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[QUOTE=Guest;204110]PARTHASARATHI T. R.
 Parthu_14 AT yahoo.co.in 
 
[b]Career Objective [/b]: 
- I am in the pursuit of acquiring all the competencies for a satisfying career and always willing to face new challenges and critical tasks, which offer potential growth and development through the spirit of teamwork.
[b]Organizational Experience [/b]:
- From Mar-2006 to Jan 2007 with Micro labs Ltd., as “Research Associate”, in analytical R&D department.
- From Jan-2007 to Apr 2011 with Suven Life Sciences Ltd., as “Research Associate”, in Bioanalytical department.
- From May 2011 to till date as “Assistant Manager-BIOANALYTICAL”, in Bioanalytical department at Quest life sciences Chennai.
[b]Summary of skills & experience [/b]:
- 51/2 years of experience in the field of Bioanalytical using HPLC and LC-MS/MS in Bioequivalence and Bioavailability studies.
- Sound knowledge of GLP techniques. 
- Rich experience of developing and validating Bioanalytical methods as per FDA, ANVISA, EMA guidelines.
[b]Instrument exposure [/b]: 
- LC-MS/MS – MDS SCIEX (API 2000, 3000, & API 4000)
- HPLC – Shimadzu, Perkin Elmer, Agilent 1200 & Agilent 1100, Waters Alliance 2695
- SOFTWARE – Analyst versions 1.4, 1.4.1, 1.4.2 (MDS SCIEX)
- Thermo TSQ QUANTUM LC-MS/MS system - LC Quan SOFTWARE- version 2.5.6 (Thermo TSQ quantum)
[b]Job Responsibility [/b]:
[b]- Method development & Method Validation by using various extraction procedures like liquid – liquid extraction, solid phase extraction and precipitation and analysis by LC-MS/MS (MDS SCIEX [/b]: API 3000, API 4000, Thermo TSQ QUANTUM) as per current FDA guidelines.
[b]- Analysis of Clinical samples using Liquid – Liquid, Protein precipitation and Solid Phase Extraction Techniques with LC – MS/MS (MDS SCIEX [/b]: API – 3000, API – 4000) and HPLC as per GLP requirements. 
- Responsible for the development of simple, robust, cost effective, Analytical Methods for Drug/Metabolites using LC – MS/MS, HPLC Techniques in Biological matrices.
- Review of Method SOP’S and Laboratory SOP’S as per the need.
- Review of method validation and analytical reports.
- Development and maintaining many successful efforts for GLP compliance in Bio-analytical laboratory.
- Documentation procedures as per departmental standard operating procedures (SOPs) and regulatory guidelines.
[b]Achievements [/b]:
[b]- Method development and validation for [/b]: Sibutramine, Haloperidol, Melperone, raclopride, Sitagliptin, Felodipine, aspirin and salicylic acid, sarpogrelate Simultaneous estimation for various NCE’s.
- BE studies for Trandolapril, Aspirin & Salicylic acid, Fluvastatin, Enalapril, Atorvastatin and metabolites , Fexofenadine, Diclofenac sodium, cetrizine, olanzepine, Loratadine&Desloratadine, Sirolimus, Everolimus, Furosemide. Levocetrizine, Tolterodine&metabolite, Tramadol, Carvedilol and metabolite, Zolpidem, Lepatinib, Montelukast, propranalol, Tacrolimus, Montelukast
- Invivo brain distribution studies of various NCE’s.
[b]Educational Qualification [/b]:
- Maters in Pharmacy in “Pharmaceutical Analysis” from Dr. MGR Medical University, Chennai in 2006.
- Bachelors in Pharmacy from Dr. MGR Medical University, Chennai in 2002.
[b]Papers published & presented [/b]:
[b]- Liquid chromatography tandem mass spectrometry method for the quantification of sarpogrelate, a selective 5HT2A receptor antagonist in plasma  [/b]: application to preclinical pharmacokinetic study – paper published in journal – Biomedical chromatography 
- Simultaneous extraction of acetyl salicylic acid and salicylic acid from human plasma and simultaneous estimation by liquid chromatography and atmospheric pressure chemical ionization/ tandem mass spectrometry detection – paper published in Arzneimittel forschung (Drug research) 
- Analytical method development and validation of ciprofloxacin and ornidazole in tablet dosage form by RP-HPLC Method. (57th Indian Pharmaceutical congress, Hyderabad-poster presentation)
- Analytical method development and validation of Levofloxacin and ornidazole in tablet dosage form by RP-HPLC Method. (61st Indian Pharmaceutical congress,Ahmedabad-poster presentation)
- Simultaneous determination of aspirin, clopidogrel bisulphate and atorvastatin calcium in capsule dosage form by RP-HPLC. (3rd World congress on Bioavailability & Bioequivalence- poster presentation)
[b]Audits faced [/b]:
- NABL audit three times while working in suven life sciences Ltd.
- More than 20 client audits while working in suven life sciences Ltd.
- 15 client audits in Quest life sciences pvt Ltd.
- FDA audit on clinical study of Exemestane, Temozolamide[/QUOTE]

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