Resume /CV : QA / Regulatory Affairs

[amit020467]

Mr.Amit G.Dekate

To,
Respected sir/Madam

Sub :- submission of resume for regulatory affairs openings

Sir/madam,

Sending herewith my resume along with this as an attachment for openings along with you.
I am a post graduate in organic chemistry & having more than 4 yrs exp. In Pharma industry. I also completed my post graduate diploma in quality assurance & regulatory affairs.
Currently I works in API plant handling QA Documentation.

Kindly consider this application & revert back to me.

Thanking you
Amit g. Dekate

Curriculum Vitae :
amit24187730 AT hotmail.com

objective :
to be an essential part of an esteemed organization as well as an best performer
of the assigned work.

Personal information :
Nationality : Indian
Marital status : unmarried
Date of birth : 04/09/1981

Academic qualification :
M.SC. [organic chemistry] from mahrshi dayanand collage,
Parel, Mumbai University in oct-2004 with second class.
B.SC. [chemistry] from mahrshi dayanand collage
Parel, Mumbai University in march-2002 with second class.
H.SC. from Maharashtra state board in march-99 with second class
S.S.C. from Maharashtra state board in march –97 with first class

Project work :
_ the project is carried out during M.SC. Was
Conducts a seminar on the topic of ‘application of photochemistry’

Additional Qualification :
Completed Diploma in Quality Assurance from Institute of Pharma management, Dombivali.
Completed Diploma in Drug Regulatory Affairs from Institute of Pharma management, Dombivali.

personal traits :
Confident
Positive approach towards all situations
Interactive with people

Work experience :
1] Works with cipla ltd.
Q.C. chemist :During April-2005 to September- 2005
Job profile :
Physical as well as chemical analysis
Instruments handled like dissolution tester, UV-Visible spectrophotometer
Karl – fisher titrator. Etc.

2] Works with finornic chemicals pvt. Ltd.
research chemist :During April- 2006 to June –2006
Job profile :
Chemical process development for Mercaptons, API’S
Monitoring of chemical reaction through TLC fingerprinting, Literature search.

3] Works with charaka Pharma pvt. Ltd.
Q.C. Officer :since aug-2006 to May-2008
Job profile :
Analysis of stability products for their various active parameters
Chemical & instrumental analysis
Calibration & maintenance of instrument.
TLC fingerprinting.
Inst. Handled like spectrophotometer, viscometer, polar meter, refract meter.
Analysis of various generic products.

4] Works with Unique chemicals, mahape (A Div. of J.B.Chemicals & Pharmaceuticals Ltd. )
Q.A./Q.C Chemist :since May-2008 to October-2008
Job profile :
Working under SAP-LIMS system
Analysis of various Raw materials, Intermediate, Finish products, & packing materials.
Monitoring various in-process check-ups.
Issuing of BMR & other documents to the production dept.
Calibration & maintenance of various inst. In the lab.
Preparations & updating various Sops’ & STP’s of the lab.
Preparations of various validations protocols & reports.

5] works with Watson Pharma PVT.LTD.
Q.A. Officer :Since Oct-2008 to May-2009
Job profile :
Responsible for the quality of product & Maintaining GMP System of the plant.
Responsible for the approval of various intermediate, in-process materials, packing materials through System.
To carry out Self-inspection as per the CQA.
To maintained formal change control system
To review qualification documents
To handle Market complaints.
To prepare Annual Product Review.
To assist Regulatory for the various DMF submissions & updating them
To maintained the Trends for Compliance for various regulatory as well as customer audits
To review stability studies of the product

6] Currently works with Zydus Nycomed HealthcarePvt.Ltd.
Q.A. officer :since May-2009 to till date
job profile :
1. To prepare & review various standard operating procedures
2. To review various records for batch release & archiving
3. To Maintain & implement various QA system like Change Control , Deviation ,OOS , Market complaints
4. To handle technology transfer & regulatory related documents
5. To carry out stability studies of the product & review reports.
5. To carry out internal quality audits
6. To plan various activities for new API plant

Hobbies :
Reading, listening music.

Place : Mumbai
[Amit G. Dekate]

[arunadikonda]

CURRICULUM VITAE :
ARUNA N DIKONDA
Email id - arunadikonda AT rediffmail.com

Career Goal :
Fully utilize my technical and personal skills and grow with my organization, which could allow me to set new heights and standards in pharmacy industry by utilizing my present domain knowledge and responsible position in the organization that provide opportunities for growth, motivation to work.

EDUCATIONAL QUALIFICATION :
1) B. Pharmacy from Mumbai university with 64% in 2010.
2) D. Pharmacy from MSBTE with 80.20% in 2007.
3) HSC from Mumbai with 64.67% in 2005.
4) SSC from Mumbai with 59.33% in 2003.

PROJECTS PRESENTATION :
Project on :Antiobesity drugs done at Prin.K.M Kundnani College of Pharmacy
Report on : Antiobesity drugs.
Power point presentation of project.

Project on : Microencapsulation done at V.H.P.Shah College of Pharmacy
Report on :Microencapsulation its advances, preparation and its uses.
Power point presentation of project in College.

INDUSTRIAL VISIT AND EXCURSION :
Glaxosmithkline Pharmaceutical Company at Nashik

HOSPITAL VISIT :
Saifee Hospital at Churni Road

Experience details :
Work in Viresh Medical as Pharmacist
Experience : 6 months

Work in WELLNESS FOREVER MEDICAL Pvt. Ltd as Pharmacist
Experience : 6 months

Extra Curricular Activities :
Played active role in seminar presentation.

Computer Literacy :
Microsoft office – Word, Power point and Excel.
Typing speed - 23wpm

PERSONAL TRAITS :
* Dedicated and Punctual
* Pleasing personality
* Self motivated and ability to work in team
* Ability to communicate effectively orally and in writing
* Ability to prioritize workload
* Ability to exercise independent judgment, consistent with corporate and department guidelines

HOBBIES :
1) Reading books
2) Watching Movies
3) Listening to music

Areas of Interests :
* Regulatory affairs
* Quality Assurance
* Documentation
* Clinical Research