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Document Name: Quality Assurance Procedure

Document Number: QMS/QA-P/01

Quality Assurance
Procedure
V1.0
DOCUMENT INFORMATION

Document Name Quality Assurance Procedure


Document No. QMS/QA-P/01
Version No. 1.0
Abstract Procedure for Quality Assurance

DOCUMENT REVIEW HISTORY

Version Date Prepared by Reviewed by Changes / Reasons for Authorized by


change
1.0 06.01.2020 EPG Team Kumar Amit Released Version Ratan Sah

Quality Assurance Procedure [QMS/QA-P/01] Page 2 of 6


TABLE OF CONTENTS

1 PURPOSE 5
2 REFERENCE DOCUMENTS 5
3 ABBREVIATIONS AND ACRONYMS 5
4 ROLES AND RESPONSIBILITIES 5
5 PROCESS DESCRIPTION 5
5.1 ENTRY CRITERIA 5
5.2 INPUTS 5
5.3 ACTIVITIES 6
5.3.1 Develop quality assurance plan 6
5.3.2 Conduct process audit 6
5.3.3 Conduct work product audit 6
5.3.4 Record and Track non-compliance (NC) issues 6
5.3.5 Suggest Process Improvement 6
5.4 VERIFICATION 6
5.5 OUTPUTS 7
5.6 EXIT CRITERIA 7
6 MEASUREMENTS 7
7 TEMPLATES USED 7

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1 Purpose

The purpose of Quality Assurance (QA) is to provide staff and management with objective
insight into processes and associated work products.

2 Reference Documents

● Project Plan
● Process Compliance Checklist
● Work Product Audit Checklist

3 Abbreviations and Acronyms

QA - Quality Assurance

4 Roles and Responsibilities

Role Responsibilities
QA ● Prepare the QA plan and schedule
● Conduct Audit
● Prepare Non Compliance list
● Communicate with concern department
● Monitor & review Non Compliance list

5 Process Description

5.1 Entry Criteria


Entry Criteria for Quality Assurance Procedure are listed below:
● Project has formally started
● QA role has been assigned

5.2 Inputs
● Project Plan
● Customer requirement related to quality, standards, etc.
● Defined Procedures

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5.3 Activities

5.3.1 Develop quality assurance plan


QA make a quality assurance plan at organization/project level and develop schedule for
the same. Refer to tailoring guidelines at project level.

5.3.2 Conduct process audit


As per plan and defined procedures, QA conduct process audit where it objectively
evaluates performed processes against applicable process descriptions, standards and
procedures (using process compliance checklist).

5.3.3 Conduct work product audit


As per defined audit checklist, QA conduct work product audit for objective evaluation
of performed processes against applicable process descriptions, standards and
procedures (using work product compliance checklist)

5.3.4 Record and Track non-compliance (NC) issues


If activity does not comply with defined procedure, QA record in NC list and track till NC
is closed.

5.3.5 Suggest Process Improvement


QA make continuous effort to understand the process effectiveness in the project &
organization and suggest process improvement to process management group (EPG).
Following techniques should be utilized to understand potential improvement:
● Suggestion by process users during process & work product audit
● Understanding on procedure & template by process users
● Non-compliance trend across procedure & projects
● Closing of NC and improvement of process.

5.4 Verification
● Quality Assurance Plan is reviewed along with project plan.
● Resolution of Non-compliance items for appropriateness & corrective action is
reviewed with EPG.

5.5 Outputs
● Process Compliance Checklist (Filled with result)
● Non-compliance list
● Process improvement suggestion

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5.6 Exit Criteria
● QA plan implemented successfully

6 Measurements

● Number of NCs found, open & closed

7 Templates used

● QA Plan – EPG_QA_TRNG (QMS/QA/01)


● QA Plan – Work Products (QMS/QA/02)
● Review Report (QMS/PE/14)
● Non-Compliance Report (QMS/IA/04)
● Process Improvement Suggestion List (QMS/Process/04)
● Process Compliance Checklist (QMS/QA/03)
● Work Product Audit Checklist (QMS/QA/04)

--- End of Procedure ---

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