CURRICULUM VITAE

J.VENKANNA,
H.No: 13-9-1/2/37/2,
Ganeshnagar,
Borabanda, Ph: 9032585604
Hyderabad – 500018. Email: venkannaj2000@gmail.com

OBJECTIVE:
To pursue a challenging and innovate carrier in the emerging field by being associated
with a progressive organization, use my education and knowledge. Prove myself as one among
the best and asset for the organization.

EDUCATIONAL QUALIFICATION:
• Master of Arts ( M.A- English literature ) perusing from Acharya Nagarjuna University from
2008 – in distance mode.
• Master of Science (Analytical Chemistry ) 57% from Acharya Nagarjuna University from
2006 – 2007 in distance mode.
• Bachelor of Science (B.Z.C ) 67% from Andhra University from 2002 – 2005.
• Intermediate (Bi.P.C) 54.4% from Board of Intermediate education from 1999 – 2001.
• S.S.C 68% from Board of Secondary Education in March – 1999.

TECHNICAL SKILLS:
• Os −Windows 98/2000/2003/XP
• MS – Office
• Adobe Photoshop
ACHIEVEMENTS:
• Attend several GMP training programs. Periodically internal training programs conducted by
external consultants with the latest development with cGMP.

WORK EXPERIENCE:
 Working as a QA Chemist for UNI SANKYO LTD, injectables in Unit-II in QA
department from Oct 2006 to till date.

RESPONSIBILITIES:
• To ensure that product quality is secured all the time by control over production, QC, Stores,
and Engineering dept. To ensure that work is going as for cGMP.
• Issueing and follow up of BMR’s, BPR’s, Test / Analytical / protocols and Log Records to
the respective departments.
• Maintaining process records online along with daily documents.
• Online monitoring of BMR/BPR completion & other related GMP records in production.
• Collection of samples (product samples, WFI, purified water (DM water) and send them to
QC for analysis.
• Performing In-process quality checks in the departments during manufacturing and to give
line clearances for the critical operations
• Collection and Maintenance of Control Samples.
• Monitoring and Execution of real time stability studies and Stability evaluations.
• Management of Stability samples of new & existing products..
• Development, Implementation, Review and Verification of Standard Operating Procedures,
Analytical Protocols and Log Records.

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• Preparation of training materials and presentations.

• Review of process and batch data to provide appropriate OQ and PQ acceptance criteria.
• Review and verification of completed BMR’s / BPR’s received from production prior to release.
• Preparation & Issue of PRS’s.
• Monitoring of personnel hygiene, cleaning & disinfections of areas with respect to Production,
Stores, QC lab, Bio lab & Microbiology lab.
• Verification and approvals for Art works, Shade cards.
• Monitoring of storage practices for RM / PM / IP& FP for its compliance.
• Simplification and Redesign of documents.
• Execution and monitoring of GLP, GMP and cGMP guidelines in shop floor.
• Corrective and Preventive Action (CAPA),
• Quality Management and Quality Systems Development.
• Visit to the internal audits in the divisional manufacturing sites for facility/quality and GMP
Compliance.
• Monitoring validity periods for equipment calibrations / validations / volumetric solutions /
standard weights / working standards in production / stores & QC departments.
• Performing validations periodically, Equipments validation, Water system validation
(Distilled water, DM water and Steam), Product validations, Cleaning validation and Process
validations.
• Preparation of master schedules for calibration, validation, stability studies samples
collection & market surveillance programs.
• Plan for Internal self inspections of all departments as per Self Inspection Schedules.

M/S UNI SANKYO LTD, Hyderabad, a joint venture with Dhiichi sankyo ltd-japan.

Company Profile:
UNI SANKYO LTD, Hyderabad approved by WHO & ISO 9001-2000 Certified
Company its production and R&D facilities located at Gaganpahad Industrial Area, Shamshabad
mandal, in R.R District of A.P. To meet the challenges, Uni sankyo has established vibrant,
proactive QA and QC departments.
(Our UNIT-II involved in the formulation of injectables).

 Worked as a Technical Assistant for UNI SANKYO LTD, Injectables (formulation

division) in production department from 5th Oct-2005 to Oct 2006.

SKILLS:
• Knowledge of US FDA regulations.
• Quality System Inspection Techniques (QSIT).
• Quality System Regulations (QSR).
• Knowledge of schedules-M,U&T
• GMP guidelines.
• WHO guidelines.

STRENGTHS:
• Effective communication skills reliable.
• Hardworking and quick learning.
• Ability to manage multiple tasks simultaneously.
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• Good level of self confidence.

PERSONAL DETAILS:
Name : J.VENKANNA
Father name : Venkata Ramarao
Date of Birth : 20th August 1983
Marital status : single
Nationality : Indian
Religion : Hindu
Languages known : Telugu, English & Hindi.

Permanent address : J. Venkanna,

S/o. Venkata Ramarao,
Satyanarayana nagar,
Mulalanka ( post ),
Kalidindi ( mandal ),
Kaikaluru(TQ),
Krishna ( Dist ),
Pin – 521344.

DECLARATION:
This is certify that the above mentioned information is true and genuine to the best of my
knowledge.

Date:
Place: Hyderabad. (J.VENKANNA)

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