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MEHUL D. PATEL
Plot No. 125/1, Sector No. 4 “A”
GANDHINAGAR-382004.
Phone No. : 9925810533(M), (R ) 9978999085.
E-Mail: rxmehul@gmail.com
Prefered location for job: Banglore, Hyderabad, Pune,Mumbai.
Working as a Research Associate in Torrent Pharmacuticles Ltd. In Bio-Analytical Department since
April,2006.
Job Description:
1 To conduct (Perform & Direct) Bio-Analytical Activities(MD,MV and sample analysis) using
various applicable techniques as per approved methods/protocols and to acheive reruired
bench-mark at each stage.
2 To conduct the Bionalaytical acitvity of DMPKI(Drug metabolisum and Pharmacokinetics)activity
3 To review the standard operating test procedure/protocol(SOTP) to ensure its accuracy and
completeness.
4 To supervise scientist in planning of study requirements and day to day bio-analytical project
activity.
5 To review the raw data generated during method development ,method validation and study
sample analysis.
6 To report the critical analytical observations to seniors and conduct the investigations for CAPA
(if required).
7 To ensure the proper planning of resources like instument,column,manpower,standards etc to
meet the desired timeline.
8 To supervise,operate,maintain and perform calibration/performance check of instruments.
9 To ensure optimum utilization of LCMSMS and track non-utilization of the same.
10 To train the subordinates on technical and quality related skills.
11 To review the standard operating procedures to ensure confirmity with the regulatory
requirements.
12 To review the outsource studies in order to ensure the compliance of the respective regulatory
requirement.
13 To ensure compliance of GCP practices and HSE policies.
Publications:
A high throughput and sensitive liquid chromatography-tandem mass spectrometry (LC-MS/MS)
method for the estimation of Bisoprolol in human plasma using multiplexing technique.
Worked as Research Associate in Department of Bio-Analytical, CADILA
Pharmaceutical Ltd., Dholka, from October,2005 to March,2006 in an ANVISIA
approved Lab.
Job Description:
1 Acting as an In charge of Bio Analytical laboratory, Cadila Pharmaceutical Ltd. Dholka
14 Faced several National and International Audits (DCGI, MCC, ANVISIA)
1 Developed and validated more then 25 methods on HPLC and LC-MS/MS.
2 Able to handle instruments like LC-MS/MS (API-3000, API-4000, API-Q-TRAP), HPLC
(Shimadzu, Waters, Dionex, Borwin)
1 Able to handle various analytical software like Analyst, Class-VP, Borwin etc.
15 Developed various SOPs
16 Given training to the analysts
Academics
ü Completed M. Pharm. (Pharmacology) from K. B. institute of Pharmaceutical Education
and Research, Gandhinagar (Gujarat University) with First Class in November 2005.
ü Completed B. Pharm. from K. B. institute of Pharmaceutical Education and Research,
Gandhinagar (Gujarat University) with First Class in September 2000
Professional appointments
1. Duration : September2000-August 2003:
Organization : LAMBDA Therapeutic Research Limited,
42 Premier House I, Bodakdev, S.G. highway,
Ahmedabad. 380 054.
Designation : RESEARCH ASSOCIATE (Bioanalytical department.)
NOTE: Selection was done from Campus interview.
2. Duration : October 2005 till date.
Organization : CADILA Pharmaceutical Ltd.,
1389,Trasad Road, Dholka-387 810.
Designation : RESEARCH ASSOCIATE, Bioanalytical laboratory, CRO
NOTE: Selection was done from Campus interview.
Job responsibilities at present:
1 Overall In-Charge of Bioanalytical Laboratory
1 Method development, Method validation for various drugs estimation on LC-MS/MS
and HPLC
1 Preparation/ revision of SOPs for various functions of the Bio-analytical area
1 Analysis of Biological samples for different drug products
1 Preparation of Method SOP, Method Validation and Analytical Reports
1 Maintaining the Bio-Analytical Laboratory as per GLP compliance.
1 Responsible for calibration and maintenance of the equipments and instruments.
1 Maintenance and documentation of all the concern analysis records.
1 LC-MS/MS related spare parts and Column, indenting and up keeping record of the
same.
Conference and Workshop attended:
1. 51st
Indian Pharmaceutical Congress at Indor, December 2000.
1. 33rd
Indian Pharmacological Society at Gandhinagar, 2000.
1. Seminar on “Introduction and updates for Good Laboratory Practice” by Dr. Nigel
Dent at Ahmedabad, 7th
September 2001.
1. 36th
Indian Pharmacological Society at Delhi, 2003.
1. 37th
Indian Pharmacological Society at Kolkata, January 2005.
1. Joint International Conference (Indian Sector) at Ahmedabad, December, 2004.
1. Clinical Research from Theory to Practice. Advance module & BA/BE Studies
organized by ACE at Dholka, December 2005.
PERSONAL DETAILS:
Date of Birth: 24th
November 1978.
Marital Status: Married
Language Known: English, Hindi and Gujarati.
Nationality: India

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Mehul D. Patel's Bio-Analytical Research Experience and Skills

  • 1. MEHUL D. PATEL Plot No. 125/1, Sector No. 4 “A” GANDHINAGAR-382004. Phone No. : 9925810533(M), (R ) 9978999085. E-Mail: rxmehul@gmail.com Prefered location for job: Banglore, Hyderabad, Pune,Mumbai. Working as a Research Associate in Torrent Pharmacuticles Ltd. In Bio-Analytical Department since April,2006. Job Description: 1 To conduct (Perform & Direct) Bio-Analytical Activities(MD,MV and sample analysis) using various applicable techniques as per approved methods/protocols and to acheive reruired bench-mark at each stage. 2 To conduct the Bionalaytical acitvity of DMPKI(Drug metabolisum and Pharmacokinetics)activity 3 To review the standard operating test procedure/protocol(SOTP) to ensure its accuracy and completeness. 4 To supervise scientist in planning of study requirements and day to day bio-analytical project activity. 5 To review the raw data generated during method development ,method validation and study sample analysis. 6 To report the critical analytical observations to seniors and conduct the investigations for CAPA (if required). 7 To ensure the proper planning of resources like instument,column,manpower,standards etc to meet the desired timeline. 8 To supervise,operate,maintain and perform calibration/performance check of instruments. 9 To ensure optimum utilization of LCMSMS and track non-utilization of the same. 10 To train the subordinates on technical and quality related skills.
  • 2. 11 To review the standard operating procedures to ensure confirmity with the regulatory requirements. 12 To review the outsource studies in order to ensure the compliance of the respective regulatory requirement. 13 To ensure compliance of GCP practices and HSE policies. Publications: A high throughput and sensitive liquid chromatography-tandem mass spectrometry (LC-MS/MS) method for the estimation of Bisoprolol in human plasma using multiplexing technique. Worked as Research Associate in Department of Bio-Analytical, CADILA Pharmaceutical Ltd., Dholka, from October,2005 to March,2006 in an ANVISIA approved Lab. Job Description: 1 Acting as an In charge of Bio Analytical laboratory, Cadila Pharmaceutical Ltd. Dholka 14 Faced several National and International Audits (DCGI, MCC, ANVISIA) 1 Developed and validated more then 25 methods on HPLC and LC-MS/MS. 2 Able to handle instruments like LC-MS/MS (API-3000, API-4000, API-Q-TRAP), HPLC (Shimadzu, Waters, Dionex, Borwin) 1 Able to handle various analytical software like Analyst, Class-VP, Borwin etc. 15 Developed various SOPs 16 Given training to the analysts Academics ü Completed M. Pharm. (Pharmacology) from K. B. institute of Pharmaceutical Education and Research, Gandhinagar (Gujarat University) with First Class in November 2005. ü Completed B. Pharm. from K. B. institute of Pharmaceutical Education and Research, Gandhinagar (Gujarat University) with First Class in September 2000
  • 3. Professional appointments 1. Duration : September2000-August 2003: Organization : LAMBDA Therapeutic Research Limited, 42 Premier House I, Bodakdev, S.G. highway, Ahmedabad. 380 054. Designation : RESEARCH ASSOCIATE (Bioanalytical department.) NOTE: Selection was done from Campus interview. 2. Duration : October 2005 till date. Organization : CADILA Pharmaceutical Ltd., 1389,Trasad Road, Dholka-387 810. Designation : RESEARCH ASSOCIATE, Bioanalytical laboratory, CRO NOTE: Selection was done from Campus interview. Job responsibilities at present: 1 Overall In-Charge of Bioanalytical Laboratory 1 Method development, Method validation for various drugs estimation on LC-MS/MS and HPLC 1 Preparation/ revision of SOPs for various functions of the Bio-analytical area 1 Analysis of Biological samples for different drug products 1 Preparation of Method SOP, Method Validation and Analytical Reports 1 Maintaining the Bio-Analytical Laboratory as per GLP compliance. 1 Responsible for calibration and maintenance of the equipments and instruments. 1 Maintenance and documentation of all the concern analysis records. 1 LC-MS/MS related spare parts and Column, indenting and up keeping record of the same.
  • 4. Conference and Workshop attended: 1. 51st Indian Pharmaceutical Congress at Indor, December 2000. 1. 33rd Indian Pharmacological Society at Gandhinagar, 2000. 1. Seminar on “Introduction and updates for Good Laboratory Practice” by Dr. Nigel Dent at Ahmedabad, 7th September 2001. 1. 36th Indian Pharmacological Society at Delhi, 2003. 1. 37th Indian Pharmacological Society at Kolkata, January 2005. 1. Joint International Conference (Indian Sector) at Ahmedabad, December, 2004. 1. Clinical Research from Theory to Practice. Advance module & BA/BE Studies organized by ACE at Dholka, December 2005. PERSONAL DETAILS: Date of Birth: 24th November 1978. Marital Status: Married Language Known: English, Hindi and Gujarati. Nationality: India