Raju dokkara +48729459715

rajudokkara33@gmail.com
Pharma Quality assurance professional

Professional Summary

• Results oriented Quality assurance (QA) specialist well experience in

pharmaceutical industry including Knowledge on Quality system documents,
regulatory documents and CGMP documents.
• Proven track record of success in administering quality systems and Expertise in
improving quality systems.
• Knowledge of C-GMP, GDP, GLP, QMS, CAPA, regulatory and guidelines.
• Proven leadership skills with the ability to provide guidance to Jr. staff to achieve
goals.
• Strong training skills in CGMP and SOP’s.
• Expertise in auditing as per FDA and ISO and Participated as Team member in
number of Regulatory & Customer audits, Central Drug Standard Control
Organization (CDSCO, DCA Govt.of India) Audit, USFDA Audit and ISO Audit.
• Goal oriented and result driven team leader,tolerant patient with the people.

Technical skills summary

Microsoft Excel | outlook | PowerPoint | word

Professional exposure Laboratory information management system

Career history

• Working with Vandana life sciences pvt ltd. as Sr.Executive- Quality Assurance
from July 2019 to till continuing
• Worked with Analys lab Pvt.Ltd(Hetero group) as Executive-Quality Assurance
from May 2017 to June 2019
• Worked with Vasudha pharma chem ltd.as Exective- QualityAssurance from Feb
2014 to May 2017.
• Worked with JPR labs pvt ltd as Chemist-Quality Assurance from May 2012 to
Feb 2014.
• Worked with Sri sai agri bio labs as Microbiologist from August 2007 to March
2012

Responsibilities
• Handling of change control,deviation,Incident,Out of specification, complaints and return
goods
• Preparation and Review of validation protocols and validation reports
• Handling of Internal audits & Trainings as per Schedule.
• Reviewing of completed Batch production record & Analytical rawdata.
• Filling vendor questionaries’and checking vendor Qualification.
• Coordination with External Audits and Audit compliance.
• Preparation and review of SOP’s
• Reviewing of BPCR & STP as per technology transfer documents for batch execution
• Review of Method development/validation/verification/transfer.
• Prepration and review of Annaul Product Quality review (APQR).
Raju dokkara +48729459715
rajudokkara33@gmail.com
Pharma Quality assurance professional

• Partcipated in commercial dispatch activities and QA Release.

• Involving in line clearance activities.
• Responsible for Issue, retrieval, archieval and distribution of documents, on line
documentation and focus on data integrity.

Education

• Masters in microbiology from Andhra university,India

References

• References provided upon request