Understanding The ISO/TS
16949:2002 Standard
5.5.2 Management Representative
Top management
must:
Appoint a member of management as the Management Representative
(MR)
Irrespective of other responsibilities, the MR shall have the
responsibility and authority to:
a)
ensure processes needed for the QMS are established,
implemented, and maintained
b)
report to top management on QMS performance and any need for
improvement to it
c)
ensure the promotion of awareness of customer requirements
throughout the organization
(Note: The MR’s
responsibilities may include liaison with external parties on
matters relating to the QMS)
5.5.2.1
Customer Representative –
top management shall designate personnel with responsibility
& authority to ensure that customer quality requirements
are addressed. This includes –
Þ
special characteristics;
Þ
setting quality objectives and related training;
Þ
corrective and preventive action
Þ
product design and
development.
Key Explanation Points and Tips:
Þ
The rationale for appointing a member of
management as the MR is so the individual has
sufficient authority to effectively carry out QMS
responsibilities. The individual should preferably be a member
of top management, but not necessarily so. The MR’s role is to
facilitate, motivate and promote the deployment of QMS
requirements throughout the organization, through guidance,
training, teamwork and assistance.
Þ
In carrying out
QMS responsibilities, the MR may need to communicate, delegate,
empower, report, oversee and interact with individuals at all
levels internal and external.
Þ
“Irrespective of other
responsibilities
” means that the MR may wear other
hats and the MR hat does not have to be the primary one.
Regardless, once appointed as the MR, the individual must
effectively perform all QMS responsibilities specified in this
sub-clause. Much
of this can be done through having access to appropriate
resources and through delegation. The MR may be a full-time or
sub-contracted person.
Þ
Top management may show evidence of the appointment of the MR
through an appointment posting; attendance at QMS review
meetings; provision of support, authorization and resources to
QMS activities.
Þ
Since quality is the responsibility of the entire organization,
the role of the MR is to assist process owners in developing
their processes according to the requirements of clause 4.1 and
applying the requirements of other specific clauses of ISO 9001
relevant to their process. For example the purchasing,
production or warehousing processes must also know how to
control nonconforming product (clause 8.3); take corrective
action (clause 8.5.2) or control their records (clause 4.2.4);
etc.
Þ
Reporting to top management on QMS
performance
may take place at management review meetings or other meetings.
The information for the report will come from the results of
the measurement and monitoring requirements specified in clause
8 (e.g. internal audits and customer satisfaction feedback,
etc.). The MR must delegate and facilitate the compilation of
this information from all the process owners.
Þ
The report must include any recommendation to improve the QMS based on
the MR’s review of all QMS measurement and monitoring data. It
would be appropriate to discuss and obtain agreement with
affected process owners.
Þ
As we discussed earlier, TS 16949 focuses heavily on
meeting customer and regulatory
requirements and enhancing customer satisfaction.
The MR must likewise promote this focus through all processes
that are directly and even indirectly involved in achieving
this. There are many ways of doing this including the use of
training; cross-functional teams; customer focused project
teams; project milestone reviews; designated customer
representative; electronic interfaces with the customer; use of
PPAP, FMEA’s, Control Plans, customer specifications, customer
product specific work instructions, etc.
Þ
The appointment of the MR and defining his/her responsibilities
ands authority should be part of the business planning process.
The MR’s activities must be included in quality planning;
management review and communication processes.
Þ
The designated customer
representative(s) and their specific
responsibilities must be clearly defined. They must ensure that
customer requirements are fully understood and addressed. A
good way to address this, is for the customer representative to
participate in the entire APQP (Advanced Product Quality
Planning) process (see reference manual).
Review specific requirements for the customer representative at
OEM customer or IATF websites.
Þ
The effective fulfillment of the customer representative’s
responsibilities may be demonstrated by their participation in
milestone and decision points related to production release;
engineering release and other related activities linked to
customer requirements.
Þ
Overall QMS performance indicators may be used to determine how
well the MR has performed the responsibilities defined in
clause 5.5.2.
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