Phone: +919866032165
To
The Manager, HRD
Sub: Application for suitable position in your esteemed organization.
Respected Sir/Madam,
I Pathapati Rangarao have completed my B.Pharmacy from Dr.MGR Medical
University (Chennai). I am writing this letter for your kind consideration regarding
suitable post in your esteemed organization. I am interested to serve your organization in
order to expand my knowledge levels.
If you will be given an opportunity, I will work with dedication to contribute my fullest
for the growth of your organization. I wish you kindly oblige and consider my application
favourably.
Thanking you
Yours faithfully,
(Pathapati Rangarao)
CURRICULAM VITAE
Pathapati Rangarao,
Summanpadu post,
G.konduru mandal,
Krishna district,
Andhrapradesh- 521229. OBJECTIVE:
To start my career in a reputed company in the position, which will give me the space to
grow and enhance my potential which i can contribute to the organization using my current
knowledge and qualification to the maximum possible level.
Overview
10
10
years of professional experience
Work History
Senior Executive
Aurobindo, pharma limited
10.2020 - Current
As a team member I was responsible for
To ensure drug product is correctly processed, checked according to defined standard
operating procedures
Responsible for carry out start up and in process checks during manufacturing and
packing activities
Sampling of in process finished products, reserve samples and stability samples, in
packing activity
Responsible for giving of line clearance to granulation, compression, coating,
inspection and packing areas
Review online and complete batch manufacturing records for completeness its
compliance to coordinate for batch release
Preparation of COC, COM certificate for batch releases
Sampling of process validations, hold time study samples, cleaning validations
samples, stratified samples submission to QC
In-process checks of compression, capsulation, granulation, coating and primary,
secondary packing activities
Ensure the samples scanning to track and trace
Ensure implementations of cGMP
Batch manufacture record, Batch packing record review
Samples registration of LIMS, BMR approval in DIMS
Responsible for review of deviations, incidents, change controls
Review of QA and other relevant department sops
Review of MMFC and MPFC
Review of log books
Review of retention samples
Sharing of batch related documents to customers and related queries
Critical process parameter data entry in Process pad application
Responsible for QC released batches to dispatch
Performing AQL after completion of compression, coating, capsulation and release
for approval
During Equipment qualifications performing sampling as per qualification protocols
submission to Q.C, As a part of B.Pharmacy
Title:“Design and charecterisation of Mucoadhesive films of Felodipine buccal patches
delivery” thesis submitted to Dr.MGR Medical University.
Senior Executive in Production Department at EUGIA PHARMA SPECIALITIES UNIT -III (AUROBINDO PHARMA LIMITED(unit-IV) )Senior Executive in Production Department at EUGIA PHARMA SPECIALITIES UNIT -III (AUROBINDO PHARMA LIMITED(unit-IV) )
Dy. General Manager-International Regulatory affairs at Aurobindo Pharma LimitedDy. General Manager-International Regulatory affairs at Aurobindo Pharma Limited