Manager Assistant

MAHENDRA V. BHUVA

A-***,Harsh platinum III Nr.Iscon flower, Ghuma Shella road Bopal-Ghuma Ahmedabad(Gujarat) *******@*****.**.** M) 094********

To,

RESPECTED SIR,

I am currently working as Research scientist (Assistant manager) in ADL Department in Astron Research,Intas Pharmaceuticals, Ahmedabad from October 2015 till now.

I Recently Worked in ADL Department (ANDA) in Torrent Research centre, Ahmedabad.

I completed my M.Sc. in Material science From Sardar patel University, Vallabh vidyanagar.

I am looking forward for a better prospect, to achieve great height in Pharmaceutical Company, Excellent R&D, Quality Assurance based on a dedication, loyalty and ethic.

Here with I enclose my CV for your kind perusal. I hope you will consider my CV and provide me an opportunity to work in your Company. I will do the work with great responsibility and will make positive contribution in position you offer.

A waiting an early and favorable response from your organization.

Thanking you

Yours sincerely

(Mahendra Bhuva)

Curriculum Vitae

MAHENDRA V. BHUVA

Email: *******@*****.**.** Address : A -601,Harsh platinum III

. Nr.Iscon flower

. Ghuma-Shella road

Bopal-Ghuma

Ahmedabad(Gujarat)

*******@*****.**.**

M) 094********

Objective

To Pursue a challenging career in Pharma sector by utilizing and enhancing my skills and work in an environment that provides me a challenging edge to sharpen my skills and to contribute constructively to the organization.

Ever positive never negative attitude.

Academic Qualification

Academic Qualification

Institute/ University

Year of Passing

% OBTAINED

M.Sc

Sardar patel University

2004

59.5%

B.Sc

Sardar patel University

2002

55.27 %

Other Computer Proficiency

Ms Office 2003 & 2007, Windows 98, XP & 7, E –Mail & Internet.

Basic Knowledge Of Computer, MS-Office.

Work Experience

Total Experince:-14 Years

1) I am currently working ADL Department(US &E.U Market) in Astron Research,Intas Pharmaceuticals, Ahmedabad.

Designation : Working as Research Scientist (Assistant Manager) in ADL – F & D for (Regulatory) i.e. Europe, US, Brazil, Canada etc. markets From 19th October 2015 till date.

2) My Previous Organization I worked for was Torrent Pharmaceutical Ltd. (Research Centre) – Bhat – Gandhinagar /Ahmedabad, Gujarat.

Designation : Worked as Scientist-II in Analytical Research And Development – Generics Formulation & API combined for PDG-V i.e. Europe, US, Brazil, Heumann (Germany) etc. markets From 25th September 2006 to 17th Octomber 2015.

3) My Previous Organization I Worked for was Gujarat Agrochem LTD, Panoli, Ankleshwar, Gujarat.

Designation : Worked as Q.C.Officer in Quality Control/Analytical Development etc.From June 2004 to September 2006.

Job Profile

In My Current Organization in Analytical Research and development (ADL) Job profile as below:

Planing and Review of Developing And Validation of Chromatographic Methods for RS, Assay, etc. for Solid Oral dosage forms, parentals, Injectables, suspension, gel.

Prepared and review as when required of Method validation Report & Protocol and also Technology Transfer documents & queries

Optimization batches studies, preparation of STP, MOA, COA, Stability Report, Development Report,

Calibration of different instruments like HPLC, Dissolution Apparatus, instruments used for Chemical analysis

Maintain GLP Compliance in Lab.

Job Summary : Previous Organizations(TRC)

Developing and Validating Chromatographic Methods for RS, Assay, Dissolution, BU, CU, Cleaning, Swabbing etc. for various dosage forms like Tablets, Capsules, as well as Stability indicating Methods for different API, Intermediates, Stages, KSM And Active contribution for various activities in supporting work in a Group.

Partial method validation. Development, Optimization batches studies, preparation of STP, MOA, COA, Stability Report, Development Report

Calibration of different instruments like HPLC, Dissolution Apparatus, instruments used for Chemical analysis

Maintain GLP Compliance.

MAJOR TASKS / ASSIGNMENT HANDLED

At TRC (PDG-V) ADL Formulation+API my Active contribution in following Steps Developed HPLC Methods for RI, Assay, Dissolution, BU, CU, TLC, Swabbing and also Dissolution by UV method for Different Dosage forms or Drug products.

Developed HPLC Methods for RI, Assay method for Different Drug Substances, KSM, Stages, & Intermediates.Developed Mass Methods for Genotoxic Impurity in US – FDA Queries

Chiral Analysis – Normal Phase as well as Reverse Phase.

RS-WRS Qualification – Maintains analytical data & analysis for the same.

Documentation Preparation of SOP, MOA, COA, Stability Reports, etc.

Projects Handled Mainly for Europe, US Market Projects Handled Mainly for Heumann (i.e.Germany) like, Rivastigmine API & Caps (2.5,5,10,20mg Capsules),Ramipril, Ramipril+HCTZ and many more Projects handled for Heumann Countries.

Post Dossiers Queries Solved & Regulatory Compliance Related work done for US,Europe Market as and when required as well as Heumann (germany) Projects.

Technology Transferred for Products i.e. Olmesartan Medoxomil+Amlodipine Tabs, Olme Medoxomil + Hydrochlorothiazide Tabs with In-house & Secondary API source,Pregabalin Caps, Quetiapine Fumarate API, IR, SR Tabs to QC Successfully with & Exhibit Batch Study with In-house & Secondary API source also.

Active contribution for other various activities in supporting work in a Group.

Development achievement for the RI/Assay/Dissolution Short methods for API as well as Formulations with RRLC/HPLC as well as successfully those methods are Validated & technology transferred to the QC successfully.

ASSIGNMENTS/ACHIVEMENTS &SKILLS:

Mainly worked in Dosage Forms like Tablets, Combination products i.e. Tablets, Capsules.

Tablets : Immediate/Extended/Controlled/Delayed Release Tablets, Dispersible Tablets, Mouth Dissolving Tablets & Film Coated Tablets.

Capsules : Immediate Release Capsules & MR pellets also.

Suspensions : Ready Mix, Dry Powders for Suspensions (Dry Suspensions)

Literature Skills: Reference Drug Molecule / Product Related Information from Published and Un-Published Data.

Regulatory Skills : Patent Surfing and Reading, Patent Report Study.

Trouble Monitoring for Existing Drug Substances and Drug Products

Seminar Attended

Waters – HPLC (Empower software as well as Waters - Column Chemistry)

Waters – UPLC, Agillent – RRLC (Software as well as Column Chemistry)

Shimadzu LC Solution 21-CFR Compliance & Class-VP Software etc.

DSC, TGA, DTA, Metrohm – Autotitrator, diiferent types of KF, Rhometer, & also for Milli-Q Water etc. having awareness of the applications of all.

HPLC Waters Neugenesis Data Trasfer & SMS software.

Compliance with ICH, CGLP, FDA US, Eu, & Other Regulatory guidelines, HPLC & Dissolution Method Developments.

Impurity Profiling, Impurity Characterization, Genotoxic impurities, Quality affairs, Regulatory affairs, Basic Life supports, Polymorphism, IPR, Safety, Certified Training Programme on first aid only.

Strength & virtues

Operate DISSOLUTION Apparatus, HPLC, UPLC, U.V, KARL FISHER,AAS Apparatus

Operate HPLC of Waters, Agillent Technology, Shimadzu, Perkin Elmer

Analytical Method Validation

Having a Knowledge of Bioanalytical method development and analysis of biological samples…

High innovative and creative thinking.

Excited by the challenge of research and experiment.

Willingness to learn and accept challenges.

Strong determination towards any given.

Personal Information

‘My only aim in life is to make my family and the company at which I work keep smiling and to make them at the top most level’

Date of Birth

1st December 1980

Father’s Name

Mr. valjibhai bhuva

Gender

Male

Nationality

Indian

Language known

English, Hindi and Gujarati

AREA OF INTEREST

ADL, Analytical Method Development, Analytical Method Validation, Quality Assurance, Research and Development, Bio analytical Laboratory and Quality Control.

Hobbies

Listening music & reading books.

Outsourcing

Cricket

Personnel skill

Comprehensive Problem Solving.

Willingness to learn new ideas.

Research Work.

Strong motivation power.

Good communication Power.

References

01) Mr. Atul sharma 03)Mr. Jasvant kavia

AGM, Analytical Department AGM,Astron Research

Torrent Research center, Ahmedabad Intas pharmaceutical Ltd.

Declaration: - I hereby declare that the given above information is true to best of my knowledge.

Place: Ahmedabad

MAHENDRA V. BHUVA

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