This document contains the resume of Balaprasad Peddi. It summarizes his contact information, objective, education, professional experience working for various pharmaceutical companies over 7 years in quality assurance, job responsibilities in his current and previous roles, an M.Pharm project experience, achievements in successfully passing regulatory audits, and personal details.

1. BALAPRASAD PEDDI
balaprasadpeddi@gmail.com
Address: H.No:54,55
Near: Beside swaroop Motors,
Madinaguda,
Miyapur,
Hyderabad (Telangana),
Phone : 9573706474,
9030574885
Objective:
To actively contribute to the development and growth of the organization where my programming and
communication skills could be utilized to the fullest extent and to achieve the remarkable position.
Education: Annamalai University, Chennai, India. May 2008.
M.Pharmacy-Quality Assurance with an aggregate of 7.5 Bands out of 10.
Jawaharlal Nehru Technological University, Hyderabad, India, April 2006.
B.Pharmacy, with an aggregate of 65% .
Professional Experience:
(Total 7 years of experience in Quality Assurance)
Aurobindo Pharma limited, Hyderabad
Sr.Executive Quality Assurance
June 2012 – till date.
Dr. Reddy’s Laboratories, Hyderabad
Junior Manager – Quality Assurance
April 2009 – May 2012
Cadila health care Limited,Goa
QA Officer May-2008-April 2009
Job Responsibilities at Aurobindo Pharma Limited:
Presently working as a shift in charge for Quality assurance department to monitor shop floor
Activities in tablet department Bachupally, Hyderabad, India.
• Responsible for In-process quality assurance activities & compliance of cGMP in
manufacturing.
• Team member of self-inspection audits committee audits and involved actively to perform
the internal audits.
• Responsible for training of newly joined employees, technicians, and ensuring timely
completion of training matrix of on job trainings.

2. • Monitoring all IPQA activities in TABLET BLOCK like Dispensing, Manufacturing, Filling and
Packing in Production department.
• Monitoring Validation batches and their reports for compliance.
• Ensuring Collection of Control, Validation, Stability and Reserve samples.
• Ensuring compliance of line clearance, In-process checks and review of batch records.
• Implementations of change control, Incident, Deviation and their Disposition.
• Coordinating to all the Internal, External and Regulatory Audits.
• Execution of Transport worthiness studies and ensuring the Data loggers as per
consignment.
Job Profile at Dr.Reddy’s:
Previously worked as a Junior Manager at Dr.Reddy’s Laboratories LTD, Quality Assurance
Department, Bachupally, and Hyderabad, India.
• To ensure that all manufacturing process associated with in the full compliance of GMP and
as per SOP.
• Carry out line clearances during manufacturing and packing operations for batch to batch
and product to product change overs.
• Doing Blend sampling for commercial and validation Batches and ensuring sampling at
different stages of semi-finished and finished products.
• Reviewing the batch records with respect to stage wise yield reconciliation, in-process
checks, sampling details, line clearance, manufacturing materials approved specimens.
• Ensuring the timely release of semi-finished and finished product COA’s in coordination
with Quality control department.
• Ensuring the timely dispatch of batches by coordinating with quality control and supply
chain and ware house departments.
• Performing self-inspections and ensuring compilation of non-compliances.
Job Profile at Cadila health care Limited:
Cadila healthcare limited, Goa plant manufactures drugs to ROW markets and domestic market.
I did my training in QA department of cadila plant. Trained all core areas of quality assurance
Which includes?
• Giving line clearances and doing in process checks in dispensing, Manufacturing and
packing areas of both tablet and injection blocks.
• Collection of semi-finished and finished product samples at different stages of
manufacturing process of tablets and injections.
• Preparation and compilation of process validation protocols.
• Collection of cleaning validation samples and compilation of cleaning validation protocols.

3. • Ensuring periodic validation of Autoclave and DHS.
M.Pharm Project Experience:
I did my M.Pharm project as part of M.pharm curriculum at Dr.Reddy’s Laboratories LTD, Biologics
development center, VALIDATION Department, Bachupally, Hyderabad,
Duration: June2007-April 2008.
Which includes?
• Preparation and Execution of facility validation Master plan.
• To carry out the qualification of equipment’s like Autoclave, DHS and Cold Storages.
• To carry out Area Qualification and Classifying the different classes of the clean rooms.
• To perform Qualification water systems which include Qualification of purified water and WFI.
• To performing media fill studies as per requirement.
Achievements:
 Success fully faced USFDA Audit in the month November 2011.
 Success fully faced MHRA Audit in the month August 2010.
 Success fully faced ANVISA Audit in the month December 2009.
 Success fully faced WHO Audit in the month April 2012.
 Success fully faced MCC Audit in the month June 2013.
Personal profile:
Name : Bala Prasad Peddi
Father’s Name : Balaiah.P
Date of Birth : 11-08-1983
Languages known : Telugu, Hindi and English
Mother Tongue : Telugu
Address : H.No: 1-5/c, Cherial,
Warangal,
Telangana, INDIA.
Pin Code: 506223.
Declaration:
I hereby declare that the above written particulars are true to the best of my knowledge and belief.
Place:
Date :

4. [BALAPRASAD.P]