OFFICIAL LETTER

From

T. Ashok M Pharm.,
39 A Gandhi Road,
Uthangarai (Po)
Pincode-635207
Krishnagiri (D.T)

To

The H R Department,

Respected Sir,

Sub: Applying for the post of Executive-QA in your esteemed Organization-Reg

I wish to inform you that I have successfully completed M.Pharm (Pharmaceutics) in J.S.S
College of Pharmacy, Ooty during the year 2009-2011.At present I am working as an Officer-QA
in Caplin Point Ltd, Chennai Since 17th March-2016. I ensure you to understand that there are
some vacancies in your esteemed organization. I present myself as a candidature for the Said post
and I have enclosed my resume for your kind perusal.

Hence I request you to kindly pursue my application and offer me an opportunity to work, I
assure that I will discharge my duties to the entire satisfaction of my Superiors and abide the rules
& regulations of the Organization.

I request you to favorable order please

Thanking you with anticipation

Place: Yours Sincerely,

Date: (Ashok.T)
 CURRICULUM-VITAE OBJECTIVE

T.ASHOK M.Pharm., To seek a challenging and rewarding position with

E-mail ID: tashok1985@gmail.com opportunity to continue, to advance and to develop my skills with a
tashok1985@yahoo.com
progressive and nurturing organization.To make significant
Permanent Address contribution in the field of drug research, develop, good human
39-A Gandhi Road, relation and thus to be instrumental in the organizations growth.
Uthangarai (PO)
Krishnagiri (Dist)
Pin code-635207 PROFESSIONAL QUALIFICATION
Tamilnadu

Name of the Year of Percentage

Mobile No.: +91 9894398334 S.No Qualification
institution Passing Obtained
Personal Data
1. M.Pharm J.S.S College of 2009-2011 73%
Father’s Name:
(Pharmaceutics) pharmacy, Ooty
T.S.Thirunathan
2. Bachelor of Annamalai 2004-2008 62%
Date of Birth : 09.01.1986 pharmacy University,
Chidambaram
Marital Status : Married

Nationality : Indian
PROJECT WORK
Sex : Male
M. Pharm:
Hobbies & Interests  Dissolution enhancement of poorly water soluble drug
- Reading Books using Glibenclamide by Liquisolid Compact Technique.
- Referring Journals
- Making Friends B.Pharm:
- Listening Music  Prescriber Software Using Visual Basic 6.0
- Research

Languages Known COMPUTER SKILLS

-English
 M.S.Office
-Tamil  Basic and Internet skills
PROFESSIONAL EXPERIENCE

 Presently working as an Officer-QA in Caplin point Laboratories Ltd, Chennai for

manufacturer of Injectables approved by USFDA, European Markets, ANVISA
(Brazil) from March 2016 to till Date.

 Worked as an “Executive-Production” in Geltec-Innovative Healthcare Private

Ltd, Bangalore for the manufacturing of oral dosage forms approved by TGA
(Tablets, Capsule Section) from July-2nd 2014 to Feb-2016.

 Worked as an “Executive-Production” in Saimirra Innopharm Private Ltd,

Chennai for the manufacturing of oral dosage forms approved by WHO-GMP
(Tablets, Capsules, and Liquid Section) from September-5th 2013 to June-2014.

 Worked as an “Executive-Production” in Micro labs Ltd, Hosur for the

manufacturing of oral dosage forms (tablets section) from July-7th2011-August-
31-2013

JOB DESCRIPTION AND RESPONSIBILITIES

 Responsible for Issuance of Training Questionnaires to concerned Departments by

using QA Issued with sign and Date
 Responsible for Issuance and Retrieval of Logbooks to concerned Departments
according to Document control system SOP
 Responsible for Monitoring the controlled Samples
 Review of SOPs, Analytical work sheet, STP, SPCs, Finished Product, Stability etc…
 Responsible for maintaining the balance usage log sheet and forth night Calibration log
book.
 Issuance and Retrieval of SOPs, AWS, STP,SPCs, Finished product, Stability and
recorded in document controlled sheet
 Responsible for maintaining the daily record for Temperature, Relative Humidity, and
Differential pressure record.
 Responsible for conducting Training Matrix, Refresher Training, Initial Training,
CGMP with respect to Annual Training Schedule
 Maintaining the Documents with Respect to Data Integrity
 Handling of Quality Management Systems
 Good Documentation Practices
 Document control System
 Self Inspection
 Responsible of Maintaining Document Archival and Retrieval System
 Responsible for Maintaining Sop Master Index during SOP Revision
 Responsible for Maintaining the Master list of Equipments, and Components
 Preparation of Issuance, Control, Retrieval, and Destruction of batch Records
 Responsible for Monitoring of TOC Analyzer in QC Department
 Responsible for Review of Sops
 Review of Analytical Documents and Log Books

STRENGTHS

 Ability to work hard as team player as well as individual with excellent

communication Skills.

 Ability to work in rapidly changing environment.

 To utilize my skills and abilities for the development of the company and
thereby achieve a challenging and responsible position.
 Good Convincing Capability
 Punctual and self-Discipline
 High Confidence and Decision Making
AUDITS FACED

 USFDA (US)
 UNICEF
 WHO (Geneva)
 TGA (Australia)
 IDA (Netherland)
 EUGMP

WORK EXPERIMENTS WITH HANDLING MACHINES

 Handling of Production Equipment’s like RMG, FBD, Sifter, Multi-Mill in Granulation

 Tablet Compression Machine
 TOC Analyzer
 Viscometer
 Conductivity meter
 ph. Meter
 Handling of analytical instruments like UV-Spectrophotometer, and Dissolution
apparatus etc.

DECLARATION

I hereby declare that the statements furnished are true and complete to the best of my
knowledge and belief.

Thanking you

Place: Yours sincerely,

Date: (ASHOK.T)