Venkata Prasad Vemulapally has over 11 years of experience in pharmaceutical quality control and quality assurance. He currently works as an Executive Quality Operations at Mylan Laboratories Ltd, where he is responsible for reviewing chromatography and chemical analyses to ensure compliance with cGMP and USFDA regulations. Previously, he worked as an Analyst in Quality Control at Divi's Laboratories Ltd, where he performed instrumental and chemical analyses of raw materials, intermediates, and finished products. He has extensive experience with HPLC, GC, UV-Vis spectroscopy, FT-IR, and potentiometric titration instruments. Vemulapally holds a Master's degree in Biotechnology and Bachelor's degrees in Chemistry, Botany, and

1. VENKATA PRASAD VEMULAPALLY
Myprasad6666@gmail.com
9676965781
Profile snapshot:
About 11 years of experience in the pharmaceutical analysis of API and documentation
as per USFDA & cGMP. Analysis of both instrumental and chemical of all the finished
products, Intermediates, inprocess and Raw materials. Seeking for challenging position
in Quality control and Quality assurance.
Professional Experience:
 Working organisation: MYLAN LABORATORIES LTD.
 Duration. :. October2006 to till date I am working here.
 Designation. : Executive Quality operations.
 Department. : Quality control.
Responsibilities:
Working as reviewer for both chromatography and chemical analysis. Responsible to
check all the things in QC lab which will effect cGMP and ensure the online
documentation as per US-FDA.
Responsible to check sequence, method of analysis and all other parameters which will
effect the chromatographic analysis (HPLC&GC) before starting the analysis. And
verification of integration and custom field calculations after completion of analysis.
Verification of analysis completed batches then review and ensure releases the same
through SAP. Handling of OOS, OOT, and Change control. Responsible to monitor the
equipment log books and records. Ensure periodic calibration of instruments, review
and maintenance of calibration data. Helping junior colleagues in trouble shooting of
Instruments and coordinating with service engineers to rectify the problems.
Responsible to give GLP & Core SOP s trainings to team members.
Previous Experience:
 Working organisation: DIVI's LABORATORIES Ltd.
 Duration. : March-2005 to September 2006.
 Designation. : Analyst Quality control.
Responsibilities:
Responsible for analysis of Raw materials, Intermediates & finished products.
Responsible for analysis of both Instrumental & chemical analysis. Responsible for
preparation of volumetric solutions & standardizations. Responsible for daily calibrations
of Analytical balance, PH meter & KF standardizations. Responsible to ensure lab
cleaning & glassware cleaning. Following good laboratory practices in the department.

2. INSTRUMENTS and Software’s HANDLED:
Network Systems Waters, Agilent and Shimadzu HPLC connecting with Empower-3
software.
Models are alliance 2695, Agilent 1200 series, and shimadzu prominence.
Agilent GC connecting with Empower-3 software
Models are 6890N, 7890A, 7890B connecting with 7694E& G188 HSS systems.
Metrohm Potentiometer, Karl Fischer titrations and coulometry.
UV-Spectrometer with PerkinElmer Lambda 35 UV Winlab 6.3.2 software.
Fourier Transform Infrared Spectrophotometer (FT-IR) with
Data handling system of Perkin Elmer spectrum ES.
All systems incorporated with audit trail review by us.
Skills:
 Proven skills in Review, planning and effective utilization of resources.
 Rich problem solving capability. Ability to lead team under pressure situations to
meet deadlines. Ability to work independently as well as team player and team
leader.
 Knowledge on ICH guidelines and pharmacopeia’s.
 Excellent knowledge on Calibration & Trouble shooting of instruments handled.
Having very good practical & theoretical knowledge on chromatographic,
spectroscopic techniques and on column chemistry.
 Knowledge on method transfers, validations and developments.
Trainings and Special features:
Undergone training conducted by Waters and got the certificate of attendance from
LIQUID CHROMATOGRAPHY SCHOOL conducted by Waters. Got Training on general
core SOP s. attended various seminars on Chromatography, Spectroscopy by different
manufacturers.
Participated in three USFDA, TGA, WHO & Mexican Regulatory and other regulatory
audits. Expertise in documentation as per USFDA and cGMP Guidelines.
EDUCATIONAL QUALIFICATIONS:
Master degree in Science Biotechnology from Ramanand teerth Marathwada University,
Nanded in 2003.
Bachelor of Science Chemistry, Botany and Microbiology from Osmania University in
2001

3. Personal Information:
Name. : Venkataprasad Vemulapally
Father s Name. : Gangadhar Rao.
Date of birth. : 23-03-1980.
Marital Status. : Married.
Languages known : English, Telugu, Hindi
Nationality. :. Indian.
Communication address: .Plot no 39 &40,
Bolaram railway station, Hyderabad
Declaration: Above mentioned subject is truly correct and it is my knowledge and
experience.
VENKATA PRASAD VEMULAPALLY