Quality Inspection Quality Assurance Supplier Audit Service In China

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Quality Inspection Quality Assurance Supplier Audit Service In China Quality Assurance Service (Suzhou) provides quality inspection, supplier audit and procurement services in China.

For more info by:
WhatsAPP: 0086 159 62528467
E mail: [email protected] Quality Service|Quality Inspection|Supplier Audit in China

QAS_Your Quality Partner In China.QAS provide Quality Inspection, Quality Control, Supplier Audit and Factory Acceptance...
12/03/2022

QAS_Your Quality Partner In China.
QAS provide Quality Inspection, Quality Control, Supplier Audit and Factory Acceptance Test services for you in China.

Service needed? Please contact us:
WhatsApp: +86 159 6252 8467
Email: [email protected]
https://lnkd.in/gVGN629W

Do you Know what is CTQ? How to define CTQ? How to control CTQ?Please follow QAS_Your Quality Partner In China to get th...
06/03/2022

Do you Know what is CTQ? How to define CTQ? How to control CTQ?

Please follow QAS_Your Quality Partner In China to get the answer.

More info please contact QAS China:
WhatsApp: +86 159 6252 8467
Email: [email protected]
https://lnkd.in/gVGN629W

How to deal with abnormal quality? Follow the process!One of the responsibilities of quality personnel is to timely find...
27/02/2022

How to deal with abnormal quality? Follow the process!

One of the responsibilities of quality personnel is to timely find and feedback quality abnormal quality in production, and trace the implementation of on-site improvement measures. To track the improvement effect, to ensure that only qualified products can be transferred to the next process, to produce high-quality products.

Number 01 .
Responsibilities of quality person.

1. Familiar with the control of the scope of the process.
2. Confirmation of incoming materials.
3. Conduct inspection according to the operation instruction (First Article inspection, During production process inspection).
4. Make relevant quality records.
5. Timely find and feedback the abnormal quality situation in production, urge the implementation of improvement measures on site, and track the improvement effect.
6. Tracking and recording the quality of special products.
7. Timely remind the site of obvious identification of all materials and finished products to avoid confusion.
8. Timely correct operators' illegal operations and urge them to work according to the operation instructions.
9. Confirm the quality and identification of the products in the next process.

Number 02 .
Reasons for possible quality abnormalities.

The quality abnormality of production site mainly refers to the batch disqualification or tendency of batch disqualification of supplied materials and self-made parts found in the production process. The reasons for abnormal quality are as follows:

A. Unqualified incoming materials include unqualified incoming materials of upper process and workshop.
B. Employees do not operate in accordance with the operation instructions, and new employees work without training or without meeting the requirements.
C. Incorrect positioning of fixture.
D. The device is faulty.
E. Errors in drawings and technical documents.

Number 03 .

General handling process of quality abnormality.

1. Determine the severity of the anomaly (speaking with data)
2. Timely feedback to the quality team leader and production extension, and analyze the abnormal causes together (stop notice should be issued immediately when the defective rate is high)
3. Find out the abnormal cause and feedback to the relevant department
(1) Feed back the reasons of incoming materials to improve the process.
(2) Feedback of human operation factors to the production department for improvement.
(3) Machine reason feedback equipment Department.
(4) Process reason feedback to engineering department.
(5) Measurement error feedback measuring engineer.
4. Track the improvement effect, and if the improvement is OK, the case will be closed.

QAS Your Quality Partner In China
WhatsAPP: +86 159 6252 8467
Email: [email protected]
www.quality-assurance-service.com

Wissen Sie, wie man mit unqualifizierte Produkten umgeht?                         Die Entsorgung umfasst Folgendes: Ausw...
22/02/2022

Wissen Sie, wie man mit unqualifizierte Produkten umgeht?


Die Entsorgung umfasst Folgendes: Auswahl, Reparatur, Konzessionsannahme, Schrottbehandlung, Korrektur- und Vorbeugungsmaßnahmen.

(1) Entsorgung nicht qualifizierter erhaltener Produkte

(2) Entsorgung fehlerhafter Produkte im Prozess.

(3) Entsorgung nicht qualifizierter Endprodukte

Mehr Info, bitte kontaktieren Sie QAS China:
WhatsAPP: +86 159 6252 8467
Email: [email protected]
www.quality-assurance-service.com

Do you know what means PDCA? What are the four stages of PDCA? Follow QAS China to have a better understanding.WhatsAPP:...
20/02/2022

Do you know what means PDCA? What are the four stages of PDCA? Follow QAS China to have a better understanding.

WhatsAPP: +86 159 6252 8467
Email: [email protected]
www.quality-assurance-service.com



The four stages of PDCA

▌ The planning stage

Through market survey, user visit, etc., find out user's requirements for product quality, determine quality policy, quality objectives and quality plan, etc. Including the current situation investigation, analysis, determine the cause, make a plan.

▌ Design and implementation

Implement the contents specified in the previous phase. Conduct product design, trial-manufacture, test and personnel training prior to plan implementation according to quality standards.

▌ Inspection phase

It is mainly in the process or after the implementation of the plan, check the implementation of the situation, to see whether it conforms to the expected results of the plan.

▌ Processing stage

Mainly according to the inspection results take corresponding measures. Consolidate achievements, incorporate successful experiences into standards as far as possible, standardize and transfer the remaining problems to the next PDCA cycle to solve. The consolidation measures and the next steps.

Today's Topic:In VDA 6.3 process audit, will the question not reviewed be scored 10 points or NA?          Please visit ...
11/02/2022

Today's Topic:

In VDA 6.3 process audit, will the question not reviewed be scored 10 points or NA?

Please visit answer in LinkedIn
https://t.co/Sh4sCVX9Dy
QAS Your Quality Partner In China
WhatsApp: 86 159 6252 8467
https://t.co/Sh4sCVX9Dy

Today's Topic: In VDA 6.3 process audit, will the questions not reviewed be scored 10 points or NA? ...

How to become a qualified quality manager?                  QAS China would like to share our views about the question. ...
09/02/2022

How to become a qualified quality manager?



QAS China would like to share our views about the question.
firstly, sort out the job responsibilities of all positions in the quality department, redefine the KPI of each position. Without good process support, the KPI of the quality department cannot be achieved. Then make statistical analysis of KPI every month and carry out cause analysis and corrective measures for unachieved goals.

All the above are internal planning of the department. Under the overall framework of the company, we cooperate sincerely with other departments of the company to play a role of quality connection, transmission, bond and justice.

In the phase of APQP, our department plays a connecting function to ensure that customer requirements will not be omitted or lost in the research and development process, and implement customer functions and requirements on the characteristics of products.

In terms of quality verification, our quality department plays a fair role. Any sample shall adopt standard test and verification methods to ensure the reliability of test results and fully verify whether customer needs are met.

In terms of production process control, our quality department plays a role of connecting and judging, transforming the product standards of the technical department into quality standards that can be understood and judged by operators and inspectors, and playing a role of quality judging in incoming inspection, process inspection, completion inspection and shipment inspection to prevent all defective products from flowing out.

On the client side our quality department plays the role of investigation, feedback and supervision. When customers complain or complain, we immediately initiate emergency and temporary countermeasures; feedback the problem to the responsible department and analyze the cause together with the responsible department; formulate corrective measures, and supervise the implementation of long-term countermeasures of the responsible department.

In terms of continuous improvement, our quality department plays a leading and tracking role. In the process of internal and external quality control, many problems are constantly recurring. For these problems, we should cooperate with other departments to establish projects, analyze, improve, track and summarize.

In conclusion, as a quality manager, you should start from the problem, start from the customer, solve the problem at the product level, win the trust of the customer and the management, and then improve the process and system

Does PFMEA analysis include incoming material inspection?PFMEA scope is defined by the process flow chart, including the...
07/02/2022

Does PFMEA analysis include incoming material inspection?

PFMEA scope is defined by the process flow chart, including the purchase, manufacturing, process inspection, shipping and all the process steps. The inspection process should be as "logistics" process to analyze. In the inspection process product appearance, performance can not be damaged which are the focus of PFMEA analysis.

Q: Why is it "missed" during appearance inspection?

Answer 1: the distance between the inspector's visual inspection and the parts is too far.

Answer 2: The inspector took the wrong limit sample.

Answer 3: Checking light is less than 500Lux,

Answer 4: Appearance sample has appearance damage.

In 2 days later we will have Chinese New Year. QAS wish you Good Health and all of us emerge stronger in the Year of Tig...
29/01/2022

In 2 days later we will have Chinese New Year. QAS wish you Good Health and all of us emerge stronger in the Year of Tiger!

QAS is qualified by SGS and British Institute of Non Destructive Testing(BINDT) for your NDT requirement in China.      ...
27/01/2022

QAS is qualified by SGS and British Institute of Non Destructive Testing(BINDT) for your NDT requirement in China.



Inspection needed? then please contact us:
WhatsAPP: +86 15962528467
Email: [email protected]
or visit our web: www.quality-assurance-service.com

When we need to perform First Article Inspection? Pre Production Inspection? How to verify?For the first time in product...
25/01/2022

When we need to perform First Article Inspection? Pre Production Inspection? How to verify?

For the first time in production, the product model switching, material change, shift switch (personnel), planned and unplanned downtime...FAT/Pre Production Inspection should be prepared and performed, by statistical methods of verification, at the end of the first piece of contrast, setting methods of internal manufacturing tolerance, determine whether setup process meets series production conditions, and repeat the release process.

In IATF16949 standard 8.5.1.3 verification of Job set-ups.
Job preparation is performed at the time of the first run, material change, and job change.

Verification of job readiness is also required after planned or unplanned production shutdown are added to clause 8.5.1.4.

More info about First Article Inspection, please do not hesitate to contact us by:
WhatsAPP: +86 159 6252 8467
Email: [email protected]
or visit us by our website.

Address

Tongda
Yangpu
2151000

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