Description - Paper - B - With ISO9001 - Revised (24!02!2024) )
Description - Paper - B - With ISO9001 - Revised (24!02!2024) )
Description - Paper - B - With ISO9001 - Revised (24!02!2024) )
Description items
1. Name and address of the person who prepared (Quality control manager) (Form number: 8211-04J)
2. Name and number of relevant JIS standard (Form number: 8211-05D)
3. Manufacturing or processing factory or business establishments
4. Organization chart (management structure) of manufacturing factory (including the entire company) and
descriptions of quality control manager, quality control committee, etc.
[Note] 1. The sheet of size A4 defined by JIS Standard shall be used for the all items and not stapled.
2. In the case that multiple manufacturing factories are included in the application, this paper shall
be drawn up per each factory.
3. The personal information notified by the applicant shall be used only for the purposes of business
contact and coordination concerning product testing/audit/certification, guidance of other
services which JQA implement, and provision of various information. However, on JQA's own
responsibility for the management of the personal information, the personal information notified
by the applicant may be used jointly between specific entities which accredit/register JQA.
Date of preparation:
Name of company and department : Nirmal Wires Private Limited – Deulti Unit
Name of person who prepared and title : Vineet Singh, QC Manager
Telephone number : 8335079204
Fax number :
E-mail : [email protected]
Name of factory concerning certification: Nirmal Wires Private Limited – Deulti Unit
[Associated factory] : NA
Name :
Address :
Contact person in charge :
Title or department :
Telephone number and e-mail address :
[Note] 1. The document describing the quality management implementation condition shall be drawn up by
the applicant as attachments to the application.
2. This document is prepared in the Word format. Please adjust yours to this format, if you use other
software.
3. The description paper shall be drawn up per each factory if multiple factories are
included.
4. Please delete unnecessary parts (such as “Note ”here, page, etc.) in this form when
preparing the description paper.
4. Organization chart (management structure) of manufacturing factory and quality control manager and quality control committee:
DIRECTOR
MANAGEMENT TECHNICAL
COMMERCIAL
Quality Control:
QCM
[Note] 1. Please draw the organization chart showing specifically the factory chief and the person in charge with number of personnel in each department.
2. Please describe the positions of the Quality control manager and committee on quality.
3. Please illustrate the relationship between the head office and the factory (including associated factory), when they are separately located.
4. Please delete unnecessary parts (such as “Note” here, page, etc.) in this form when preparing the description paper.
Management and person Title and department Major responsibility and authority
in charge
Mr. Pratap Ghosh General Manager - 1. Participating in the development of
Operations business policy, and supporting the president and
giving necessary advice
2. Production planning, and fulfilling them
after approved by president
3. Involving with the development and
implementation of safety and health standards,
pollution control policy, and crime/disaster
prevention policy
4. Performing special assignments from the
president, and assignments to be carried out on
his/her own responsibilities
Mr. Daleshwar Ram MR & Group HR 1. To perform various Human Resource
functions which includes delivering sustained
organizational growth, establishing structure,
driving vision and achieving critical strategic
goals.
2. To incorporate HR practices on cost
effective talent acquisition, training &
development, competency mapping, performance
management
3. Managing people at various levels,
maintaining healthy employee relations,
resolving employee grievances to create a
transparent environment
4. To Formulate and implement programs
designed to achieve strategic, business, and
operational goals; and advised senior leadership
on matters that include talent acquisition,
performance management, strategic planning,
policy, staffing, compensation, and succession
planning.
5. Maintaining effective employee relations
by guiding the employees in matters pertaining
to performance plans, conduct, manager issues,
salary, policies and so on
6. To develop organizational transformation
roadmap that includes all major efforts including
identifying and communicating risks, issues and
directors
4. Payment follows up
5. Sending Payment Update to vendors
6. Follow up materials dispatch
7. Discussion on daily basis work within team
8. Distribution of work within team.
Mr. Abir Chakraborty Incharge - Stores 9. Daily basis physical round at Packing materials
store, powder godown & Diesel godown
10. Raising Indent (average 25 item in a
days)
11. Entry of Material Issue in ERP (average
70 issue in a day)
12. Updation of Store Issue Book (average
70 entry in a day)
13. Getting printout of indent, obtaining
approval, scanning, sending to HO via mail.
(average 2 in a day)
14. Ensure loading & unloading of material.
(average 2 in a day)
15. Weighing of Wooden Drum (average 10
in a day)
16. Reconciliation of In & Out materials with
Accounts (Mr Manas)
17. Generation of Manual Gate Pass for
sending the items for repair & maintenance
(average 2 times in a weekly
18. New Item creation in ERP (average 6
times in a week)
19. Powder issue to Wire Drawing (Avg. 10
times in a month) Individual 5 times
20. Weighing of LPG Gas – every alternate
day (average 5 times in a month)
21. Materials Follow-up Meeting with
procurement dept. in every fry day
22. Daily basis report to Commercial head
regarding day plan & materials status.
Mr. Amber Jhunjhunwala Incharge - Dispatch 1. To obtain consent of Management for
Dispatch plan for a week and to provide the
same to Dispatch Coordinator to ensure at the
time of Dispatch it should be in ready
condition and also to its monitoring.
2. To circulate the Dispatch plan to “Unit II Group”
for arrangement and loading of the material.
3. To coordinate with transporter for vehicle
[Note] 1. Please itemize the major scope of responsibilities and authorities of each department manager
including quality control manager.
2. Please use the sheet of A4 vertically or horizontally. Please keep the column of “*” for JQA use.
3. Regarding Quality control manager, please refer to the item 5-b “Criteria for quality management
system”.
4 .Regarding the responsibility and authority of each department(manager), please put them of the
following person applicable.
1) top management
2) quality control manager
3) person in charge of manufacturing process
4) person in charge of purchasing (materials)
5) person in charge of subcontract control
6) person in charge of quality control
7) person in charge of shipment
5. Please delete unnecessary parts (such as “Note” here, page, etc.) in this form when preparing the
description paper.
(5) Agreement on viewing assessment reports when the registration under ISO9001 is
conducted by JQA.
We ask that our quality management system registered will be used for JIS certification
operation. Therefore, we agree that the assessment reports kept by JQA as related materials
for assessment & registration operation will be viewed.
for the condition of quality management including this form shall be prepared for each
assessment & registration.
2. Please write the registration status on the column (1) as to whether you have been certified
and registered.
If your quality system has not been registered, please put “not registered.”
3. Please describe the status of your quality manual in quality system on the column (2).
4. Whether your quality system has been registered or not, please attach your latest quality
manual.
Please attach the copy of certificate as well, if you got registered.
5. Please attach a copy of the internal standards equivalent to a product standard (for example,
specification which specify the performance etc.) and a product testing standard (for
example, testing regulation for confirming the quality required by JIS)
6. As for the column (4), please attach the copies of assessment reports for three times
including the latest, in the case that your quality system has been registered by an
organization.
7. As for the column (5), we ask you to write your signature to show your agreement on the
viewing, in the case that your quality system has been registered by JQA, however, the
attachment of the audit reports is not required.
8. Please delete unnecessary parts (such as “Note” here, page, etc.) in this form when
preparing the description paper.
(5) Annealing
(8) Galvanization
(10) Packing
(11) Shipping/PDI
[Note] 1. Please illustrate each process from the acceptance of materials to shipment by means of using
symbol specified in JIS Z 8206 and enter the process name and control points. It is possible to
attach the manufacturing process control table specified in the internal standards (for example,
QC Process Chart etc.).
2. Please draw up this paper relating the outline of condition of quality management shown in 6-3
(the same number by processes).
3. Please write any processes about subcontracting and associated factory as well. In addition, please
include identification symbols for these subcontracted processes.
4. Please delete unnecessary parts (such as “Note” here, etc.) in this form when preparing the
description paper.
Associated factory:
To entrust the whole or a part of manufacturing process, testing of products and/or calibration of
measuring instrument to the group companies where capital ties exist or to the other own
factories
[Note] 1. This document is prepared in the Word format. Please adjust yours to this format, if you use other
software.
2. Please use the sheet of A4 vertically or horizontally. Please fill in each column with necessary
numbers and keep the column with “*” for JQA use.
3. Raw materials, parts or sub-materials are to be entered into the column of “Name of materials,”
however, which can be limited to the materials specified in the relevant JIS standards and the
[Note] 1. This document is prepared in the Word format. Please adjust yours to this format, if you use other
software.
2. Please use the sheet of A4 vertically or horizontally. Please fill in each column with necessary
numbers and keep the column with “*” for JQA use.
3. As for the column of “Process name,” in principle, please describe the processes affecting product
quality among those specified in your internal standards including final inspection process.
4. Please put the identification mark in the case that a part of the processes is undertaken by the
affiliated companies or subcontractor.
5. As for the column of “Control items and quality characteristics,” please describe control items and
quality characteristics and their values specified in your internal standards.
Regarding control items, please describe items and their specified values that are under control
among factors that could affect quality such as temperature, pressure and the shake of principal
axis, etc.
As for the quality characteristics such as hardness, tension, etc., please describe the items of
them and their specified values.
6. As for the column of “Control and inspection methods,” please describe the control method
corresponding to the control items and inspection method corresponding to quality
characteristics among control and inspection methods specified in your internal standards. As
for control method, please describe frequency and time of control, size of samples and type of
control chart, etc. for each control item.
As for inspection method, please describe whether the inspection is conducted for all or samples
for each quality characteristic (in the case of conducting sampling inspection, size of lot (N),
number of sample (n), judging criteria for lot and handling of nonconforming lot, etc.).
7. It is possible to attach a copy of the control table on manufacturing prescribed in the internal
standards (for example, QC Process Chart etc. However, it needs to include items listed above in
the table or chart.)
8. If you could attach a copy of the internal standards such as “product standard”, “product testing
standard”, “in-process testing standard” and “shipping test standard”, it is possible to write down
only process name.
9. Storage term of quality records regarding JIS Mark products is needed for at least three years.
10.Please delete unnecessary parts (such as “Note” here, page, etc.) in this form when preparing the
description paper.
Crane
[Note] 1. This document is prepared in the Word format. Please adjust yours to this format, if you use other
software. It is possible to attach the list of facilities provided in the internal standards. However,
it needs to include items listed above in the list.
2. Please use the sheet of A4 vertically or horizontally. Please fill in each column with necessary
numbers and keep the column with “*” for JQA use.
3. As for the column of “Name of major manufacturing facility,” please describe the facilities
affecting product quality among those being used.
Please put each identification mark in the case that the major manufacturing facility is located in
the affiliated companies or subcontractors.
4. As for the column of “Control of facility,” please describe the points, items and cycle of major
check or inspection which your internal standards specify for each major manufacturing facility.
In the case that the operations of check or inspection are subcontracted, please put the name of
the organization undertaking the operations with brackets under the points and items of check or
inspection.
5. If you could attach a copy of the internal standards such as “facility control standard” or of the
document on outline of facilities in which the ability and specification can be found, it is possible
to write down only facility name.
6. Please delete unnecessary parts (such as “Note” here, page, etc.) in this form when preparing the
description paper.
[Note] 1. This document is prepared in the Word format. Please adjust yours to this format, if you use other
software.
2. Please use the sheet of A4 vertically or horizontally. Please fill in each column with necessary
numbers and keep the column with “*”for JQA use.
3. As for the column of “Name of major inspection (testing) facility,” please describe the facility
affecting product quality among those being used.
Please put each identification mark in the case that the major inspection (testing) facility is
[Note] 1. This document is prepared in the Word format. Please adjust yours to this format, if you use other
software. It is possible to attach the list of subcontracting provided in internal standards.
However, it needs to include items listed above in the list.
2. Please use the sheet of A4 vertically or horizontally. Please fill in each column with necessary
numbers and the column with “*” for JQA use.
3. In the cases that a part of manufacturing processes of concerned products is subcontracted to other
organization by showing specifications such as processing quality and processing conditions or
that the operations of testing and inspection regarding product quality is subcontracted, please
describe its actual conditions.
4. As for the column of “Ratio of subcontracted operations,” please write the percentage of
operations conducted by the subcontractor against the total amount of operations in the relevant
processes conducted at the factory / operation site and subcontracting site concerning JIS
certification.
Regarding testing and inspection, it is not necessary to fill out the column of ratio of
subcontracted operations.
5. As for the column of “Subcontract management,” please describe as follows;
1) In the case that a part of manufacturing processes is subcontracted to other organization:
(1) As for the column of “Control items and quality characteristics,” please describe
control items (processing conditions) and quality characteristics (processing quality) with
their specified values on the process.
(2) As for the column of “Control and inspection methods,” please describe the
control and inspection methods corresponding to control items and quality characteristics.
2) In the case that test and inspection for products are subcontracted to the other organization.
(1) As for the column of “Control items and quality characteristics,” please describe
the items of test and inspection.
(2) As for the column of “Control and inspection methods,” please describe the cycle
for requesting the test and inspection and the number of samples.
6. Please classify subcontracting process into manufacturing process, testing, manufacturing facility
and inspection facility.
7. Please delete unnecessary parts (such as “Note” here, page, etc.) in this form when preparing the
description paper.
6. Description of quality management system:
6-7 Procedures and outline of complaint handling
Customer
Inform
No
Acceptance? to
Custome
Yes r (stop)
Acceptance of customer
complaint (within 48 hrs)
No
Effective?
Yes
Review & updating relevant
Form number: (E) 8211-04J
Reporting to
documents &customer
trainings
Customer
(corrective action report)
Document describing the quality management implementation condition
[Note] 1. Please describe the flowchart for of complaint handling specified in your company standards (system
chart).
2. Please use the sheet of A4 vertically or horizontally. Please keep the column with “*” for JQA use.
3. Please attach a copy of the internal standards such as “complaint handling procedure”, “control procedure for
nonconforming product” with its prescribed form.
4. Please delete unnecessary parts (such as “Note” here, etc.) in this form when preparing the description paper
[Note] 1. Please describe the system of the company standards (rules) throughout the entire company.
2. Please make a list of company standards (specifications, rules, instructions, work standards and such)
relevant to the products to be certified among above.
3. Please attach a copy of the internal standards equivalent to a product standard (for example, specification
which specify the performance etc.) and a product testing standard (for example, testing regulation for
confirming the quality required by JIS).
4. Please describe the procedure of issue on each standards (preparer, verifier, acknowledger) and period of
review.
5. Please delete unnecessary parts (such as “Note” here, etc.) in this form when preparing the description
paper.
[Note] 1. Regarding quality records specified in the company, please describe its list and the defined period for
preservation.
2. Storage term of quality records regarding JIS Mark products is needed for at least three years.
3. Please delete unnecessary parts (such as “Note” here, etc.) in this form when preparing the description paper.
[Note] 1. Please make entry of the monthly production results (amount and unit) of the JIS pertinence
product.
1) For Initial Factory Audit, please describe the production results of six months.
2) For Periodic Surveillance, please describe the production results of the past three years (until
the month of the application for the Periodic Surveillance).
2. Please describe the outline of procedures for preparing statistical data used for the management of
concerned products (including control charts for quality management and process control).
3. Please describe the statistical data specifically prepared (similar model is acceptable).
1) For Initial Factory Audit, please describe (or attach) the statistical data of three months.
2) For Periodic Surveillance, please attach the statistical data of the latest six months in which
you manufactured the products.
4. Please delete unnecessary parts (such as “Note” here, page, etc.) in this form when preparing the
description paper.
[Note] 1. Please outline how the latest version of JIS standards regarding the concerned products is
managed.
2. Please use the sheet of A4 vertically or horizontally. Please keep the column with “*” for JQA
use.
3. Please describe the list of JIS standards specifically controlled.
4. Please delete unnecessary parts (such as “Note” here, page, etc.) in this form when preparing the
description paper.
Items Contents
(1) Name Vineet Kumar Singh
(Country language)
(2) Date of birth 18.11.1987
(3) Occupation QC Manager
(7) Acquisition of expertise on standardization and quality management (Fill in the appropriate column
out of the following items of a, b, c and d)
( )
* (For JQA use)
[Note] 1. This document is prepared in the Word format. Please adjust yours to this format, if you use other
software.
2. Please use the sheet of A4 vertically or horizontally, and please fill in each column with necessary
numbers please keep the column with “*” for JQA use.
3. As for the column (3) “Occupation,” please describe the specific name of his/her current job (to
the extent that the organization is recognized).
Machines ELECT / F - 08