Naresh Pakerla
Quality control officer
PERSONAL INFO
Contacts
C/O. A.JAYAPRADA,
H.NO.48-579/1/303,
GANESH NAGAR,
QUTHBULLAPUR (MD)
RANGAREDDY (DIST),
Hyderabad-500054
Phone-9700321542
E-mail
naresh.pakerla@gmail.com
TECHNICAL SKILLS
Operating system:
Windows 03, 07, 08.
MS WORLD:MS Word,
MS Office, MS Excel,
Power point presentation.
OTHER TRAININGS
Attended training for
First aid.
Attended training related to
Fire fighting.
Attend the training for
waters and Agilent HPLC
trouble shooting
LANGUAGES
English, Telugu, Hindi
INSTRUMENTS HANDLED.
HPLC-Waters alliance with
Empower sofware-3,
Model2487, 2489
Shimadzu with Lab Solutions,
Model: 2010,2030,
Agilent -1220, 1260 series.
GC-Agilent(Model) Head space &
Auto Liquid injector
UV-Perkin Elmer, Agilent-8453
IR-Perkin Elmer
POLARIMETER -Perkin Elmer
KF AUTOTITRATOR -795 KFT
Titrando
SUMMARY
Quality control officer with 4+ years of experience in quality control department and
performing stability and finished product samples of API
EDUCATION
MSc
KGRL PG college affiliated by Andhra university.
BSc
SMBT Degree college affiliated by Andhra University.
EXPERIENCE
2015-06 Quality control officer
Till now Mylan laboratories ltd. (US FDA&WHO). Hyderabad
 Determination of Related impurities, purity and
Assay by HPLC and UPLC for stability samples.
 Analysis of Finished, stability, Raw materials and
Intermediates samples .
 Monitoring of stability studies and analyzing the
samples.
 Determination of Residual solvents by GC.
 Online documentation through the Laboratory
Information Management System(LIMS).
 Trouble shooting of HPLC and GC.
 Faced FDA and customer audits.
2013-12 Quality control chemist
To 2015-06 Gennex laboratories ltd. (ISO-9001-2008) and
(OHSAS-18001/2007) Hyderabad
 Handling of HPLC, GC, U.V& GC Head Space, ALS.
 Maintain & Analysis of Stability Studies as per ICH
Guidelines.
 Handling the Control (Retention)Samples
 Analysis of API’S, Intermediates, Raw materials
and in-process reaction monitoring.
 Qualification of working standards.
 Faced ISO 9001:2008,14001:2004 ,OSHAS 18001-
 2007& Customer Audits.
WORK EXPERIENCE
 Operation and Calibration of Analytical
Instruments as per Schedule.
 Maintenance of cGMP Records.
 Analysis of Working standard qualification.
 Following cGMP, GLP, Specification test methods
and Standard operating procedures.
 Reviewing of Analytical data.
 Fundamental Knowledge on method validation
And method verification.
 Knowledge about OOS, OOT, Deviation and
Incident & Change control.
 Follow the USP, EP, BP Pharmacopeia’s ,and
ICH Guidelines.