CURRICULUM VITAE

Name:- Mr.Mahesh.A.Bhandare

Address:- 202 Bharat Sadan,S.V.Road

Behind Saraswati Secondary School Marathi Medium

,Naupada,Thane(W) - 400 602.

Ph:- Ph 998-***-****,

Age :- 55 years.

EDUCATIONAL QUALIFICATIONS

Exams Passed

Year of passing

Board/University

Class/Grade

S.S.C

1982

Pune Div Board

Ist Class

H.S.C

1985

Pune Div Board

Pass

B.Sc

1988

Mumbai University

II nd

D.I.A.C

1989

Ruia College

“C”grade

M.Sc(Analytical Chemistry)

1993

Mumbai University

II nd

Passed B.Sc with Chemistry as principal subject and Dyes & Drugs as applied component.I have done one year Post-graduate Diploma course in Industrial Analytical chemistry from Ramanarain Ruia college.

I have done M.Sc(By research) in Analytical Chemistry under the guidance of Prof.(Dr.)

R.T.Sane with thesis topic entitled”Devlopement of simple analytical methods in Drug Analysis.

Job responsibilities handled in the past jobs :

1)Sampling & analysis of raw materials (pharma formulations & bulk drugs) required for the manufacture of our products by Chemical & Instrumental methods of analysis.

2)Analysis of in-process and intermediate products by Chemical & Instrumental methods of of analysis.

3)Analysis of finished products(pharma formulations & bulk drugs) by Chemical & Instrumental methods of analysis.

4)Preparation of standard operating procedures(SOP’s) for operation & calibration of instruments.Preapration of STP

And for Pharma FP,RM,In-process.

Job responsibilities handling in the present job include :

1)Analysis of finished products by Chemical & Instrumental

Methods of analysis.

2)Analysis of intermediate & in process samples by Chemical & Instrumental methods of analysis.

3)Preparation of RM,FP specifications, SAP’s & formats as per the requirements & modifications.

4)Authorization & checking of analytical reports of Raw materials, vendor samples, finished products.

5)Development of simple, alternative analytical methods for new products & existing products.

6)Co-ordination with the stores and purchase department for the analysis of Raw Materials & Vendor samples approval.

7) Training & guidance to juniors when they come across any technical problem.

8)Handling the team of Juniors and guide them in day today work and co-ordinate With the External testing labs,RM vendors for RM Quality related problems, to face the External Audits.

9)To help the QA Dept is standardizing the Vendors for RM(Vendor Rating of Suppliers for RM)

10)To fill the customer questionnaire,prepare and send the CAPA of Audits

11)Issuance of BMR,Checking the BMR

12)To do the analysis of samples of Research Projects.& Industrial Projects samples on sophisticated analytical instruments.

13)To give the Hands on Training For Handling of sophisticated analytical instruments to the Research Students.

I am well versed with the handling of sophisticated analytical instruments like UV-Visible Spectrophotometer,FT-IR spectrophotometer,GC,HPLC,Auto-titrator & particle size analyzer.

Besides I have the knowledge about in-process quality control(IPQC) involved in pharmaceutical manufacturing processes like packaging, compression & labeling .Documentation I had prepared all the Specifications of RM,FP,and standard testing procedures of the same for WHO Audits,and familiar with documentation for ISO 9002.

Familiar with ERP & SAP system.

Analytical Instrumets Handled

i)UV-Visible spectrophotometer (Shimadzu UV-160A,UV-1700,UV-1800,Jasco V-530

UV-2600

ii)FT-IR Spectrophotometer(Shimadzu IR-430,Jasco FT-IR4100 Series,Shimadzu FT-IR 8400,Affinity-1

iii)Gas Chromatograph(GC) Chemito 8610,Shimadzu GC 2014 with Headspace,Perkin-Elmer Autosystem XL.

iv)HPLC Jasco 975 & 1525 HPLC model,Waters 1525 HPLC pump,2489UV-Vis detector,2707 autosampler with Millenium,Breeze 2 software,Waters Alliance 2695 with 2998 PDA detector and Empower 2 & Empower 3 software,Dionex Ultimate 3000 Quaternary HPLC system with Chromeleon Software.

Specific Target Achievement

Set up the instrument laboratory in Vedant Dyestuffs & intermediates with sophisticated analytical Instruments like HPLC,UV-Visible spectrophotometer along with their IQ/OQ/PQ in stipulated Time frame,and standardized the methods of 37 raw materials on HPLC including method devlopement for some RM,and started their Regular analysis simultaneously on HPLC in 12 months period.Was also involved in Standardization of Vendor’s of RM(Vendor Rating)

External Audits Faced

WHO Audits,MHRA Audit,Ethiopia,Uganda,Nigeria Regulatory Body Audits,Ukraine Regulatory Body Audit.

WORKING EXPERIENCE

I was working as “Trainee chemist” in SGS India Pvt Ltd for 6 months.(Period Oct 1991) to March 1992)

I was working as “Analytical chemist” in Sekhsaria Chemicals Pvt.Ltd for 22 months

(Period Oct 1992 to March 1994)

I was working as “Quality Control Officer” in Tata Pharma Ltd for about 42 months (Period Sept 1994 to March 1998)

I was working as “QC/QA Officer” in Hikal Ltd for about 45 months (Period July 1998 to March 2002)

I was working as “Senior Quality Control Executive” in Flamingo Pharmaceuticals Ltd for 50 months (Period April 2002 to May 2006)

I was working as “Senior Executive-Quality Control” in Ana zeal Analyticals & Research Pvt Ltd for 26 months (Period May 2006 to June 2008)

I was working as “Executive-Quality control in Inventia Healthcare Pvt Ltd at Ambernath (Period June 2008 to June 2010)

I Was working as “Assistant Manager QA/QC” in Vedant Dyestuffs & Intermediates at Taloja From June 2010 to Aug 2013)

I Was working as “QC/QA Incharge” in Jubilant Pharma & Chemical Lab” at Navi Mumbai From March 2014 to July 2014)

Was working as “Assistant Manager-Quality Control” in Neogen Chemicals Ltd

API Intermediate Mfg company(July 2014 to Nov 2016)

Was working as “Manager QC/QA in API Mfg company at Ambernath(August 2017 to

August 2018)

Was working as Lab Incharge –QC in Pharma Excepients Mfg company(Jan 2019 to May 2020)

At present working as “Technical Research Co-ordinator in Research based organization for last 18 months.

ADDITIONAL QUALIFICATIONS

I have got FDA approval in “Chemical & Instrumental analysis “section given by FDA Maharashtra state.

Drawn CTC : 4.80 lacs P.A

Expected CTC : As per the rules & regulations of the organization.

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