JYOTI YASHWANT PATIL

Address:

*** *,

* **** ****, ********.

Sector 16, Email Id: acds30@r.postjobfree.com.

New Panvel Mob. No.:090********

New Mumbai 410206

SUMMARY :-

Presently I am working in SGS Life science service India Pvt Ltd, Organization are engage with Testing (Pharmaceuticals & cosmetics Products), Inspection, certification, verification. Laboratory having NABL,FDA certification and cGMP Facility with well established Quality Control Laboratory .

OBJECTIVE:-

To build up a Analytical lab technician career, in which I utilize my technical & logical Skill.

EDUCATIONAL QUALIFICATION:-

Bachelor of science in chemistry with Applied Drug & Dyes. From Mumbai University In 2004.

COMPUTER SKILL:-

Diploma in computer Application In sterlight Foundation Institute, Basic knowledge of

Microsoft Word, Internet, Microsoft Excel, Microsoft Powder Point.

OTHER SKILL:-

Food drug Administration Approved in chemical & Instrument section in March 2012.

SUMMARY OF EXPERIENCE:-

• Working with SGS LSS India Pvt Ltd. As a Quality Control Executive

Work effective from. March. 2013 to till date.

• Working with Umang Pharmatech Pvt Ltd. As a Quality Control Executive.

Work effective from. Oct. 2008 to Feb 2013.

• Worked with Ideal Cures Private Ltd : As a Quality control Chemist

Period: Oct. 2005 to Sept 2008.

JOB PROFILE SGS LSS INDIA PVT LTD

Chemical & Instrumental Analysis of Pharmaceutical products and Consumer products of Finished product, Raw Material and Stability samples.

Responsible for method validation and method transfer.

Responsible for Instrument Calibration like HPLC, GC, FTIR, UV,KF etc.

Responsible for preparation and reviewing the Standard operating procedure in compliance with regulatory standard.

Co-ordinate in the regulatory/customer audit

Responsible for the authorization of test reports.

Review the Microbiology reports and documents.

Training given to new employee as per schedule.

Review of Micro Reports and records.

JOB PROFILE IN UMANG PHARMATECH PVT LTD

Chemical & Instrumental Analysis of Finished product, Raw Material, In process sample & Packing Material.

Carried out Dissolution test for SR,EC, IR, CR Pellets & granules like Aspirin EC & IR, Indomethacin SR, Caffeine IR, CR, Dichlofenac Na/ K SR, Domperidone SR, Orlistat IR, Bended product like Pracetamol 500mg, CPM 2mg, Phenylephirine HCL 10mg & Dextromethrphone Hydrobromide 15mg in 710mg pellets, Bromexine 8mg, salbutamol 4mg & Theophylline 200mg in 400mg pellets etc. on fully automated 8 stage dissolution apparatus on HPLC & UV.

Carry out Method Development under the guidance of Project in charge.

Upkeep of Analytical Equipments, Column Installation and preventive maintenance.

Preparation of Method, Report format as per standards.

Calibration of Instruments like GC, HPLC, UV, FTIR, Brookfield Viscometer Dissolution test Apparatus, Karl Fischer Titrator etc. technical problems and software

Stability Study of Finished Product as per the schedule.

Prepared working standard & maintained its uses records.

Prepared Sampling plain of Raw Material & Finished Product.

Raw material Analysis do for vender approval & keep its record

Maintain the reagent & chemical records

Given on job training to new chemist

Solve the queries of party related to quality control

Documentation Knowledge :

Maintain the validation documents like Process validation, Method validation, Personal Validation.

Maintain the instrument Calibration & Uses log book records.

Maintain the entry register of Raw Material, Finished Product, Packing Material its sampling report, GRN record

Prepared the Raw Material, Finished Product, Packing Material protocol & computerized report.

Prepared Material Safety Data Sheet.

Prepared BMR, BPR, MFR of Pharmaceutical pellets .

Prepared Specification of Raw Material, Finished Product, standard operating procedure & standard test Procedure.

Prepared & maintained Water analysis & regeneration record.

INSTRUMENT HANDLED:

a) High-performance Liquid Chromatography (Automatic Autosamler )

(Agilent Technology Model No.: Compact LC 1120 Software : Ezichrome Elight)

High-performance Liquid Chromatography (Automatic Autosamler )

( Shimadzu Model No.: LC 2010 CHT Software : LC 2000)

High-performance Liquid Chromatography (Mannual )

( Chemito Model No.: Software : Iris 32)

b) Gas Chromatography ( Perkins Elmer Software : Iris 32)

Gas Chromatography ( Chemito Software : Iris 32)

c) UV –VIS Double Beam Spectrophotometer

( Make : Chemito & Shimadzu Model No. UV 1700 )

d) Dissolution Test Apparatus (Labindia Model No.: Disso 2000

(Autosampler & Veego(Manual))

e) Fourier Transform Infrared Spectrophotometer (Shimadzu & Thermo)

f) Karl Fisher Titrator ( Labindia & Veego)

g) Viscometer (Brookfield )

h) Disintegration Tester (Electrolab Model No.: ED2L )

i) Premier Colour Scan Instrument ( Premier )

j) Fribilator (Eletrolab)

k) Refractometer (Dolphin & Rajdhjani )

l) Polarimeter (Rajdhani)

m) Particle Size Analyzer (Duro tap )

n) Hardness Tester (Expo Hitech)

o) IR Moisture Balance ( Rajdhani)

p) pH & Conductivity meter (Labindia & expo Hitech)

q) Bulk Density Appratus (Expo Hitech & Electolab)

r) Melting Point Appratus (Labindia & Veego)

s) Stability Chembers ( Thermolab)

t) Autoclave stem Sterilizers (Hally Equipments Meta lab)

u) Microscope (Dolphin & Rajdhani)

v) UV cabinet (Metalab)

w) USB scale (Sipcon)

Microbiology Knowledge :

Microbiological Limit test of Raw material, Finished Product, Packing Material ( TAMC, TYMC & Pathogen like Ecoli, Salmonella, Shigella, Pseudomonas, Staphylococcus auras.)

Swab analysis of equipment & Compressed Air Analysis.

Water Analysis by spread plate & Membrane filtration method

Growth Promotion study of Media

Sub culturing of master culture

Environmental Study ( By air sampling & By Plate Explosion )

Instrument calibration like Incubator, Refrigerator, DBK Colony counter etc.

Fumigation as per schedule.

Micro Documentation Knowledge:

Maintain the validation documents like Water validation, Cleaning validation, Compressed Air Validation.

Maintained Micro analysis reports & Records of analysis .

Maintained the entry Register & Instrument log book.

Maintained the Media records

Prepared Micro SOPs.

Worked with Ideal Cures Private Ltd :

Period: Oct. 2005 to Sept 2008.

JOB PROFILE

Chemical & Instrumental Analysis of finished product, Raw Material, Packing Material.

Calibration of Instrument like HPLC, UV, Dissolution test Apparatus, FTIR, KF etc.

Micro Biological Analysis & Micro Documentation.

Prepared & checking of Batch Manufacturing Records.

Prepared Specification as per IP & USP.

Prepared Standard test procedure

Stability Study of Finished Product.

Water Analysis & maintained its records.

Analyse sample for vendor approval & keep its records.

Training Attained :

• Attained 2 days GMP Training program conducted by Insight systems inc. Pune

07.08.2006 to 08.08.2006

• Also Attending one day training program on ISO 22000 by Akanshya Management Consultancy on 05.07.2010

• 15 days training program on Standard Operating Procedure of Customer complaint, OOS, CAPA, Deviation, Training orientation of new employee, GMP Training From 01 April 2013 to 15 April 2013 conducted by Ryan Glin QA Manager of SGS USA.

• One day training NABL by Shobhana Sharma SGS (Gurgoan) on 26.09.2013.

Audit Faced :

• Attend the WHO Audit in Ideal Cures Pvt Ltd Vasai Road (East), sept 2008. as a senior quality control chemist.

• Attend Party audit Colgate Palmolive Ltd (Maxico)in sept 2010 in Umang Pharmatech Pvt Ltd Vasai Road (East) as a senior quality executive.

• Attend Party audit Dr Reddy’s Hyderabad March 2012 in Umang Pharmatech Pvt Ltd Vasai Road (East) as a senior quality executive.

• Attend Party audit Lincolin Nov 2012 in Umang Pharmatech Pvt Ltd Vasai Road (East)

as a senior quality executive.

• Attend Jansen cilag on 16 June to 18 June 2013 in SGS LSS India Pvt Ltd in New Mumbai as a Quality Control Executive.

• Attend NABL (Preassessment) audit June 2013 in SGS LSS India Pvt Ltd in New Mumbai as a Quality Control Executive.

• Attend Cipla Audit 06 Aug 2013 in SGS LSS India Pvt Ltd in New Mumbai as a Quality Control Executive

• Attend NABL audit 17 oct 1013 & 18 Oct 2013. in SGS LSS India Pvt Ltd in New Mumbai as a Quality Control Executive

• Attend Jansen cilag on 30 Jan 2014 to 31 Jan 2014 in SGS LSS India Pvt Ltd in New Mumbai as a Quality Control Executive.

PERSONAL DETAILS:-

Date of Birth : 02.05.1984

Quality :Honest,Hard working & Puntual

Hobbies :Listening Music, Reading.

Marital status :Single

Nationality :Indian

Place : Jyoti Patil

Date:

JYOTI YASHWANT PATIL

Address:

104 E,

8 Kool Home, Contacts.

Sector 16, Email Id: acds30@r.postjobfree.com.

New Panvel Mob. No.:090********

New Mumbai 410206

SUMMARY :-

Presently I am working in SGS Life science service India Pvt Ltd, Organization are engage with Testing (Pharmaceuticals & cosmetics Products), Inspection, certification, verification. Laboratory having NABL,FDA certification and cGMP Facility with well established Quality Control Laboratory .

OBJECTIVE:-

To build up a Analytical lab technician career, in which I utilize my technical & logical Skill.

EDUCATIONAL QUALIFICATION:-

Bachelor of science in chemistry with Applied Drug & Dyes. From Mumbai University In 2004.

COMPUTER SKILL:-

Diploma in computer Application In sterlight Foundation Institute, Basic knowledge of

Microsoft Word, Internet, Microsoft Excel, Microsoft Powder Point.

OTHER SKILL:-

Food drug Administration Approved in chemical & Instrument section in March 2012.

SUMMARY OF EXPERIENCE:-

• Working with SGS LSS India Pvt Ltd. As a Quality Control Executive

Work effective from. March. 2013 to till date.

• Working with Umang Pharmatech Pvt Ltd. As a Quality Control Executive.

Work effective from. Oct. 2008 to Feb 2013.

• Worked with Ideal Cures Private Ltd : As a Quality control Chemist

Period: Oct. 2005 to Sept 2008.

JOB PROFILE SGS LSS INDIA PVT LTD

Chemical & Instrumental Analysis of Pharmaceutical products and Consumer products of Finished product, Raw Material and Stability samples.

Responsible for method validation and method transfer.

Responsible for Instrument Calibration like HPLC, GC, FTIR, UV,KF etc.

Responsible for preparation and reviewing the Standard operating procedure in compliance with regulatory standard.

Co-ordinate in the regulatory/customer audit

Responsible for the authorization of test reports.

Review the Microbiology reports and documents.

Training given to new employee as per schedule.

Review of Micro Reports and records.

JOB PROFILE IN UMANG PHARMATECH PVT LTD

Chemical & Instrumental Analysis of Finished product, Raw Material, In process sample & Packing Material.

Carried out Dissolution test for SR,EC, IR, CR Pellets & granules like Aspirin EC & IR, Indomethacin SR, Caffeine IR, CR, Dichlofenac Na/ K SR, Domperidone SR, Orlistat IR, Bended product like Pracetamol 500mg, CPM 2mg, Phenylephirine HCL 10mg & Dextromethrphone Hydrobromide 15mg in 710mg pellets, Bromexine 8mg, salbutamol 4mg & Theophylline 200mg in 400mg pellets etc. on fully automated 8 stage dissolution apparatus on HPLC & UV.

Carry out Method Development under the guidance of Project in charge.

Upkeep of Analytical Equipments, Column Installation and preventive maintenance.

Preparation of Method, Report format as per standards.

Calibration of Instruments like GC, HPLC, UV, FTIR, Brookfield Viscometer Dissolution test Apparatus, Karl Fischer Titrator etc. technical problems and software

Stability Study of Finished Product as per the schedule.

Prepared working standard & maintained its uses records.

Prepared Sampling plain of Raw Material & Finished Product.

Raw material Analysis do for vender approval & keep its record

Maintain the reagent & chemical records

Given on job training to new chemist

Solve the queries of party related to quality control

Documentation Knowledge :

Maintain the validation documents like Process validation, Method validation, Personal Validation.

Maintain the instrument Calibration & Uses log book records.

Maintain the entry register of Raw Material, Finished Product, Packing Material its sampling report, GRN record

Prepared the Raw Material, Finished Product, Packing Material protocol & computerized report.

Prepared Material Safety Data Sheet.

Prepared BMR, BPR, MFR of Pharmaceutical pellets .

Prepared Specification of Raw Material, Finished Product, standard operating procedure & standard test Procedure.

Prepared & maintained Water analysis & regeneration record.

INSTRUMENT HANDLED:

a) High-performance Liquid Chromatography (Automatic Autosamler )

(Agilent Technology Model No.: Compact LC 1120 Software : Ezichrome Elight)

High-performance Liquid Chromatography (Automatic Autosamler )

( Shimadzu Model No.: LC 2010 CHT Software : LC 2000)

High-performance Liquid Chromatography (Mannual )

( Chemito Model No.: Software : Iris 32)

b) Gas Chromatography ( Perkins Elmer Software : Iris 32)

Gas Chromatography ( Chemito Software : Iris 32)

c) UV –VIS Double Beam Spectrophotometer

( Make : Chemito & Shimadzu Model No. UV 1700 )

d) Dissolution Test Apparatus (Labindia Model No.: Disso 2000

(Autosampler & Veego(Manual))

e) Fourier Transform Infrared Spectrophotometer (Shimadzu & Thermo)

f) Karl Fisher Titrator ( Labindia & Veego)

g) Viscometer (Brookfield )

h) Disintegration Tester (Electrolab Model No.: ED2L )

i) Premier Colour Scan Instrument ( Premier )

j) Fribilator (Eletrolab)

k) Refractometer (Dolphin & Rajdhjani )

l) Polarimeter (Rajdhani)

m) Particle Size Analyzer (Duro tap )

n) Hardness Tester (Expo Hitech)

o) IR Moisture Balance ( Rajdhani)

p) pH & Conductivity meter (Labindia & expo Hitech)

q) Bulk Density Appratus (Expo Hitech & Electolab)

r) Melting Point Appratus (Labindia & Veego)

s) Stability Chembers ( Thermolab)

t) Autoclave stem Sterilizers (Hally Equipments Meta lab)

u) Microscope (Dolphin & Rajdhani)

v) UV cabinet (Metalab)

w) USB scale (Sipcon)

Microbiology Knowledge :

Microbiological Limit test of Raw material, Finished Product, Packing Material ( TAMC, TYMC & Pathogen like Ecoli, Salmonella, Shigella, Pseudomonas, Staphylococcus auras.)

Swab analysis of equipment & Compressed Air Analysis.

Water Analysis by spread plate & Membrane filtration method

Growth Promotion study of Media

Sub culturing of master culture

Environmental Study ( By air sampling & By Plate Explosion )

Instrument calibration like Incubator, Refrigerator, DBK Colony counter etc.

Fumigation as per schedule.

Micro Documentation Knowledge:

Maintain the validation documents like Water validation, Cleaning validation, Compressed Air Validation.

Maintained Micro analysis reports & Records of analysis .

Maintained the entry Register & Instrument log book.

Maintained the Media records

Prepared Micro SOPs.

Worked with Ideal Cures Private Ltd :

Period: Oct. 2005 to Sept 2008.

JOB PROFILE

Chemical & Instrumental Analysis of finished product, Raw Material, Packing Material.

Calibration of Instrument like HPLC, UV, Dissolution test Apparatus, FTIR, KF etc.

Micro Biological Analysis & Micro Documentation.

Prepared & checking of Batch Manufacturing Records.

Prepared Specification as per IP & USP.

Prepared Standard test procedure

Stability Study of Finished Product.

Water Analysis & maintained its records.

Analyse sample for vendor approval & keep its records.

Training Attained :

• Attained 2 days GMP Training program conducted by Insight systems inc. Pune

07.08.2006 to 08.08.2006

• Also Attending one day training program on ISO 22000 by Akanshya Management Consultancy on 05.07.2010

• 15 days training program on Standard Operating Procedure of Customer complaint, OOS, CAPA, Deviation, Training orientation of new employee, GMP Training From 01 April 2013 to 15 April 2013 conducted by Ryan Glin QA Manager of SGS USA.

• One day training NABL by Shobhana Sharma SGS (Gurgoan) on 26.09.2013.

Audit Faced :

• Attend the WHO Audit in Ideal Cures Pvt Ltd Vasai Road (East), sept 2008. as a senior quality control chemist.

• Attend Party audit Colgate Palmolive Ltd (Maxico)in sept 2010 in Umang Pharmatech Pvt Ltd Vasai Road (East) as a senior quality executive.

• Attend Party audit Dr Reddy’s Hyderabad March 2012 in Umang Pharmatech Pvt Ltd Vasai Road (East) as a senior quality executive.

• Attend Party audit Lincolin Nov 2012 in Umang Pharmatech Pvt Ltd Vasai Road (East)

as a senior quality executive.

• Attend Jansen cilag on 16 June to 18 June 2013 in SGS LSS India Pvt Ltd in New Mumbai as a Quality Control Executive.

• Attend NABL (Preassessment) audit June 2013 in SGS LSS India Pvt Ltd in New Mumbai as a Quality Control Executive.

• Attend Cipla Audit 06 Aug 2013 in SGS LSS India Pvt Ltd in New Mumbai as a Quality Control Executive

• Attend NABL audit 17 oct 1013 & 18 Oct 2013. in SGS LSS India Pvt Ltd in New Mumbai as a Quality Control Executive

• Attend Jansen cilag on 30 Jan 2014 to 31 Jan 2014 in SGS LSS India Pvt Ltd in New Mumbai as a Quality Control Executive.

PERSONAL DETAILS:-

Date of Birth : 02.05.1984

Quality :Honest,Hard working & Puntual

Hobbies :Listening Music, Reading.

Marital status :Single

Nationality :Indian

Place : Jyoti Patil

Date:

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