CURRICULUM VITAE:
Mr. Haresh Baban Nirmal
Vista Luxuria, Pune-Solapur Road,
Hadapsar, Tal : Haveli, Dist.: Pune-412307
Mob : +91-9096565886 / +91-7030683204
Email ID : nirmalharesh308 AT yahoo.com, nirmalharesh308 AT gmail.com
Objective :
To work in an organization where innovation and excellence is way of life where my full potential will be fully explored for the advancement and benefit of that company.
Professional Experience :
Total Experience : More than 3.6 Years in Sterile, MDI, Cosmeceuticals, Medical Devices
Action Medical Pvt. Ltd., Pune (ISO 9001 :2008 & ISO 13485:2003 Certified)
Executive-QA, March 2016 – Current
Duties :
** To carry out routine inspection of all departments for GMP Compliances
** Handling of CAPA
** Controlling all the documents related to QA
** Participation in line clearance & IPQA activity in production areas
** Assist in production planning and execution of batches
Midas- Care Pharmaceuticals Ltd., Waluj(WHO-GMP, MHRA approved)
Officer-QA, November 2014 – Jul 2015
Duties :
** Handling of Change control
** Preparation and review of Annual Product Reports & MFR
** Handled of IPQA activities in MDI, External sprays.
Aditi Pharmaceuticals Pvt. Ltd., Solapur(WHO-GMP approved)
Chemist-QA, December 2012 to November 2014
Duties :
** Preparation of BMR/BPR
** Review of Batch Manufacturing Record (BMR) and Batch Packaging Record (BPR)
** Preparation, Review , distribution and retrieval of SOP
** Preparation and review of process validation protocols and reports
** Handling of Deviations , Market complaints
** Handled of IPQA activities in Liquid Injectables, FFS, Dry powder, External Spray
CIPLA Ltd., (C/o : Aditi Pharmaceuticals Pvt. Ltd., Solapur)
LL Representative,February 2012 to October 2012
Duties :
** Weekly and monthly planning and execution of production batches
** To ensure availability of technical documents at LL site
** Review of Batch Manufacturing Record (BMR) and Batch Packaging Record (BPR)
** To investigate market complaint/Depot inspection to resolve critical issues
** To implement calibration and validation activities at LL site
** To Prepare DPR & monthly reports
** Monthly physical stock checking at concerned LL location
** Routine co-ordination with PPIC, CQA, RA etc.
Validation Knowledge:
** Area Validation, Bung processor and Tunnel validation, Media Fill Validation
** Washing, Filling & sealing machine validation and leak test machine validation
Audit faced :
FDA Maharashtra Audit, WHO-GMP Regulatory Audit, NAFDAC, CIPLA Ltd.,
DRL, Ranbaxy Laboratories Ltd.,
Industrial Training & Certification :
One monthtraining in Store, Production (Tablet and Capsule), Q.C.
Dept. at Maxheal Pharmaceutical, Satpur, Nashik.
Educational Details :
** M.Pharm.QA (October, 2010) from P.S.G.V.P.M’s College of Pharmacy, Shahada, North Maharashtra University with 64.00%
** B.Pharm ( July, 2008) from M.G.V.’s Pharmacy College, Nashik , Pune University with 60.50%
** D.Pharm ( June, 2005) from P.R.C.O.P , Loni, MSBTE with 82.30%
** H.S.C. (June, 2003) from P.V.P. College,Pune Divisional Board with 74.67%
** S.S.C ( June, 2001) from P.Dr.V.V.Patil Vidyalaya,Loni,Pune Board with 80.66%
Skills :
Instrument Handling Skills :
UV-VIS Spectrophotometer (Shimadzu/ Systronics), Colourimeter, Conductometer, Flourimeter, Digital Polarimeter, Dissolution Test apparatus)
Language known : English, Hindi & Marathi.
Computer Skill : Microsoft Office, Microsoft Word, Microsoft Power point, Internet surfing
Extra-curricular activity :
** Participated in M.C.C at School level
** Participated as Volleyball team representative at College level.
Declaration :
I hereby declared that the above mentioned information is correct to best of my knowledge.
Date : / /2016
Place : (Mr. H.B.Nirmal)