Curriculum vitae

Hiren D. ShahM.Pharm – Pharmaceutical Chemistry

E-302, Sahaj Sapience.,Opp. APMC Market,Behind Vishala Hotel,Near Vaishali Township.Vasna, Ahmedabad–380 055Dist-Ahmedabad, Gujarat, INDIAContact no.: +91 9428386906Email :hirenshah2986@yahoo.co.in

Career Objective:

To assist group leader to ensure the regulatory compliance during API development (including post approval activities) and ensure compliance of regulatory requirements during life cycle and timely as well as qualitative DMF submission in global regulatory market.

To ensure compliance of regulatory requirements, in house quality system and ICH guidelines in analytical development, MCD and API PP.

Research Experience: Currently working as SCIENTIST - II in Quality department (RA and CQA) of

Torrent Reserch Centre,Ahmedabad, Previously worked as Research Associate-I in Piramal Discovery Solution Pvt.

Ltd. Ahmadabad.

Industrial Work Experience:

6.0 years rich experience in Pharmaceutical industry as well as CRO. To review Feasibility,Optimization, and RC1e study of Development chemistry. To review optimization data and process validation report and BMR of API Pilot

Plant To review Technology Transfer documents like MFC,PDR,IPS,Specification and STPs

of KSM,Raw material,Intermediate,API including Release of all specification, BOM and Master Recipe in SAP and also handing SAP

related activities like Batch Manufacturing, Batch Released COA etc. To review Protocol and report related to Method validation, Method equivalency

and Method verification and Method transfer. To review of documents and relevant raw data of references standard/working

standard, characterisation include elemental analysis of 1H NMR, 13C NMR, IR, Mass, XRPD, Chromatogram, LC MS.

Qualification documents of Equipment and Instruments,Log books as well experimental data and Lab journal of MCD etc.

To review manufacturing documents like MFC,BMR,Process validation Protocol and report,Stability protocol and report, Sampling protocol and stability data compilation.

To review and evaluate the documents,facilitates its usage for commercial purpose of API/KSM/Intermediates.

To review Change controls, Deviation, Incident and Risk Assessment. To check the system compliance of MCD and API Pilot Plant and assist in system

audit like SOPs review, log books and Journals To compile DMF and its submission as per regulatory requirement of Particular

country. Also eCTD publication through software. To evaluate queries raised by regulatory authority/Customer and prepare draft

response. To review Deviations, RAF, Incident, CCF, PVP,PVR and CAPA etc. To maintain life cycle management of product through variationAnnual report and

renewal/Re-registration submissions. To send DMF/amendments/supplements to counterparts in respective contries. To review out source DMF for all market such as US,EU,Brazil,ROW etc. To compile amendments,annual reorts,DMF/CEP as per regulatory guide line and

take care of DMF extension. To evaluate change notification/and its impact for all market. To communicate with vendor for API related issues for outsource DMF. Planned small scale batches i.e. mg, gm, & scale-up with the help of literature. Expertise of Journal Writing and Documentation as per the Clients’ requirements. Knowledge on cyanation reactions using KCN,NaCN, &CuCN and also aware of

hazardous nature of these reagents, its decomposition process. Worked on various metal reagents like n-BuLi, tert-BuLi, LDA, DIBALH, NaH, LAH,

NaBH4, NaCNBH4, etc. Succesfully carried out various name reactions like Suzuki coupling, Vilsmeir-Heck

reaction, Buchwald reaction, Mistunobureaction,Grignard Reaction etc. Undertook projects, which involved the reactions like esterification, nitration,

bromination, alkylation, condensation, protection-deprotection, cyclasation, reduction, oxidation, salt formation etc.

Familiar with the drying process of different solvents like acetone, DCM, acetonitirle , THF/Diethyl ether, DMF/DMSO, EtOH/MeOH, Benzene/Toulene.

Purification techniques used;Column chromatographyFlash C.C.CrystallizationFractional distillation.High vacuum distillationUsing preparative TLC

Academic Credentials:

Course School / CollegeYear of passing Result

M. Pharm S.K.P.C.P.E.R Kherva, GanpatUniversity

2010 70%

B.Pharm S.K.P.C.P.E.RKherva, GanpatUniversity

2008 66 %

H.S.C G.H.S.E.B 2004 85 %

S.S.C G.S.E.B 2002 88 %

Technical Skills:DMF Review and Submission: Review In House and out source DMF and submission of DMF via CESP,Eudralink and eCTD.Query response and Variation filing for regulated market.

Computer Skills: Includes Microsoft Office; Adobe Photoshop,Corel Draw; System maintenance; Software installations; Internet browsing, Drug designing softwares like CHEMDRAW, CHEMSKETCH,CHEMOFFICE,CESP,Eudralink and eCTD etc.

References:

Dr.Anil Patel Senior Scientist, Piramal Discovery Solution, Ahmedabad

Contact No. 9925206580 Declaration:

I hereby declare that the above mentioned statements are true and correct.

Regards, Hiren D. Shah

Cell no. +91 9428386906 hirenshah2986@yahoo.co.in