Rise of the Machines: AI in Manufacturing and how it’s reshaping the industry
Manufacturing is undergoing a seismic shift. No longer are factories solely reliant on human labor and traditional methods. AI is rapidly transforming the industry, ushering in an era of “smart manufacturing” defined by efficiency, precision, and data-driven decision making. This revolution is fueled by the vast amount of data generated in manufacturing. From sensor readings[…]
How Kiuey’s PPAP manager empowers your PPAP/APQP processes
In today’s globalized supply chain, streamlining the Production Part Approval Process (PPAP) is crucial for both manufacturers and suppliers. Online PPAP management tools must offer a significant advantage by automating tasks, improving communication, and ensuring compliance. But not all tools are created equal, and there’s where we portrait that our PPAP Management tool is different.[…]
Dangers of Stagnation: Why Rejecting New Technology is Harmful for SQEs
The frustration crackled in Sarah’s voice as she slammed her laptop shut. “This new system is a nightmare,” she grumbled to her colleague, David. Sarah, a seasoned Supplier Quality Engineer (SQE), had spent the morning wrestling with a recently implemented quality management platform. Does that short story sounds familiar to you? The relentless march of[…]
Planning and Prioritization over Time Management: The Path to Surpass SQEs’ Time Havoc
Imagine this: John, a Supplier Quality Engineer (SQE), rushes into a meeting ten minutes late, frazzled and flustered. He forgot a crucial document for the supplier audit presentation, and the team is already behind schedule due to his earlier delay reviewing a corrective action plan. This scenario, unfortunately, isn’t uncommon for SQEs juggling various demands[…]
How Supplier Quality Audits Drive Zero Defect Manufacturing
The concept of “zero ppm” (parts per million) or “zero defects” has been around since the 1960s. It represents a continuous pursuit of excellence in manufacturing and development processes. Achieving “Zero Defect” translates to significant benefits – reduced costs associated with failure and increased revenue through enhanced customer satisfaction. While applicable to any organization, zero[…]
Unlocking Business Excellence: A Guide to ISO 9001 and Internal Audits
Over a million organizations worldwide trust the ISO 9001 Quality Management System (QMS) to achieve consistent success. This globally recognized standard helps businesses deliver products and services that consistently meet customer expectations, ultimately driving satisfaction and loyalty. ISO 9001’s versatility is a key strength – it can be applied by any organization, regardless of size,[…]
Regulatory Changes in the Automotive Industry in 2024
As you may already know, IATF 16949 is one of the most widely used standards for improving quality management systems and reducing defects and waste in the automotive industry. The International Automotive Task Force (IATF) announced that the 6th edition of the Rules for Achieving and Maintaining IATF 16949 certification would be published on March[…]
The Power of Engagement: How a Proactive QA Team Conquers Nonconformances and CAPAs
In the world of manufacturing, quality is everything. Even minor deviations from specifications, known as nonconformances, can have a ripple effect, impacting product safety, functionality, and ultimately, customer satisfaction. This is where a highly engaged Quality Assurance (QA) team steps in. The Challenge of Nonconformances Nonconformances can arise at various stages of production due to[…]
Understanding Deviations (Issues) in Manufacturing: The Second Class of Non-Conformances
In the relentless pursuit of quality, manufacturing thrives on consistency and adherence to specifications. However, even the most well-oiled production line can encounter hiccups. This is where the concept of non-conformances comes in. But not all non-conformances are created equal. This article delves into the second class of non-conformances, often termed deviations or issues, in[…]
In-depth on CFR 11
The U.S. Food and Drug Administration (FDA) plays a vital role in protecting public health by regulating medical devices. Part 11 of Title 21 of the Code of Federal Regulations (CFR) lays out the FDA’s requirements for electronic records and electronic signatures used by medical device manufacturers. Implications of CFR 11 This regulation ensures the[…]
Subscribe to our newsletter.
Your go-to destination for insights, best practices, and innovative solutions in supplier quality assurance.Recent Posts
IMDS: A strategic tool for supplier quality engineers
October 16, 2024
ABC on ISO/IEC 17025 Calibration Certificates
October 14, 2024
What is surface finish measurement and how it improves product performance
September 28, 2024
Optimizing Measurement Uncertainty for Enhanced Product Quality
September 25, 2024
Tags
ANSI
ANSI/ASQ Z1.4
AS9100
audits
automotive industry
CLM
contract lifecycle management
customer satisfaction
cybersecurity
data analysis
IATF
IEC 17025
imds
incoming inspections
Internet of Things
IoT
ISO
ISO/IEC 17025
ISO 9001
ISO 13485
manufacturing
Nonconformances
ppap
PPAP Management
PPAP regulations
problem solving techniques
QA regulations
quality assurance
quality control
quality technologies
REACH
risk management
SCARs
sqes
supplier audit
supplier audit checklist
supplier audits
supplier compliance
Supplier Quality
supplier quality engineers
Supplier Quality Management
supply chain
surface finish measurement
VDA
VDA Auditor
Let's talk to see how PPAP Manager can help your company to save time and money.