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CHAPTER ONE
1.0 INTRODUCTION
1.1BackgroundOmega Fabrication Sdn.Bhd is Malacca based tooling manufacturer. It was located in
Kawasan Perindustrian Krubong, Melaka and was established in 1998. At that time, Omega
Fabrication only has a few workers, departments and the operating business focus was also
different. In the early phase of company business development, Omega Fabrication only
focuses on fabricating parts. It only own milling and turning departments in production line,
but now Omega Fabrication has own grinding, EDM/wire cut, deburring, CNC milling and
CNC turning departments.
Omega Fabrication was operating in a very systematic way and aim to be more
worldwide in business. It was incorporated in Malaysia under the Company Act in year 1999
with a paid of capital of RM5, 000,000. The most important is Omega Fabrication committed
to business and cultures in pursuit ofQUALITY EXCELLENCE. As a result of continuous
commitment to business and quality excellence, Omega Fabrication has obtained MS ISO
9001:2000 certifications. The establishment was also to provide total customer satisfaction
by driving towards continuous improvement programmed in all areas of quality, service and
total cost of ownership to achieve an excellent standard that will exceed customers
expectations.
As a local based high precision tooling manufacturer, Omega Fabrication has specialized
in its operating business through four dimensions. It was precision tooling (trim and form),
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precision machining (carbide), injection mold parts and jig & fixtures. It fabricates a wide
range of precision tools and parts of finest quality.
Figure 1.0: Sections in operating business
1.1.2 ISO Accreditation
Figure 1.1: ISO 9001:2000
Operatingbusiness
high
precisionmachining(carbide)
precisiontooling
(trim andform)
injectionmold parts
jig andfixture
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Figure 1.2: ISO 9001:2000
ISO 9001:2000 is specifies requirements for a quality management system where
organization of company needs to demonstrate its ability to consistently provide finish products
that meet customer and applicable regulatory requirements. It also aims to enhance customer
satisfaction through the effective application of the system which including processes of
continual improvement of the system, the assurance of conformity to customer and applicable
regulatory requirements.
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1.2Organizational chart
Figure 1.3: Omega Fabrication Sdn. Bhd. organizational chart
1.3Vision and Mission1.3.0 Vision
To become a reputable leader in precise tool manufacturing-Omega Fabrication vision is to be a leader in precision manufacturing and to meet global
demands for quality products in semiconductor and all high tech industries.
To provide unlimited support and services to customers in business
-Omega Fabrication also providing support and services to customer in term of operations of
business; equipments for inspection with subcontracting companies, knowledge and advice.
To improve company through ISO 9001:2000 Quality Management System
-Omega Fabrication is continually improved in ISO 9001:2000 (QMS) in order to ensure
customer satisfactions at all times.
To improve company through Quality Improve, Cost Reduction (QICR) programmed
-QICR is a programmed own and manage by Omega Fabrication itself. It is step to maintain
customer satisfaction and loyalty.
MANAGINGDIRECTOR
MANAGEMENTREPRESENTATIVE
DOCUMENTCONTROL CLERK
BUSINESSDEVELOPMENT
MANAGER
MARKETINGEXECUTIVE
ASSEMBLYTEAMS
SALES/SERVICEMANAGER
PRODUCTIONMANAGER
TURNINGSUPERVISOR
MILLINGSUPERVISOR
WIRE CUT/EDMSUPERVISOR
GRINDINGSUPERVISOR
DEBURRINGLEADER
CNC MILLINGSUPERVISOR
CNC TURNINGSUPERVISOR
QUALITYASSURANCEEXECUTIVE
PLANNINGEXECUTIVE
STORE ANDDELIVERY
COORDINATOR
QUALITYASSURANCESUPERVISOR
FINANCE ANDACCOUNTOFFICERS
DESPATCHASSISTANT
PURCHASINGOFFICER
HUMANRESOURCE
OFFICER
GENERALMANAGER
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1.3.1 Mission
Omega Fabrication Sdn.Bhd. mission is to continuously grow and improve in partnership
with customers to provide quality, delivery, competitive price, service and support and
customer satisfaction at all times.
Omega Fabrication Sdn.Bhd always focuses to identify customer need through continual
technological improvement and open continual communication. They always put on
believes with customer-supplier relationship and continually striving for improvement in
quality. Therefore, they always at high expectation to provide customer with cost
effective, on time delivery with excellent service and support.
1.4Quality Policy
Figure 1.4: Omega Fabrication Sdn. Bhd. quality policy
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1.5Competitive advantageI have defined Omega Fabrication Sdn. Bhd. competitive advantage into four sections. The
competitive advantages are quality, machinery, capacity and competency.
(A)QualityOmega Fabrication Sdn. Bhd. always aims and provides customer with the highest
and finest quality products as it is the local based high precision tooling manufacturer.
It fabricates a wide range of precision tools and parts of finest quality. As a proved
Omega Fabrication Sdn. Bhd. has customer from a widen industrial sectors such as
semiconductor sector, energy or oil and gas sector, aerospace sector, industrial
automation sector, shipping sector and precision engineering sector.
(B)MachineryOmega Fabrication Sdn. Bhd. always focuses to identify customer need through
continual technological improvement and open continual communication. Therefore,
the machinery provide in the production line in every departments such as milling,
turning, deburring, EDM/wire cut, grinding, CNC milling and CNC turning
departments are all high technology machineries. Further, the machineries provide in
quality assurance departments are also high technology machineries. It is to support
Omega Fabrication Sdn. Bhd. motto, Quality is our priority.
(C)CapacityAccording to Omega Fabrication Sdn.Bhd. mission, continuously grow and improve
in partnership with customers to provide quality, delivery, competitive price, service
and support and customer satisfaction at all times. Therefore, I found that every day
store and delivery coordinator and quality assurance supervisor set and manage the
outgoing of finished products to deliver to customer. Then, planning executive and
quality assurance executive also paid their responsibility to make sure and maintain
the capacity of outgoing finished products should be done every day is achieved. This
is because Omega Fabrication Sdn. Bhd. always served customers with delivery on
time.
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(D)CompetencyOmega Fabrication Sdn. Bhd. also has many technical expertises which are very
competence to their quality of work. Even though, some of the operators are hired
from Myanmar, Indonesia and Nepal, but they are very competence to their work too.
This is because all of them are really understand and focuses to company visions and
missions.
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1.6Business process flowCUSTOMER
BUSINESS
DEVELOPMENT
PLANNING
PURCHASING/STORE
PRODUCTION
SUBCON
QUALITY
ASSURANCE
CHECK
ACT
Figure 1.5: Business process flow
Customer
enquiry
Customer
receive
quotation
Deliver to
customer
Customer
issue
Purchase
order (PO)
Prepare
quotation
Review order
Resources Resources
planning
Order
materials/parts
Check stock Store Prepare
invoice
Production
Heat
treatment/finishing
treatment
QA in process
check
QA incoming
control
QA final
inspection
Packing
Internal audit
Management review
Continuous
improvement
YES
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CHAPTER TWO
2.0 THE INDUSTRIAL TRAINING PROGRAMME
2.1 Scopes of responsibility
During my training session in Omega Fabrication Sdn Bhd, I have been located in
Quality Assurance (QA) department which comprises with quality control team. Along this
experience my major job scopes was to generate quality assurance finish product inspection
report and key in data of the outgoing products in the system.
Here, I have found that quality is not the responsibility of any person or only for QA
department, but it is everyones job. From the theory in Quality Management subject, I learnt
that areas responsible for quality control are marketing, design engineering, procurement,
production, process design, inspection and test, packaging and storage and customer. Therefore,
from the issues rise in QA department which will be discussed in Chapter 4, I concluded that
quality of finish products was not only the roles of QA department but also every department
should play their roles to maintain and make sure the finish products were in good quality.
I have seen that quality assurance does have the direct responsibility to continually
evaluate the effectiveness of the quality system and it also determines the effectiveness of the
system, appraises the current quality, determines the quality problem areas or potential areas and
assists in the correction or minimization of these problem areas. In my opinion, the overall
objective of QA department was the improvement of the quality in cooperation with the
responsible departments. Below is QA finish product inspection report form.
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Figure 2.0: Diagram of Quality Assurance finish product inspection report form
The most important I have learnt in written the QA finish product inspection report form
was about dimensions, sampling size, instruments used, tolerances and treatment processes. For
dimensions, I should be able to recognize whether the dimensions were controlled or non-
nstruments used
Dimensions
Sampling sizeTreatmentProcesses
Tolerances
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controlled and learnt many symbols of dimensions in the technical drawings. For sampling size, I
had to determine the sampling size with the given quantity of finish products. It just like what I
have learnt in Business Statistics subject. Below is the sampling plan that I was dealing with
every day.
Figure 2.1: The sampling plan of QA finish product inspection report
The purpose of sampling size was to determine the number of finish products need to be
inspected if finish products were too many. For tolerances, I had to calculate and make sure the
actual measurement of finish products from the inspection were in specs. If the actual
measurements were out of specs, I needed to remind and alert to the quality control inspector.
Others, for controlled dimensions, I needed to use Information Tolerances Tables to calculate
and make sure the actual measurement from the quality control inspector was in specs. The
Information Tolerances Tables were including with x-axis and y-axis. The x-axis was the ISO-
symbol and the y-axis was the nominal. The most important I have learnt from it was the
calculation of dimensions based on the technical drawings.
For treatment processes I had opportunity to learnt a lot about finishing, harden andmaterial. Here, I had viewed and got a lot of information of finish products which undergone for
types of finishing and harden processes from different materials. Below are finish products that
undergone for treatment processes; white zinc and electroless nickel.
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Figure 2.2: finishing; white zinc
Figure 2.3: finishing; electroless nickel
Finally for instruments used, I learnt about the correct checking method for finish
products which comply with requirement. It really complied with my Manufacturing Process
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subject. First, I learnt how to measure the dimensions of diameter which complied with
requirement. For controlled hole diameter, 0.5mm to 20.01mm was needed to use pin gauge,
20.01mm to 50.01mm was needed to use bore gauge, 50.01mm was needed to use smart scope,
coordinate measuring machine (CMM) and 0.4mm was needed to use smart scope. For outer
controlled diameter, 0.001mm-150.00 mm was needed to use micrometer (clamping test) and
150.01mm was needed to use CMM. For non-controlled diameter was needed to use caliper. For
dimension, internal controlled distance 0.005mm to 200.00mm (slot) was needed to use block
gauge and distance from 0.005mm to 600.00mm was needed to use height gauge or CMM. For
dimension, external controlled distance was needed to use smart scope, height gauge and CMM.
For non-controlled dimension was needed to use caliper. For flatness or parallelism was needed
to use dial test indicator. For checking screw was needed to use fitting test according to the size
and depth. For normal thread or special thread was needed to use thread gauge and fitting test
according to the thread. For angle and radius was needed to use protector, smart scope and
CMM. For treatment the confirmation must certified with certificate of compliance.
I was also dealing with the certificate of compliance for customers which were the
certificate of compliance from finishing process, certificate of compliance of hardened process
and material certificates. Normally, every week I was needed to recognize, separates and filing
the hardened, finishing and material technical drawings completed with its inspection report to
scan and key in the outgoing finish products data according to customer purchase order number
and date. The requirements needed to send the inspection report and certificate of compliance to
customer was only for two days. Therefore, it was my responsibility to keep in touch and deal to
customer with the inspection report and certificate of compliance. The inspection report was very
important as it was customer requirements where it would be as a reference for both if any
troubles raised to the inspected finish products after it had been delivered to customer.
Meanwhile, the certificate of compliance function was as a proved to customer that the finish
products had undergone treatment processes; finishing, hardened and material.
My minor job scope was checking simple finish products. I was not be able to check
complicated finish products due to time frame obstacle which there was a lot of urgency finish
products need to be inspected every day. But the QA team always gave me added information
especially in inspected the complicated finish products. It was especially the symbols and metrics
which include the first, second and third view of the technical drawings. This was really added
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information for me because I have not learnt Technical Drawing subject before but I was very
interested at it as I was dealing with it along this six months of training sessions.
Furthermore, I learnt about the instruments used in checking finish products and its
correct checking method. This was applied with the theories I learnt in Manufacturing System
subject which included the instruments used in checking the finish products. The instruments
available in QA department were analog vernier, dial indicator, digital vernier, smart scope, pin
gauge, micro meter, dial caliper, block gauge, height gauge, fitting test, CMM and bore gauge.
Below are the pictures of equipments for inspecting finish products.
Figure 2.4: digital vernier caliper
Figure 2.5: bore gauge
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Figure 2.6: micro meter
Figure 2.7: block gauge
Figure 2.8: fitting test
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Figure 2.9: smart scope
Figure 2.10: coordinate measuring machine
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Figure 2.11: height gauge
Finally, regarding to my job scopes which key in data in systems. My routine was also
key in data and recorded the number of outgoing products. The system used for this job scopes
was Automated Business System. It complied with my Management Information System subject
whom nowadays many companies used significant systems to easily manage and operate its
businesses. This was very important because by key in the outgoing finish products data the store
and delivery coordinator and the planner of company were easily coordinate and target monthly
sales performance. The data were comprises with customer purchase order number, technical
drawing part number, delivery date, types of materials, weights and quantity.
2.2 Important and significant of my responsibility to the organization.
Regarding to my job scope generating QA finish product inspection report was very
important as it was customer requirements when delivering along with the inspected products.
This was because when something defected was determined, so customer would refer to the
inspection report. Therefore, my job scope was very important as I was also responsible to
maintain companys status. Finally, the inspection reports were also needed for achieving
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CHAPTER 3
3.0 INDUSTRIAL TRAINING ASSIGNMENTS
My industrial training assignments at Omega Fabrication Sdn. Bhd. Quality Assurance
Department are to generate quality assurance finish product inspection report, key in data in
computer and dealing with certificate of compliance and inspections reports for customer.
For the first task is generating quality assurance finish product inspection report. I would
like to enlighten that generating quality assurance finish product inspection report is not an easy
task. The strongest reason is because this inspection report would be as reference for customer if
any problems occur with finished products. The problems usually occur such as dimension
problems which comprises with the controlled and non-controlled dimensions, finishing and
harden problems and materials. In my opinions, generating quality assurance finish products
inspection reports is a big responsibility as I am also bring the company s name and status to
customer. In Omega Fabrication Sdn.Bhd. also have a very worldwide customer which they are
from Europe, South East Asia, Japan, Dubai Emirates and Malaysia. Therefore, I am also
involving myself with the worldwide customer.
According to ISO 9001:2000 Requirements Mandatory Procedure, it comprises the
elements; control of documents, control of records, internal audits, control of non conformity
products, corrective and preventive actions. Regarding to my daily task, the quality assurance
finish product inspection reports are also called as control of documents for auditing with
International Organization for Standardization. Usually the audit session will be held once in the
ends of the year. Before I explain more on my task, generating quality assurance finish product
inspection reports, I would like to explain about the operational quality control checking flow.
Operational quality control checking flow is guidance for quality control inspectors in doing
their responsibility to check the finish products. Below is the operational quality control
checking flow that quality control inspectors used in Quality Assurance department.
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Figure 3.0: Operational Quality Control checking flow
In operational quality control checking flow, first, QA department received part for
inspection session from production department. Usually, before the Head of Department dividingpart received to quality control inspectors for checking, I would update the daily output products.
Daily output products means the total number of parts need to be checked and had been checked
in QA department. After completed updating the daily output products, the Head of Department
was dividing the parts to quality control inspectors. Second, once parts received to quality
control inspectors, they need to check the quantity of the parts as required in the technical
drawings. Third, they need to check the material used is as indicated in the technical drawings.
Fourth, they need to check the finishing parts such as surface finishing; electroless nickel, clear
anodize, hard chrome, flash chrome and chemical passivation and harden; HRC 58~60 and
709/760 nitri hard. Fifth, they need to study the dimensions in the technical drawings and
recognized the controlled and non-controlled dimensions. Here, they need to use the correct
equipment as indicate in the checking method.
1. PART RECEIVED
2.CHECK QUANTITY
3. CHECK MATERIAL
4. FINISHING
5. DIMENSION
6. INSPECTION REPORT
7. APPROVAL
8. PACKING
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Sixth, is the part whereby it is my responsibility to generate the quality assurance finish
product inspections reports. I need to transfer the entire inspected dimension to the inspection
reports and I must to make sure that all the dimensions is in specifications as required in the
technical drawings. In my opinion, generating the quality assurance finish products inspection
reports is an added value for me as I am learning a lot in the equipment used for the right
checking methods, symbols in the technical drawings and I am able to know and use the ISO
tolerances effectively and efficiently. This is really a very valuable knowledge for me. Seventh,
after the inspection report is completed, final approval of inspection from the Quality Manager is
need before all the parts send for packing. Finally, was the packing session.
My responsibility is not just generating the inspection reports, but I must alert with the
requirements in the technical drawings and customer. The requirements are such as the materials
certificate, certificate of compliance of hardening and treatment processes. This certificate is
send as a proved for customer. Others, generating the inspections reports also create me to be a
responsible person by whom I need to aware the quality control inspectors if the inspected
dimensions were not in the range of specifications. In my opinions, generating the inspections
reports was the risky tasks for me. This because I am also will be the important person if any
problem occurs to the parts send to customer.
According to Besterfield (2008) has state that Quality Function Deployment is a system
that identifies and sets the priorities for products, services and process improvement
opportunities that lead to increased customer satisfaction. Regarding to my task I am also
involving myself in completing the non-conformity report from customer. After the quality
control inspectors had discussions among them about the problem assigned in the non-
conformity report, then, the head of department will explained and discussed to me how to
complete the non-conformity report. Usually, I am key in data of the corrective actions for non-
conformity report and send it to customer e-mail. In my opinion, the quality function deployment
process creates good relationships for both customer and supplier and it leads to increased
customer satisfaction. This is because quality function deployment ensures the accurate
deployment of the voice of customer throughout the product planning to field of service.
According to my opinion, in serving the best quality for customer, not only one department
responsible to give the best quality of work but all the entire departments in company should
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paid their good responsibility to provide goods and services that meet or exceed customer
demands.
Below is the operational quality control flow chart. This flow chart shows clearly which
parts should be delivered to customer and keep in store.
Figure 3.1: Operational Quality Control flow chart
PART RECEIVED IN
OQC
SEGREGATION
REWORK/REMAKE
NEW
COMPLETE PROCESS
GREENSTICKER
CHECKING
PACKING
ISSUE QA REJECT
REPORT
CUSTOMER
QC REPORT LABEL
CUSTOMER P.O
STORE
UPDATE STOCK AND
STICKER
INCOMPLETE
PROCESS ORANGE
STOCK
QC REPORT
VERIFICATION
NO
YES
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assurance, improve my communication skills and also give me wide experience about
equipments used in quality control.
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CHAPTER 4
4.0 INNOVATIVE SUGGESTIONS
Regarding to my job scopes is to generate quality assurance finish products inspection report and
handling certificate of compliance and inspection report for customer, here I come out with
several suggestions. My purpose to come out with these innovative suggestions is to give ideas
for my Quality Assurance department and also the entire company in order to have a better
quality management system.
Problem 1: Problem in filing documents for ISO
The International Organization for Standardization has developed ISO 9001:2000 as a
means for company to institute quality management systems through a set of controlled
procedures and practices. ISO 9001:2000 also specifies requirements for a quality management
system where an organization needs to demonstrate its ability to consistently provide product
that meets customer and applicable regulatory requirements and aims to enhance customer
satisfaction through the effective application of the system including processes for continual
improvement of the system and the assurance of conformity to customer and applicable
regulatory requirements. The purpose of ISO 9001:2000 standards is to promote the habit of
evaluating operational processes and it fundamental principle resides in working through process
improvement to achieve product quality. Omega Fabrication Sdn. Bhd. also has accredited and
certified with the requirements of ISO 9001:2000. Therefore , according to ISO 9001:2000
Requirements Mandatory Procedure, which comprises the elements; control of documents,
control of records, internal audits, control of non conformity products, corrective and preventive
actions, Omega Fabrication Sdn. Bhd. had done well all these elements to meet the ISO
9001:2000 requirements mandatory procedure.
But along the training session, I have viewed that the employees does not have anyproper way for filing all the technical drawings and quality assurance finish products inspection
report. Currently, they used a traditional way to keep and store all the technical drawings and
inspection reports. These technical drawings and inspection reports need to be kept and stored
safely as well as for an external audit. External audit is comprised of a Second Party Audit and a
Third Party Audit. The Second Party Audit is normally performed by customer such as the
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supplier and the Third Party Audit is performed by registrar such as independent audit. The main
purpose of the auditor is to validate the documentation and make sure the employees are properly
trained to do their jobs. Therefore, in my opinion by practically used this traditional way to keep
and store all the important documents for external auditing session soon, it might be raised some
problems for company. Why I say so is because I have viewed all the technical drawings with
inspection reports are kept in a store room within plastics bags and paper boxes. Besides, there is
also bulky of technical drawings with inspection reports that have not been filing on the floor in
the store room.
In my opinion, the traditional way of filing these documents is really not in a systematic
way whereby in these modern era, effective organizations should choose a very systematic way
in managing all the entire things in the company. Here, I am come out the innovative suggestions
not to complain the way of Omega Fabrication Sdn. Bhd. filing and preparing for external audit
session but I am here to give my ideas just to make the way of filing of all documents is in
effective way and can be accessible easily. There are several reasons why I say the current way
of filing is not effective. First, I imagined 10 years later, the store room will full with bulky of
documents. Second, the way to kept all the documents just in the paper boxes in the store room
really exposed to danger which is if disasters happened such as flood, fire or else the documents
are exposed to pests such as termites, so, there is no secure back-up and the documents will
damaged beyond repair. Third, it is a long time consuming when need to retrieve the documents
in emergency cases. Fourth, the documents now would not be accessible and untraceability and
finally, this traditional way of filing are unsecure because documents can be easily lost.
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Solution for Problem 1: Document Management System
Figure 4.0: Components of Document Management System
According to this cases, I suggest that Omega Fabrication Sdn. Bhd to implement a
Document Management System for filing. Document Management System is any software that is
used to provide an efficient manner of collecting documents, storing them and making retrievaleasy. The benefits of implementing this system are many. First, it improves employee
efficiencies by eliminating the manual processes and also leading to improved information,
increased productivity and better process consistency. Second, it promotes flexible documents
retrieval which is less time is spent for locating the documents as they can be retrieved the
documents without leaving the desk. Other, Document Management System also very flexible as
the users can also access other systems as retrieving the documents. Compared to the traditional
way employees need to spent much time for finding the documents from the storage especially in
emergency cases and it becomes the situation more worst. Third, no more lost documents which
are losing technical drawings and inspection reports usually make trouble for my quality
assurance department team as they need to deal and serve customer on time in order to gain
customer loyalty. Fourth, it will be as disaster recovery strategy. In my opinion paper is a bulky
and expensive way to back-up records and also is vulnerable to fire, flood, vandalism, theft and
RETRIEVAL
STORAGE
LOCATINGAUDITING
INDEXING
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finally it will improved security as it can provide better, more flexible control over sensitive
documents.
What are Document Management System requirements?
According to MacKechnie (2003) state that Document Management System are changing the
way of organizations store and retrieve documents and replaced the old-school files and cabinets
with new and high technology tools. By referring to Omega Fabrication Sdn. Bhd. traditional
way in filing the technical drawings and inspection report, usually the employee took a very long
time for arranging all the technical drawings. One of the way in arranging the technical drawings
and inspection report are by following the job number of the drawings manually.
Therefore, the requirements of Document Management System are scanner, document
management software and storage device. First, the scanner will be function as to scan all the
technical drawings and inspection report that completely undergoes inspection session. Second,
document management software that drives the Document Management System. Document
Management System is only as good as the software that drives it. Third, storage device which is
range in size and functionality.
How the Document Management System works for filing?
Figure 4.1: Sample workflow of filing
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Once the technical drawings are completing with the inspection reports, first it will be
send to customer as requirements from them. Then, the technical drawings and inspection reports
are scanned to run in the data in Document Management software for filing. The documents will
be run in the classification system which are refer to the customers name, job number or
purchase order number. After that, data will be circulate in the system which the technical
drawings and its inspection reports are available for certain departments in Omega Fabrication
Sdn. Bhd. such as Quality Assurance Department and Store & Delivery Finished Goods
Department. Therefore, if any problem occurs such as non-conformity reports raised from
customer after delivery the finished products, so the problem will solve immediately in action
whereby the documents can be retrives as soon as posible by using Document Management
System. Compare to the current way of filing the technical drawings and its inspection reports,
usually the employees take longer time to retrieve the documents. The effieciency of productivity
also can be improved as customer satisfied with the services company has served. Others, by
using this system staffs in department can simply forward the documents among the team
department as they did not need to move around for discussion the problems and the percentage
of lossing the technical drawing and its inspection report also decreased. In conclusion, everyone
can paid their efficiency and effective way of working environment as the system are enabling
instatnt access to documents.
For external auditing session, by implementing Document Management System, the way
of filing all the technical drawings and its inspection reports will look more systematically and
organized.
Figure 4.3: Current way of filing Document Management System
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Problem 2: Internal design in Quality Assurance Department
In my opinion the internal design for Quality Assurance department is not too comfortable for
quality assurance team working environment. The reason is because all the equipments for
inspecting the products are kept in one room with the entire workers table. Below is the sketch of
my Quality Assurance department.
Figure 4.4: Sketch of Quality Assurance department room
Solution for Problem 2: Separate the room of equipments
My suggestion is Omega Fabrication Sdn. Bhd. need to separate the room of equipments or
inspection parts and the room of workers. My strong reason is normally sometimes the lossing of
finished products and its technical drawings is because the room of quality assurance department
is full of urgent products that need to be inspected. From my experienced along this training
session, the situations in my quality assurance department becomes more trouble when there is
Workers table
Height gauge
CMMSmart scopeRack of files
Others
equipments,
computers,printer
Workers racksFinish products signature
part
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many urgent products located in department and each of the products need to inspect carefully.
In my opinion, eventhough it is much costly to change the internal design, but for a long term
vision its quite gives more benefit to company profitability and productivity. Moreover, I think
with this innovative suggestion, the situation for inspecting the finished products will be more
organized, strategically and the number of non-conformity reports can be reduced.
Problem 3: Increasing of non-conformity reports (NCR)
Non-conformity reports are reports which issued when finish products, processes or procedure
does not comply with the set standards for particular belongings to the finish products, processes
or procedures under inspections. According to Besterfield (2008) has state a Cause and Effect
diagram is a picture composed of lines and symbols designed to represent a meaningful
relationship between an effect and it causes. Therefore, I have defined the increasing of non-
conformity reports by using Cause and Effect diagram advocated by (Ishikawa,1982 ).
Figure 4.5: Cause and Effect diagram of increasing of NCR
INCREASING
OF NCR
MATERIAL METHOD
MACHINERY ENVIRONMENT MEASUREMENT
MANPOWER
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Solution to Problem 3: Materials, environment, method, manpower, measurement and machinery
There are six causes that caused the increasing of NCR. For materials, sometimes the materials
used in producing the requested products from customer would not be able to be inspecting from
quality assurance team. This is because the materials properties are much sensitive and are not be
able to be inspecting with the equipments. It might be because the planner and production lines
want to follow and meet customer requirements but they were less thinking about the ability of
quality assurance team during inspecting the products. According to this situation, I suggest that
before accepting customer order, the planner should study the technical drawing and
requirements from customer first and understand carefully whether all departments have their
ability to run out the products as they can pay 100% responsibility to increase the company
profit.
For environment, I found that the temperature in my department is cold. It is about 21
degree Celsius. The reasons are to keep the CMM machine, height gauge and smart scope in
good condition. All these expensive equipments need to be in cold condition. Therefore, these
cold temperature will cause some of materials of finish products been shrink and it will cause my
team to get inaccurate measurement result during inspection session. According to the situation
had happened, which customers have complain that they have different measurement of
inspection result compare to my team measurement of inspection result. This is because the room
temperature where finish products been stored also influenced the measurement of inspection
results. According to this situation, I suggest all the finish products that come from the
production department must be stored in one room which the room temperature is in normal
room temperature. Meanwhile, all the equipments use in quality assurance department must be
placed in one room which these equipments need to stay in cold room temperature.
For method, I found that error easily occur everywhere. First, from the inspection
sessions my team detected missing process by production department. Second, error occursduring the inspection time such the inspector forgets to inspect some dimension which is control
or non-control. Third, error occur during writing the quality assurance finish product inspection
report as there are many dimensions of complicated technical drawings need to be written.
Fourth, my company got complains from customer as we deliver more or less finish products
differ from the customer purchasing order record. All these occur because of human limitations
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as they need to inspect many products in a day and feel of tiredness. According to this situation, I
suggest that everyone in this company should always practice and follow the quality
management vocabulary which is doing it rights at first time and always be responsible with
the tasks they need to complete.
For manpower, in my opinion, the number of workers in my quality assurance
department is not enough to handle all the urgent products that need to be inspecting in a day.
Due to situations that I also faced during writing the quality assurance finish products inspection
report, I need to do many of inspection reports in a day. So, time planning and time management
is very important every day. Every day I found my quality assurance team will be rushed to
complete inspecting all the urgent products and usually they need to do overtime working hours.
Therefore, the workloads for them in a day are high and it will decrease their focus on
completing all the tasks given. According to this situation, I suggest my company to hire new
workers with high skill and experiences in using the equipments in quality assurance department
or another solution is to do shift working hours rather than practice normal shift working hours
as usual now.
For measurement, in my opinions some of my quality assurance team is lack of training
in inspecting the complicated finish products. This is due to situation happened which not all my
quality assurance team is able to inspect the complicated finish products. Complicated finish
products mean finish products which have a lot of dimensions, big sizes and complicated shapes.
Some of them are also lack of skill to use the equipments such as CMM machine. So, other team
members need to help the one who lack of skill in inspecting the finish products. This will cause
trouble and lack of focus of other team members in inspecting their finish products as there are
many urgent finish products need to be handled every day. The most important that I want to
enlighten here is about technology readiness which I have found that some of quality assurance
team members are not well-adapted with the high technology equipments. According to this
situation, I suggest that my quality assurance team members should attend several courses of
training which would make them very adaptable with all the high technology equipments provide
in quality assurance department.
Finally, for machinery in my quality assurance department are all high technology
equipments. Usually high technology equipments are very costly. Based on what I have learnt
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before in Microeconomics subject, usually organization need to minimize cost and maximize
profits. Therefore, in this situation I understood why there are only few high technology
equipments provide in my quality assurance department but in my opinion I have seen these few
high technology equipments as a problem in handling all the urgent finish products every day. I
think my quality assurance department is lacking of inspection equipments. The reasons are
because my quality assurance team members usually need to queue among them in inspecting the
finish products. The situation becomes very trouble if there are many urgent products which need
to be inspecting by using the same equipments.
Therefore, once my quality assurance department received non-conformity report from
customer, the first solution that usually they do are discussing among them whether they should
take preventives or correctives actions regarding to the problems stated in the non-conformity
reports. The ways to solve the non conformity reports can be variously as it depends on the
problems occur. Once they have decided the solutions, they will let customer know the cause of
problems occur and also let them know whether to take correctives or preventives actions.
From this issue, I observed the non-conformity report really related to the ISO 9001:2000
requirements mandatory procedure. The requirements mandatory procedure are;-
(A)Control of documentsControl of documents is the finish products inspection reports that usually my department
releases with the outgoing of finish products after it completing the final inspection.
(B)Control of recordsControl of records is recorded data of outgoing finish products by using the Automated Business
System and the recorded data of rejected parts after it releases from production department and
undergoes the inspection sessions.
(C)Internal auditsUsually the internal audits will occur once a year. This to enhance the finish products always
meet customer satisfactions and company business operations is following the ISO 9001:2000
certifications.
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(D)Control of non-conformity productsControl of non-conformity products is measurement of organization to handle the non-
conformity products such as training in using the high technology equipments in inspection.
(E)Corrective actionAction takes when problems occur.
(F)Preventive actionAction should be aware from repeating the same problems.
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CHAPTER 5
5.0 CONCLUSION
In conclusion, this industrial training gave me a lot of experienced and precious of
knowledge. Along these six months in Quality Assurance department I have gained a lot of
information and knowledge which much related with my Bachelor Degree in Technology
Management and Innovation. I also have gained much add-up knowledge such as learning a lot
in technical drawing especially the symbols and the equipments used in inspecting the products.
The working environment also teaches me a lot that time management and strategic planning is
very important in paying our responsibility to company. Others, this industrial training gave me
opportunity to explore more on the theories that I have learnt in Bachelor Degree in Technology
Management and Innovation. I am really appreciating this experience which I am able to know
the reality lives of working in an industry. In my opinion, working in an industry really
challenges me and my abilities to adapt with working environment which sometimes it become
so much stressed but in the end I know this is really a precious moments. I am also learnt to be a
more responsible person as I am doing my job scopes and able to come out with my innovative
suggestions. These experiences really make me feel theories are easy to be learnt but it is
difficult to implement if there is no discipline and responsibility in everyones selves.
5.1 Bachelor Degree Dissertation
For Bachelor Degree Dissertation I would choose a topic on clean technologies innovation and
introduction. I am very interested at this topic because I am really eager in learning technology
innovation subject and it is my hobby to explore and knowing on the latest technology.
Moreover, nowadays I see pollutions problems occurred everywhere. There are many
types of pollution occurred such as air pollution, water pollution and sound pollution. As we
know these pollutions would disturbed and harmed human lives and activities. Regarding toclean technologies, I am interesting in exploring and researching in preventing the air pollutions.
At this time, I got the idea either in upgrading the current clean technologies or else in
introducing the new technologies in preventing the air pollutions. In this modern era, we have
many air cleaning technologies such as industrial vacuum systems, industrial dust collectors,
asphalt smoke control, portable air cleaners, woodworking dust collection and restaurants
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exhaust. Therefore, by exploring more on this topic I hope I can upgrade or introducing a new air
cleaning technologies.
My objectives to choose on clean technologies innovation and introduction are first, I
would like to challenge myself in exploring and researching the new air clean technologies.
Second, I would like to provide the minimal level of air pollutants and third, I would like support
The Ministry of Science, Technology and Innovation, Malaysia objectives to enhance the
capability of technopreneurs to increase industrial competitiveness through technology transfer.
Thus, I would choose Dr. Chew Boon Cheong from Faculty of Technology Management and
Technopreneurship as my supervisor for Bachelor Degree Dissertation.
The most important thing that I can relate with my experienced along the industrial
training in Quality Assurance department is quality is not just responsibility of any one person,
but it is everyones job. It is same as the topic of clean technologies innovation and introduction
which we as people in this world must paid our responsibility to the world to create and innovate
the cleaning technologies to maintain good quality of lives.
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REFERENCES
1. Russel, R.S. and Taylor, B.W., 2011. Operations management. 7th ed. United Statesof America: John Wiley and Sons, Inc.
2. Robbins, S.P. and Coulter, M., 2009. Management. 10th ed. New Jersey: PearsonEducation, Inc.
3. Besterfield, D.H., 2008. Quality Control. 8th ed. United States of America: PearsonEducation, Inc.
4. Laudon, K.C. and Laudon, J.P, 2012. Management Information Systems. 12th globaled. United Kingdom: Pearson Education, Inc.
5.