Ashok Vadithya is applying for a suitable position in quality assurance. He has 4 years of experience in quality assurance at Dr. Reddy's Laboratories and Mylan Laboratories. He holds an M.Pharm in Pharmaceutics from Osmania University and has experience with regulatory audits and ensuring compliance with cGMP. He is looking to contribute his skills and experience to quality assurance at a growing pharmaceutical organization.

1. .
APPLICATION
Ashok.Vadithya
Telephone: (M) 09666387130, 09491328733
E-mail: ashok.vadithya@gmail.com
Subject: - Application for suitable post in Quality Assurance in your esteemed
organization.
Experience: - Four Years’ experience in Non-sterile (Tablets, Capsule) Manufacturing
plant.
Current designation: - Asst.Manager-Quality Assurance.
Organization: - Dr.Reddy’s Loboratories Ltd (Hyderabad, Bollaram).
Educational Qualification: - M.Pharm (Master of pharmacy) in
Pharmaceutics.
RespectedSir,
I undersigned Ashok.Vadithya working with Dr.Reddy’s Laboratories Ltd, Bollaram, and
Hyderabad. Beg to apply for a suitable post in Quality Assurance in your esteemed
organization. If any opportunity is given, I am sure that I will work hard & on my experience
knowledge I will win your faith soon. I am enclosing here my resume which is true to the
best of my knowledge.
Thanks & Regards
(Ashok.Vadithya)
Date: - 22-12-2016
Place: - Hyderabad, Telangana.

2. CURRICULAM VITAE
Ashok.Vadithya
H.No: 3-81, Cell: 09666387130, 09491328733
Megyathanda,
Nidumanur, Email: ashok.vadithya@gmail.com
Nalgonda-508207
OBJECTIVE:
To initiate a career in growing pharmaceutical organization where enhancement of
knowledge is a continuous process. Will to work as a team in specific department so as to
achieve new milestone for the organization.
EDUCATION:
Degree/ Exam Board/University Institution
Year of
Passing
Percentage
M.Pharma
(Pharmaceutics)
Osmania University’
Hyderabad.
Nalanda College Of
Pharmacy.
Nalgonda.
2010-2012
75.21%
B.Pharmacy
J.N.T.U, Hyderabad MITS college of pharmacy.
Kodad, Nalgonda
2006-2010
68.61%
Inter (BiPC)
Board of Intermediate
Education,A.P
G.V.R&S college.
Guntur.
2003-2005
87.3%
SSC Board of Secondary
Education, A.P
A.P.T.W.R. School
Miryalaguda, Nalgonda.
2002-2003 81.6%
EXPIRIENCE:
Mylan Laboratories Ltd (Formerly known as Matrix Laboratories Ltd).
Location: Sinner, Malegaon MIDC; Nasik (Maharashtra).
Duration: May-2013 to Dec-2016.
Job Title: Officer in QA Dept.
Job Responsibilities: IPQA Activities and BMR Compliance.
Dr.Reddy’s Laboratories Ltd.
Location: Hyedrabad
Duration: Dec-2016 to till now
Job Title: Asst.Manager in QA Dept.

3. JOB RESPONSIBILITIES:
 To perform in process quality assurance (IPQA) activities in various areas of
operations and certify line clearance, in order to ensure cGMP compliance.
 Random in-process checks for verification, Log book verification, Pre dispatch
inspection, SNAP Audits, IQA etc.
 Check for adherences to QSP/MFR during manufacturing process.
 Issue of BMR, BPR after receipt of shop and Verification, retrieval and maintenance.
 To perform the testing of physical parameters of product.
 To perform sampling of in process, finished product and Hold time as per the product
BPCR or approved protocol.
 To monitor the qualification and validation activities, Implementation and Co-
ordination for validations.
 To withdraw control, stability, micro, Bio study and customer samples of the finished
product.
 To perform calibration of instruments used in IPQA labs and ensure the execution of
calibration schedule.
 To investigate and report deviations, changes, incidents, observed in various areas of
operations.
 To review the BPCR and completion of BPCR index.
 To perform SAP transaction as per requirement.
 To coordinate with engineering deportment for external calibration of IPQA
instruments.
 To perform sampling and monitoring of the cleaning process.
 Ensuring in-process instruments calibration, On-line inspections and on the job
training, Compilation of data for annual product review.
REGULATORY AUDIT EXPOSURE:
WHO
MHRA
Mylan GQA
USFDA

4. CRITICAL DELIVERABLES:
 An ability to work independently, as well as a member of a team in a dynamic, fast-
paced environment.
 Strong commitment to individual and team development with particular emphasis on
delivery of Quality Training.
 Knowledge of current Good Manufacturing Practices, ICH, quality systems and
quality assurance is required, along with working knowledge of manufacturing
process steps and quality control for Generic, biologics/ Biosimilars products.
 To ensure that facility is ready at all time to handle any of the regulatory. Customer,
etc., audits. To ensure the timely and effective closing of all such audit observations
and non-compliance.
 Ability to diplomatically enforce Quality expectations. .
INSTRUMENTS HANDLED:
Disintegration Test Apparatus, Hardness tester, Friability Tester,
HPLC (Agilent 1100), HPLC (Waters), GC (Agilent 6890), PH meter, UV-Visible
spectrophotometer ( PerkinElmer, Varian )
PERSONAL DETAILS:
Name in full : Ashok.Vadithya
Fathers Name : Dasaratha.V
Date of Birth : 21-10-1986
E-mail id : ashok.vadithya@gmail.com
Languages known : English, Hindi, Telugu
Hobbies : Listening music, Reading Books and Playing Chess.
PERSONAL ATTRIBUTES:
Quick to learn, confidence in doing things, hard work, commitment and integrity
towards achieving the goals, good logical thinking and analytical skills, finding creative and
innovative solutions and showing enthusiasm in knowing and learning new things.
DECLARATION:
I, hereby, declare that the above information furnished is true to the best of my
knowledge and belief.
Date: 22-12-2016 SIGNATURE
Place: Hyderabad. (ASHOK.V)