APPLICATION
Gadara Kalpesh Amarshibhai
Flat No. 301, Tower - D
Lakshya Avenue, Nr. Vaikunth-2,
Khodiyarnagar cross road,
New Karelibaug, Baroda
State : Gujarat
Phone No.(+91)8905239390/
9909515169
Date:
To,
______________________
______________________
______________________
______________________
Subject: - An Application for the post of Suitable Position in Pharmaceutical Formulation.
Dear Sir,
I would like to apply for the post of suitable position in Pharmaceutical Formulation. I would
like to enroll my name as one of the competent candidate for that post.
I enthusiastically looking out for a better Prospective and challenging career in the
Pharmaceutical industry through your esteemed organization. Hence,I request you to consider
myself as a prospective candidate to work in your firm.
I assure you that if I am selected for the job. I will make you satisfy by my desired subject
knowledge and hard work. My C.V. and other details are enclosed here.
Looking forward to contribute for the success of your organization.
PROFESSIONAL QUALIFICATION:”B.PHARMA”
Hoping for positive response from your end.
Thanking you
Yours Sincerely
(Gadara Kalpesh A.)
KALPESH A. GADARA
Address for Correspondence Permanent Address
Flat No. 301, Tower – D, A/p : Khengarka.
Lakshya Avenue, Nr. Vaikunth-2, Taluka: Dhrol
Khodiyarnagar cross road, Dist : Jamnagar - 361210
New Karelibaug, Baroda. State : Gujarat
State: Gujarat .
Phone No. (+91)8905239390 Phone No :( +91)9909515196
Excellent organizational skills, an ability to work hard and learn quickly together with a strong
academic background & exposure of individual handling of Production activities. Now I wish to use
my skills and undertake further training with a view to moving into Pharmaceutical Industry.
Around 8 years of experience in the field of Production in Pharmaceutical formulation and Duly
approved in Liquid Oral Section on form no. 25 & 28 (Allopathic System Of Medicine) by FDA
Uttarakhand in 02-03-2009.
I have also got duly approved in External Preparation section (Metered Dose Inhaler, Nasal
Spray, Dry Powder Inhaler and Cream / Gel) from Sun Pharmaceutical Industries Ltd, Halol
by FDA, Gujarat in 2013.
Exposure in following dosage form.
Aerosol : Nasal Spray, Metered Dose Inhaler (MDI) and Dry Powder Inhaler (DPI)
Liquid Oral: All types of syrup, Suspension, drops.
External preparation (Semisolid Dosage) : Gel, Cream
CURRICULUM VITAE
Overview
Career Objective
• Name ………………………… Kalpesh A. Gadara
• Date of Birth ……………….. 23th
July 1984
• Father Name ………………… Mr. Amarshibhai N. Gadara
• Marital Status……………….. Married.
• Nationality. ………………… Indian
• Religion …………………….. Hindu
• Sex ………………………… Male
• Languages Known ………….. Gujarati, Hindi and English
• E-mail………………………... kalpesh.gadara@gmail.com,
kalpesh_gadara@yahoo.co.in
HOBBIES & INTERESTS
I have keen interest in studying all kinds of societies all over the world, knowing people and
traveling. Watching Comedy programme and cricket in free time.
• Presently associated with Sun Pharmaceutical Industries Ltd. (USFDA,MHRA,
TGA, INVISA,ICH Approved Plant),Halol(Gujarat) since 19th
Feb- 2010 to till date as
a SENIOR EXECUTIVE in Aerosol (Metered Dose Inhaler, Nasal spray, Dry
powder inhaler (DPI) and External Preparation Department.
 Approved as Technical Person by FDA Gujarat in External Preparation
Section
• Had worked with Coral Laboratories Ltd, WHO, ISO 9001-2000 certified
organization from 16th
November 2009 to 13th
Feb-2010 as a Production
Executive in liquid oral and external preparation area.
• Had worked with Hema Laboratories Pvt. Ltd. As a Junior Production
Executive in a Liquid Oral, Tablet and Dry Syrup (Cephalosporin) Section
from 1st
Sept-2008 to 13th
Nov-2009.
 Approved as Technical Person by FDA Uttarakhand
(N: 17P/8/90/2001/7979, Dated 02-03-2009) in Liquid Oral Manufacturing.
Professional Experience
PERSONAL PROFILE
• Had worked as a Technical Supervisor in a SOFT GELATIN CAPSULE Department
in Casil Industries Ltd (A Member Group Of Cadila Pharmaceutical Ltd.) from
6th
May2007 to 27th
Aug 2008.
In Sun Pharmaceutical Industries Ltd :
• To assist the Manager in batch manufacturing and packing of department.
• Responsible for the day to day production planning.
• As per daily production planning, to generate work order for raw material through ERP
system then send work order to warehouse for dispensing of raw material.
• To co-ordinate with warehouse for issuance of raw materials to achieve schedule plan.
• Work allocation to the supervisors & operators as per daily production planning.
• Responsible for controlling a system in accordance with all cGMP regulatory
guidelines.
• Monitor and control the operator for standardize production activity to achieve better
productivity and quality.
• To provide training to supervisors & operators as per SOP and cGMP whenever
required.
• To conduct & provide on job training to supervisors and operators as per yearly
departmental training calendar.
• To prepare daily report of menpower utilization and production output and discussion to
be done with department head.
• To prepare WIP, Monthly and Quarterly Report as when required.
• To Prepare, updation, approval of MBMR/MBPR/SOP whenever required.
• To prepare qualification protocol of new equipment then do Qualification (IQ,OQ,PQ)
of same in presence of Quality Engineering person.
• To perform the investigation report against any failure in batches and take corrective
action against failure, close the CAPA as when required.
Documentation:
• Maintain all GMP documents like sequential log of equipment, daily balance
performance record, temp–humidity record, room differential pressure record.
Job Responsibilities
• Maintain all housekeeping records like cleaning and sanitation solution preparation
record, Daily cleaning and sanitation record, Weekly/Monthly cleaning record, weekly
drain sanitation record.
• Have worked on cost reduction processes.
• Enforcement of manpower for better productivity, prepared records of productivity.
• Improvement of product quality with quantity day by day.
• Faced regulatory audits of WHO, USFDA, MHRA, TGA, INVISA.
● Preparation of Process validation protocol of new ANDA products.
• Supervised along with F&D department for development of new products in the form of
Metered Dose Inhaler (MDI), Nasal spray and Dry powder inhaler (DPI) dosage form.
• Knowledge of some QA concept like Plan modification Form (PMF), Change control,
Incident, CAR, FMEA, Effectiveness Check.
• Faced as a auditee internal quality audit as per schedule conducted by quality assurance
department as per schedule and compliance of IQA audit observation.
SR
NO.
DEGREE NAME OF
COLLEGE
NAME OF UNIVERSITY YEAR OF
PASSING
PERCENTAGE
OF MARKS
RESULT
1 B. Pharma The oxford
college of
pharmacy
R.G.U.H.S. 2006 71% Distinction
2 H.S.C K.C.Kothari
Higher
Secondary
School
G.S.E.B.Gandhinaga
r
March-
2002
58.00% Second
Class
3 S.S.C K.C.Kothari
Higher
Secondary
School
G.S.E.B.Gandhinaga
r
March-
2000
71.00% Distinction
Professional Skill
Professional Qualification
Computer Knowledge: Windows, MS-Office, Internet.
• Production of pharmaceutical formulations
● Manufacturing Science & Technology (MSTG)
• Production Planning and Inventory Control (PPIC)
• Available on demand.
I, hereby declare that the particulars given above are true to the best of my
knowledge.
Date: Signature :
Place:
Professional Areas of interest
Declaration
Reference
Computer Knowledge: Windows, MS-Office, Internet.
• Production of pharmaceutical formulations
● Manufacturing Science & Technology (MSTG)
• Production Planning and Inventory Control (PPIC)
• Available on demand.
I, hereby declare that the particulars given above are true to the best of my
knowledge.
Date: Signature :
Place:
Professional Areas of interest
Declaration
Reference

Latest CV

  • 1.
    APPLICATION Gadara Kalpesh Amarshibhai FlatNo. 301, Tower - D Lakshya Avenue, Nr. Vaikunth-2, Khodiyarnagar cross road, New Karelibaug, Baroda State : Gujarat Phone No.(+91)8905239390/ 9909515169 Date: To, ______________________ ______________________ ______________________ ______________________ Subject: - An Application for the post of Suitable Position in Pharmaceutical Formulation. Dear Sir, I would like to apply for the post of suitable position in Pharmaceutical Formulation. I would like to enroll my name as one of the competent candidate for that post. I enthusiastically looking out for a better Prospective and challenging career in the Pharmaceutical industry through your esteemed organization. Hence,I request you to consider myself as a prospective candidate to work in your firm. I assure you that if I am selected for the job. I will make you satisfy by my desired subject knowledge and hard work. My C.V. and other details are enclosed here. Looking forward to contribute for the success of your organization. PROFESSIONAL QUALIFICATION:”B.PHARMA” Hoping for positive response from your end. Thanking you Yours Sincerely (Gadara Kalpesh A.)
  • 2.
    KALPESH A. GADARA Addressfor Correspondence Permanent Address Flat No. 301, Tower – D, A/p : Khengarka. Lakshya Avenue, Nr. Vaikunth-2, Taluka: Dhrol Khodiyarnagar cross road, Dist : Jamnagar - 361210 New Karelibaug, Baroda. State : Gujarat State: Gujarat . Phone No. (+91)8905239390 Phone No :( +91)9909515196 Excellent organizational skills, an ability to work hard and learn quickly together with a strong academic background & exposure of individual handling of Production activities. Now I wish to use my skills and undertake further training with a view to moving into Pharmaceutical Industry. Around 8 years of experience in the field of Production in Pharmaceutical formulation and Duly approved in Liquid Oral Section on form no. 25 & 28 (Allopathic System Of Medicine) by FDA Uttarakhand in 02-03-2009. I have also got duly approved in External Preparation section (Metered Dose Inhaler, Nasal Spray, Dry Powder Inhaler and Cream / Gel) from Sun Pharmaceutical Industries Ltd, Halol by FDA, Gujarat in 2013. Exposure in following dosage form. Aerosol : Nasal Spray, Metered Dose Inhaler (MDI) and Dry Powder Inhaler (DPI) Liquid Oral: All types of syrup, Suspension, drops. External preparation (Semisolid Dosage) : Gel, Cream CURRICULUM VITAE Overview Career Objective
  • 3.
    • Name …………………………Kalpesh A. Gadara • Date of Birth ……………….. 23th July 1984 • Father Name ………………… Mr. Amarshibhai N. Gadara • Marital Status……………….. Married. • Nationality. ………………… Indian • Religion …………………….. Hindu • Sex ………………………… Male • Languages Known ………….. Gujarati, Hindi and English • E-mail………………………... kalpesh.gadara@gmail.com, kalpesh_gadara@yahoo.co.in HOBBIES & INTERESTS I have keen interest in studying all kinds of societies all over the world, knowing people and traveling. Watching Comedy programme and cricket in free time. • Presently associated with Sun Pharmaceutical Industries Ltd. (USFDA,MHRA, TGA, INVISA,ICH Approved Plant),Halol(Gujarat) since 19th Feb- 2010 to till date as a SENIOR EXECUTIVE in Aerosol (Metered Dose Inhaler, Nasal spray, Dry powder inhaler (DPI) and External Preparation Department.  Approved as Technical Person by FDA Gujarat in External Preparation Section • Had worked with Coral Laboratories Ltd, WHO, ISO 9001-2000 certified organization from 16th November 2009 to 13th Feb-2010 as a Production Executive in liquid oral and external preparation area. • Had worked with Hema Laboratories Pvt. Ltd. As a Junior Production Executive in a Liquid Oral, Tablet and Dry Syrup (Cephalosporin) Section from 1st Sept-2008 to 13th Nov-2009.  Approved as Technical Person by FDA Uttarakhand (N: 17P/8/90/2001/7979, Dated 02-03-2009) in Liquid Oral Manufacturing. Professional Experience PERSONAL PROFILE
  • 4.
    • Had workedas a Technical Supervisor in a SOFT GELATIN CAPSULE Department in Casil Industries Ltd (A Member Group Of Cadila Pharmaceutical Ltd.) from 6th May2007 to 27th Aug 2008. In Sun Pharmaceutical Industries Ltd : • To assist the Manager in batch manufacturing and packing of department. • Responsible for the day to day production planning. • As per daily production planning, to generate work order for raw material through ERP system then send work order to warehouse for dispensing of raw material. • To co-ordinate with warehouse for issuance of raw materials to achieve schedule plan. • Work allocation to the supervisors & operators as per daily production planning. • Responsible for controlling a system in accordance with all cGMP regulatory guidelines. • Monitor and control the operator for standardize production activity to achieve better productivity and quality. • To provide training to supervisors & operators as per SOP and cGMP whenever required. • To conduct & provide on job training to supervisors and operators as per yearly departmental training calendar. • To prepare daily report of menpower utilization and production output and discussion to be done with department head. • To prepare WIP, Monthly and Quarterly Report as when required. • To Prepare, updation, approval of MBMR/MBPR/SOP whenever required. • To prepare qualification protocol of new equipment then do Qualification (IQ,OQ,PQ) of same in presence of Quality Engineering person. • To perform the investigation report against any failure in batches and take corrective action against failure, close the CAPA as when required. Documentation: • Maintain all GMP documents like sequential log of equipment, daily balance performance record, temp–humidity record, room differential pressure record. Job Responsibilities
  • 5.
    • Maintain allhousekeeping records like cleaning and sanitation solution preparation record, Daily cleaning and sanitation record, Weekly/Monthly cleaning record, weekly drain sanitation record. • Have worked on cost reduction processes. • Enforcement of manpower for better productivity, prepared records of productivity. • Improvement of product quality with quantity day by day. • Faced regulatory audits of WHO, USFDA, MHRA, TGA, INVISA. ● Preparation of Process validation protocol of new ANDA products. • Supervised along with F&D department for development of new products in the form of Metered Dose Inhaler (MDI), Nasal spray and Dry powder inhaler (DPI) dosage form. • Knowledge of some QA concept like Plan modification Form (PMF), Change control, Incident, CAR, FMEA, Effectiveness Check. • Faced as a auditee internal quality audit as per schedule conducted by quality assurance department as per schedule and compliance of IQA audit observation. SR NO. DEGREE NAME OF COLLEGE NAME OF UNIVERSITY YEAR OF PASSING PERCENTAGE OF MARKS RESULT 1 B. Pharma The oxford college of pharmacy R.G.U.H.S. 2006 71% Distinction 2 H.S.C K.C.Kothari Higher Secondary School G.S.E.B.Gandhinaga r March- 2002 58.00% Second Class 3 S.S.C K.C.Kothari Higher Secondary School G.S.E.B.Gandhinaga r March- 2000 71.00% Distinction Professional Skill Professional Qualification
  • 6.
    Computer Knowledge: Windows,MS-Office, Internet. • Production of pharmaceutical formulations ● Manufacturing Science & Technology (MSTG) • Production Planning and Inventory Control (PPIC) • Available on demand. I, hereby declare that the particulars given above are true to the best of my knowledge. Date: Signature : Place: Professional Areas of interest Declaration Reference
  • 7.
    Computer Knowledge: Windows,MS-Office, Internet. • Production of pharmaceutical formulations ● Manufacturing Science & Technology (MSTG) • Production Planning and Inventory Control (PPIC) • Available on demand. I, hereby declare that the particulars given above are true to the best of my knowledge. Date: Signature : Place: Professional Areas of interest Declaration Reference