna Raja B
NAGA MALLIKARJUNARAJA B
8-2-89, Sastry Nagar, Badvel (P & M), Kadapa District, Andhra Pradesh – 516227
Contact: +91 9052161020; Email: arjunbale@gmail.com
RESEARCH CHEMIST
Seeking a position in the Pharmaceutical industry that provides me ample opportunity to explore & excel
while carving out the niche for personal, professional as well as organizational goals
Work Experience
 Currently working as Research Chemist in Analytical Research and Development department of SAI
Life Sciences Limited, Hyderabad
 Previously worked as Trainee Scientist in Bioanalytical department of Manipal AcuNova Limited,
Manipal from 24-Mar-2014 to 20-Dec-2014
Profile
 Qualified M. Pharma (Pharmaceutical Analysis & Quality Assurance) from Raghavendra Institute of
Pharmaceutical Education and Research, Anantapuramu; accented with the latest trends and techniques
of the field, determined to carve a niche in the industry
 Good knowledge across various therapeutic areas like tablet/capsule and liquid orals. Expertise in
handling sophisticated analytical instruments like T.L.C., Spectrophotometer, HPLC, FTIR, FTIR-AR,
UV, Column Chromatography , Tablet dissolution apparatus and PH Meter
 Academically astute secured AIR-3167 in GPAT-2011. Understanding of Formulation and Development
(F&D), Drug Regulatory Affairs (DRA), Intellectual Property Rights (IPR), Quality Assurance (QA),
Regulatory Affairs and Quality Control
 Having knowledge in quality assurance domain including all fine aspects like Qualifications & Process
Validations, Analytical Method Development, In-Process Quality Assurance and Instrumental Analysis
 Good Knowledge on Manuscript writing and Abstract writing, conceptually strong with an innovative
and analytical approach to the work with an eye for detail
Job Summary
 Currently Working as Research Chemist in SAI Life Sciences Limited, Hyderabad, since 23rd
December 2014 to till date, includes Method Development, Validation, Calibration of analytical
instruments, HPLC Column Performance and reaction monitoring support to PR&D
 To perform Method development of NCE (New Chemical Entity) & API molecules by HPLC
 To develop cost effective method validations according to the current ICH guidelines and regulatory
requirements in stricter to GLP compliant laboratory
 Calibration of Analytical Equipments as and when required
 Expertise in maintaining highest level of quality in operations and adhere to all the quality parameters
and procedures as per the stringent norms
 Preparation of method of analysis, Standard Test Procedure, Specifications and COA’s
 Performing analysis for Finished Products, Intermediates and raw materials
 Coordinating with Process Chemistry and other departments for timely completion of assigned
projects
 Strict adherence to all the relevant standard operating procedures and compliance to all the GLP,
GDP and Safety precautions in laboratory
Instruments Handled
 HPLC (Alliance 2695), UPLC (Acquity H Class) of Waters (Empower3)
 RRLC 1200 series of Agilent (Ezchrome Elite)
 LC 2010C HT and LC Prominence of Shimadzu (LC Solutions)
 THERMO SCIENTIFIC LC-MS/MS Discovery Max and Ultra (LC Quan)
 BRUKER FT-IR (Alpha) and ATR, Pellet (Opus)
 UV Spectrophotometer (Jasco)
EDUCATIONAL CREDENTIALS
M. Pharma (Pharmaceutical Analysis & Quality Assurance), 2013
Raghavendra Institute of Pharmaceutical Education and Research, Anantapuramu, Distinction
B. Pharma, 2011
Vagdevi College of Pharmacy & Research Centre, Nellore
12th, 2006
Venus Junior College, Guntur
10th, 2004
Kiran English Medium High School, Tirupati
Computer Proficiency
MS Office, Windows and Internet Applications
Academic Projects Undertaken
 Stability Indicating RP- HPLC Method for Determination of Flupiritine maleate in Pharmaceutical Dosage
Forms and Characterization of Hydrolytic Products (Major Project during M. Pharma)
 Phytochemical analysis of Chloroform Extract of Wrightia tinctoria leaf by Modern Analytical techniques
 Formulation of Tinidazole Liquisolid Tablet and Invitro Evaluation (During B. Pharma)
Research Publications
 P Muthu Kumaran*, N Saraswathy, B Naga Mallikarjuna Raja, A Pravalika, "Anti-arthritic and
antioxidant activity of aqueous and Ethanolic extracts of Adenanthera Pavonina leaves", Inventi Rapid:
Planta Activa, Vol. 2013, Article ID - "Inventi:ppa/232/13", 2013
 Ramalingam P, Naga Mallikarjuna Raja B* Sasikala M and Krishna Karthik P.; RP-HPLC “Method
development and validation for the Quantization of Pioglitazone in cleaning validation”; Inventi Rapid:
Pharma Analysis & Quality Assurance, (2013); (2): 1-4
 M. Sasikala*, M. Teja Deepthi, K. Vinod Kumar and Naga Mallikarjuna Raja B.; “Development and
Validation of UV Spectrophotometric method for Simultaneous Estimation of Tenofovir Disproxil
Fumerate and Emtricitabine in Tablet Dosage Form by Derivative Spectroscopic Method”; International
Bulletin of Drug Research., 3(5): 20-28, 2013
 Ramalingam Peraman*, KV Lalitha, Naga Mallikarjuna Raja B and Hari Babu Routhu; “Identification of
Degradation Products and Stability-Indicating RP-HPLC Method for Determination of Flupirtine maleate
in Pharmaceutical Dosage Forms”; Sci Pharm; in press.doi:10.3797/scipharm.1310-01
Date of Birth: 18th June, 1989
Languages Known: English, Telugu, Hindi and Kannada

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CV _ AR&D II

  • 1. NAGA MALLIKARJUNARAJA B 8-2-89, Sastry Nagar, Badvel (P & M), Kadapa District, Andhra Pradesh – 516227 Contact: +91 9052161020; Email: arjunbale@gmail.com A systematic, organized, hardworking and dedicated team player with an analytical bent of mind with excellent academic credentials. I am a qualified individual with M. Pharma (Pharmaceutical Analysis & Quality Assurance) from Raghavendra Institute of Pharmaceutical Education and Research, Anantapuramu; accented with the latest trends and techniques of the field. Possess keen interest in the area of Analysis and Quality Assurance with expertise in handling sophisticated analytical instruments like T.L.C., Spectrophotometer, HPLC, LC-MS, GC, FTIR, FTIR-ATR, UV, and pH Meter. A hard working & talented individual seeking a challenging job that would synergize my skills and knowledge with the objectives of the organization, a responsible, reliable and committed worker, give my best both as a part of a team and working independently. The above credentials along with my enclosed resume make me ideally suitable for a position in your organization. I would appreciate an opportunity for a personal interview. Thanking you, Yours sincerely Naga Mallikarjuna Raja B
  • 2. NAGA MALLIKARJUNARAJA B 8-2-89, Sastry Nagar, Badvel (P & M), Kadapa District, Andhra Pradesh – 516227 Contact: +91 9052161020; Email: arjunbale@gmail.com RESEARCH CHEMIST Seeking a position in the Pharmaceutical industry that provides me ample opportunity to explore & excel while carving out the niche for personal, professional as well as organizational goals Work Experience  Currently working as Research Chemist in Analytical Research and Development department of SAI Life Sciences Limited, Hyderabad  Previously worked as Trainee Scientist in Bioanalytical department of Manipal AcuNova Limited, Manipal from 24-Mar-2014 to 20-Dec-2014 Profile  Qualified M. Pharma (Pharmaceutical Analysis & Quality Assurance) from Raghavendra Institute of Pharmaceutical Education and Research, Anantapuramu; accented with the latest trends and techniques of the field, determined to carve a niche in the industry  Good knowledge across various therapeutic areas like tablet/capsule and liquid orals. Expertise in handling sophisticated analytical instruments like T.L.C., Spectrophotometer, HPLC, FTIR, FTIR-AR, UV, Column Chromatography , Tablet dissolution apparatus and PH Meter  Academically astute secured AIR-3167 in GPAT-2011. Understanding of Formulation and Development (F&D), Drug Regulatory Affairs (DRA), Intellectual Property Rights (IPR), Quality Assurance (QA), Regulatory Affairs and Quality Control  Having knowledge in quality assurance domain including all fine aspects like Qualifications & Process Validations, Analytical Method Development, In-Process Quality Assurance and Instrumental Analysis  Good Knowledge on Manuscript writing and Abstract writing, conceptually strong with an innovative and analytical approach to the work with an eye for detail Job Summary  Currently Working as Research Chemist in SAI Life Sciences Limited, Hyderabad, since 23rd December 2014 to till date, includes Method Development, Validation, Calibration of analytical instruments, HPLC Column Performance and reaction monitoring support to PR&D  To perform Method development of NCE (New Chemical Entity) & API molecules by HPLC  To develop cost effective method validations according to the current ICH guidelines and regulatory requirements in stricter to GLP compliant laboratory  Calibration of Analytical Equipments as and when required  Expertise in maintaining highest level of quality in operations and adhere to all the quality parameters and procedures as per the stringent norms  Preparation of method of analysis, Standard Test Procedure, Specifications and COA’s  Performing analysis for Finished Products, Intermediates and raw materials  Coordinating with Process Chemistry and other departments for timely completion of assigned projects  Strict adherence to all the relevant standard operating procedures and compliance to all the GLP, GDP and Safety precautions in laboratory
  • 3. Instruments Handled  HPLC (Alliance 2695), UPLC (Acquity H Class) of Waters (Empower3)  RRLC 1200 series of Agilent (Ezchrome Elite)  LC 2010C HT and LC Prominence of Shimadzu (LC Solutions)  THERMO SCIENTIFIC LC-MS/MS Discovery Max and Ultra (LC Quan)  BRUKER FT-IR (Alpha) and ATR, Pellet (Opus)  UV Spectrophotometer (Jasco) EDUCATIONAL CREDENTIALS M. Pharma (Pharmaceutical Analysis & Quality Assurance), 2013 Raghavendra Institute of Pharmaceutical Education and Research, Anantapuramu, Distinction B. Pharma, 2011 Vagdevi College of Pharmacy & Research Centre, Nellore 12th, 2006 Venus Junior College, Guntur 10th, 2004 Kiran English Medium High School, Tirupati Computer Proficiency MS Office, Windows and Internet Applications Academic Projects Undertaken  Stability Indicating RP- HPLC Method for Determination of Flupiritine maleate in Pharmaceutical Dosage Forms and Characterization of Hydrolytic Products (Major Project during M. Pharma)  Phytochemical analysis of Chloroform Extract of Wrightia tinctoria leaf by Modern Analytical techniques  Formulation of Tinidazole Liquisolid Tablet and Invitro Evaluation (During B. Pharma) Research Publications  P Muthu Kumaran*, N Saraswathy, B Naga Mallikarjuna Raja, A Pravalika, "Anti-arthritic and antioxidant activity of aqueous and Ethanolic extracts of Adenanthera Pavonina leaves", Inventi Rapid: Planta Activa, Vol. 2013, Article ID - "Inventi:ppa/232/13", 2013  Ramalingam P, Naga Mallikarjuna Raja B* Sasikala M and Krishna Karthik P.; RP-HPLC “Method development and validation for the Quantization of Pioglitazone in cleaning validation”; Inventi Rapid: Pharma Analysis & Quality Assurance, (2013); (2): 1-4  M. Sasikala*, M. Teja Deepthi, K. Vinod Kumar and Naga Mallikarjuna Raja B.; “Development and Validation of UV Spectrophotometric method for Simultaneous Estimation of Tenofovir Disproxil Fumerate and Emtricitabine in Tablet Dosage Form by Derivative Spectroscopic Method”; International Bulletin of Drug Research., 3(5): 20-28, 2013  Ramalingam Peraman*, KV Lalitha, Naga Mallikarjuna Raja B and Hari Babu Routhu; “Identification of Degradation Products and Stability-Indicating RP-HPLC Method for Determination of Flupirtine maleate in Pharmaceutical Dosage Forms”; Sci Pharm; in press.doi:10.3797/scipharm.1310-01 Date of Birth: 18th June, 1989 Languages Known: English, Telugu, Hindi and Kannada