This document provides a summary of an individual's qualifications and experience in quality assurance. The individual has nearly 10 years of experience in quality assurance roles covering areas like auditing, inspections, process improvements, and laboratory operations in the diagnostics and medical fields. They currently work as an Assistant Manager of Quality Assurance and have expertise in implementing quality control systems, monitoring quality, and enhancing operational efficiency through process optimizations.

1. PERSONALITY TRAITS
Excellence in Analysis
Problem Solving
Commercially Aware
Optimizing Performance
Oriented Team Builder
Persuasive Communicator
SYED BASHEER UDDIN
Mobile No.: 9502095356 ~ E-mail: basheer.lucid@gmail.com
ASPIRING FOR SENIOR LEVEL ROLES IN:
Quality Assurance ~ Process Improvements ~ Laboratory Operations
~ Solid communication skills with the ability to contribute as a team player and interface with professionals at all levels ~
A BRIEF SNAPSHOT
Senior Quality Assurance Engineer with experience of nearly 10 years in Quality Assurance,
Auditing & Inspections, Continual Improvements, Laboratory Operations, Process Optimization
and Team Management covering Diagnostics / Medical domain. Presently associated with Lucid
Medical Diagnostics Pvt. Ltd., Hyderabad as Assistant Manager - Quality Assurance. Presently
associated with Canara Hydraulics Pvt. Ltd., Bangalore as QA Engineer. Skillful in monitoring
quality control in various operations, implementing systems for improving processes and
enhancing operational efficiency. Adept at developing, implementing & managing quality control
systems designed to ensure continuous production of advanced composite materials and
applications (consistentwith established standards,customer specifications and production goals.
Adept at managing the spectrum of activities in laboratory operations spanning testing, quality
control and coordination with cross-functional departments; developing & reviewing Laboratory
Quality Manual, Quality System Procedures & Standard Operating Procedures. Possess solid
managementskills and the abilityto analyze issues,devise continuous process improvements and
incorporate initiatives to increase efficiency, streamline operations and decrease overall expenses
with minimal resources.
SPHERES OF EXCELLENCE
Quality Assurance Laboratory Operations Auditing & Inspections
Technical Documentation Calibration Process Reengineering
Customer Relationship Management Defect Analysis Team Management
PROFESSIONAL EXPERIENCE
Since 2009: Lucid Medical Diagnostics Pvt. Ltd., Hyderabad as Assistant Manager - Quality Assurance
2007-2009: Jaferia Hospital, Noor Khan Bazar, Hyderabad as Senior Lab Technologist
2007-2009: Princess Dureshawar Hospital, Purani Havelli, Hyderabad as Senior Lab Technologist
Key Result Areas:
 Taking stringentquality measures including preparation ofnecessary documents to ensure compliance with above standards &
customer requirements
 Conducting internal audits (NABL audits) periodically to assess the status of deployment of systems and taking corrective
measures for achieving organizational objectives
 Accountable for:
o Ensuring corrective actions are taken for any non-compliance work; documenting preventive actions
o Issuing policies & procedures to the lab staff and ensure current versions of procedures are in place for usage
 Overseeing wide gamut of tasks involved in laboratory operations; handling calibration of lab equipment
 Ensuring adherence to quality standards; implementing & monitoring QC lab safety standards & undertaking quality data entry
and record keeping
 Reviewing SOP’s/technical specifications /batch manufacturing record /validation protocols, validation reports and other quality
documents
 Maintaining quality standards, ensuring stringent adherence to quality standards, norms & practices, identifying gaps & takin g
corrective action; enrolling for proficiency testing material and ensuring timely participation of PT evaluations
 Providing suggestions for novel approaches; designing lab processes to the lab managementand assisting in the implementation
of these approaches
 Responsible for identifying,documenting and reporting findings;communicating the findings to the Auditee, Head of the Division
and Quality Manager, where resolution of audit findings is inadequate
 Receiving EQAS/ILC sample; also maintaining chain of custody; reviewing & forwarding results to EQAS/ILC provider
 Actively involved in:
o Issuing forms, log books, SOPs and document of external origin to CRL
o Reviewing quality indicators logs, IQC summary and SOP master list
o Compiling data and generating graphics from the same
 Instituting corrective & preventive actions, as a result of internal/external audits and continuous improvement process, ther eby
ensuring their implementation
 Partnering with customers,third party auditors,EQAS/ILC providers and accrediting bodies; reporting EQAS samples from CAP,
AIIMS, etc.
 Reviewing external PT reports in consultation with HOD; also entering QC values in Unity software, review of IQC data and
taking appropriate corrective actions in case of QC failure

2.  Creating validation/verification protocols and performing the validation experiments
 Participating in performing maintenance and calibration of equipments & pipettes
 Directing, leading & motivating workforce and imparting continuous on job training for accomplishing greater operationa l
effectiveness/ efficiency
 Working on succession planning ofthe workforce, shiftmanagementactivities,appraising the member’s performance & providing
feedback
ACADEMIA
Pursuing Bachelors in Science - MLT
NIIMS University (3 years)
Professional Trainings & Certifications:
 Result Awaited: Advanced Diploma Quality Management Certificate
 Medical Lab Technology from Medwin Hospital, Hyderabad 2005 - 2007
 4-day training programme on “Laboratory Quality Management & Internal Audit as per ISO 15189: 2007” during Jul’11
 Workshop on EQAS Interpretation organized by Bio-RAD Laboratories during 26th
Aug 2011
 Participated in training program on the “Use of BD vacutainers Blood collection System”
 Quality Awareness Program organized by Bio-Rad Laboratories; the topics covered were Comprehensive QC: Basics of QCs,
Westgard rules and Technical Applications
 “EQAS Report Interpretation” conducted by Bio-Rad Laboratories India Pvt. Ltd. during 2nd
Mar13
 Trained on instruments viz. Clinitek Status and M 680 Elisa Reader,Rapid Chem 77 Electrolyte Analyzer, Advia 2120i Automated
Hematology Analyzer, Vesmatic 20 (Sedimentation) Instrument, Siemens Dimension Xpand Plus Fully Automated Clinical
Chemistry Analyzer, Sysmex CA-50 (Coagulation) Instrument, Abbott Axsym Fully Automated Immunoassay, BN PROPEC Fully
Automated Plasma Protein Analyzer, Hematology Automated Analyser Mindray BC-2800, Use Operations on & User
Maintenance of the Instrument EM 200 Clinical Bio-chemistry Analyzer
 Laboratory Information Management System (Powered by Athentech India Pvt. Ltd.)
 1-day training programme on Laboratory Accreditation, Requirements of ISO 15189:2012, Quality and Quality Management
Concepts, Difference between ISO 15189:2012 & 2007 Editions, Additional Requirements o f ISO 15189: 2012 Over & Above
Those Required by ISO 15189: 2007, Combination of Interactive Workshops and Discussion Tutorial on 21 st
December 2013
 CAP & BD Seminar on Calibration & Linearity Verification during February 2014
 Quality Forum for Bench Technologists Phase-1 Hyderabad organized by Bio-Rad
 Laboratories (India) Pvt. Ltd at Care Hospital OP Centre on 10th of January 2015
 Seminar on Advancing Quality & Outcomes organized by Becton Dickinson on 21st
April 2015
 Workshop on Risk Managementin Clinical/Medical Laboratoryorganized by Bio-Rad Laboratories (India) Pvt. Ltd., in association
with Dept. of Laboratory Medicine Care Hospital, Hyderabad on April 2015
 Has completed the one hour webinar entitled: Risk-Based QC for Clinical Laboratories on May 2015 Sponsored by Bio-Rad
Laboratories (I) Pvt. Ltd.
 1-hour webinar entitled: IQCP: Performing the Risk Assessment on 2nd
June 2015 sponsored by Bio-Rad Laboratories (I) Pvt.
Ltd.
 1-hour of P.A.C.E. Creditat the Louisiana POC Webinar:Lab Competency Assess ment Program on 16th
June 2015 Sponsored
by Professional Acknowledgment for Continuing Education
 Participated in CME on Basic QC Concepts,Technical Application,Westgard Rules, Optimum Use in IQC & EQAS Interpretation
on 18th
June 2015 Bio-Rad Laboratories (I) Pvt. Ltd.
 1-hour of P.A.C.E. Credit at the San Diego POC Webinar: Antibiotic Resistance: The Case for Diagnostics to Help Direct
Therapy on 23rd
June 2015 Sponsored by Professional Acknowledgment for Continuing Education
 Operator Training Course on Siemens ADVIA 2120i-Fully Automated 5 Part
 Hematology Cell Counter on 6th
August 2015 Siemens Healthcare Diagnostics Ltd.
 1-hour of P.A.C.E. credit at the POC Arizona IQCP Webinar on 9th
September 2015
 1-hour Webinar on The Impact of Poor Quality on the Lab Budget on 16th
September 2015, Sponsored by Bio-Rad Laboratories
(I) Pvt. Ltd.
 1-hour of P.A.C.E. credit at the Alere Webinar: Creating Your IQCP for Microbiology: Real Life Examples on 6 th
October 2015,
Sponsored by Alere Medical Education
 1-hour of P.A.C.E. credit at the Bio-Rad Webinar: Integrating the Cost of Quality into Laboratory Operations – 2nd
December
2015, Sponsored by Bio-Rad Laboratories (I) Pvt. Ltd.
 1-hour of P.A.C.E. creditat the San Diego POC Webinar:“Reducing Errors atthe POC: Keeping ‘Humans’ and ‘Error’ Apart”, 21st
January 2016, Sponsored by Professional Acknowledgment for Continuing Education
 AACC ACCENT Webinar at the Washington on “Cultivating a Culture of Quality in the Laboratory, 12th March 201 6, Sponsored
by American Association for Clinical Chemistry, Inc. (AACC)
 1-hour of P.A.C.E. Credit at the Heart of America POC Webinar: “What to do with Proficiency Testing”, 22nd March 2016,
Sponsored by Professional Acknowledgment for Continuing Education
 Actively participated in the training program cum hands -on workshop titled “Method Validation & Verification” at Aditya Park
Hotel, Hyderabad, 26th
March 2016, Sponsored by Value Added Corporate Services (P) Ltd.
 1-hour of P.A.C.E. Credit at the 3Rivers POC Webinar: “Quality Management-Making it Meaningful”, 28th
April 2016, Sponsored
by Professional Acknowledgment for Continuing
 Participated in AACC ACCENT Webinar at the Washington on “Accountable Care and the Laboratory Value Proposition”, 4 th
May
2016, Sponsored by American Association for Clinical Chemistry, Inc. (AACC)
 Educational Activity entitled “HIV Testing Update” and awarded 1.0 contact hours of continuing education credit
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