SBS - The best value in QMS software

The Original "Introductions" Thread started in 2001 and split off October 2009

Status
Not open for further replies.

Jim Wynne

Staff member
Admin
Re: New Folks - Please Take a Minute and Introduce Yourself / Say Hello!

QAMMAN said:
Greetings all,

Ok I'm going to break down and get involved.
I have been using the site now for a few months and have found it very helpful.

I am the Quality Assurance Manager, Management Rep, and Production Scheduler (I know, seems like a conflict of interest) at a small (40 employees) sheet metal manufacturing company in suburban Detoit.

We have been QS now for about 6 years and are pursuing TS registration.

I am down to writing my last procedure for Preventive Actions.

I hate this one because I have always said that a P/A could be written as a Continuous Improvement or a Preventive Action. (I know that I will get conflicting statements on that one LOL)

I have read many postings that have said they combined the C/A and P/A forms as one. It occurs to me that would work fine for QS but not TS.

TS requires a seperate procedure for P/A's and C/A's. I am making the assumption that the two procedures should not be mirror immages of each other so how could the forms be.

One think I like is that TS does not require a procedure for Continuos Improvements but says you will continuouslly improve the QMS.

I am reading this as saying through the correvtive action and preventive action process you are continuouly improving the QMS.

One last point, wouldnt corrective action address root cause more closely than preventive actions? If you are trying to prevent an occurance how would you have a root cause already?

I had a 3rd party internal audit a while ago (that turned into a gap analysis audit because it went so bad) and the auditor told me I need to address root cause as part of preventive actions. I do not see this as part of the standard and do not agree with her.

all opinions are welcome

kindest regards

the QAMMAN
Welcome to the Cove:agree1:

You should start a new thread (or threads) in the appropriate forums, rather than posting question here in this get-acquainted thread.
 
Elsmar Forum Sponsor

Wes Bucey

Prophet of Profit
Re: New Folks - Please Take a Minute and Introduce Yourself / Say Hello!

Welcome to all the new folks!:bigwave:

A more pleasant Forum experience:
Just a reminder to take a look at the threads in the Forum (How To Use the Forum Software - Basic Instructions) to help you with your posting of new threads.

Tell us more about yourself:
Even after a few years, I am still surprised at the geographic distribution of our visitors. Why not take the opportunity to add your location to our growing database? Read this thread to learn how:
Where are you from? Frappr mapping.
or go directly to
http://www.frappr.com/elsmarcove
 
F

fibanks

Mr

1. Fidelis Bankpegluu
2. Financial Administrator
3. Humanitarian Services sectors with NGO
4. have been working in this organization for 4 years
5. I do quality checks in financial reports and budgets
6. I will expect all top amangement of organizations to get involved in understanding budgets and the variance analysis against expenditures
 
A

atchukorn - 2011

Hello everyone,

elsmar.com is contain more knowledge and helpful for everyone interested in the quality. I had written my resume inthis web sit many day ago. I'm the freelance auditor for TS16949, QS9000, EMS and OHSAS. I stay in Thailand. You can reach me by 09-177-6290 if you visit Thailand. Warm Welcome to you.

Thanks and love elsmar.com,

Rgds,

Atchukorn T.
 
C

Craig H.

Hello, all.

The international flavor of this site amazes me. What also amazes me is that even in different cultures, quality professionals face the same kinds of issues!

Anyway, WELCOME!!! Glad you joined us!

Craig
 
Q

Quality

Re: New Folks - Please Take a Minute and Introduce Yourself / Say Hello!

1. Louise
2. Quality Assistant
3. Manufacturing
4. Olsen Engineering, Iowa
5. 4 months
6. I've never worked in anything other than food service or as a receptionist, and I love my job so much I am changing my degree program to Industrial Engineering
7. People have been working at their job for so long they fall into the "this is the way we've always done it" attitude. We have 3 new people in our quality department (there are 4 of us total), so we have fresh ideas & can see what isn't working since we are new eyes.
8. Have people understand that yes, efficiency is important, but having a lot of parts is not good if they are bad quality.
 
R

robertlau

Re: New Folks - Please Take a Minute and Introduce Yourself / Say Hello!

Hello, this is Robert Lau from HK.
I've been in the Quality field for 11years after graduated from my Electronic Engg. Bachelor Degree.

Now I'm working in an international electronics company which supplying OEM/ODM products to Automotive customers.

Wish to learn from other quality experts worldwide.
 
M

Markku

Re: New Folks - Please Take a Minute and Introduce Yourself / Say Hello!

It's not a bad Idea, even if I'm an "old new" member. I was member allready in 1998, so after having implemented my first QS-9000 system in 1995, so it was a little bit too late to ask help.

1. Markku Ruokanen
2. Quality Director
3. Industry? From Stainless Steel to Electronic and Semi-conductor business passing a while in Medical Devices and independent and now back to Electronic Components. From Start-Up to a SME-size companies. The red-line has been Technology, Automotive and Quality.
4. Maxwell Technolgies, Rossens CH
5. General ISO experience since 1987, Automotive (VDA, QS-9000, EAQF, and ISO-TS 16949) since 1994 and 3 years experience of the ISO-13485 and related EU and FDA stuff.
6. I'm a grazy Finn.
7. Keep it simple!

Regards

Markku
 
Status
Not open for further replies.
Thread starter Similar threads Forum Replies Date
E Original Brand Labeler (OBL) in China China Medical Device Regulations 2
N Original signed IQ/OQ/PQ missing - but have data - Do we do it over? ISO 13485:2016 - Medical Device Quality Management Systems 2
T More than One Original Test Report - Original Print General Measurement Device and Calibration Topics 4
P Who is the OEM (Original Equipment Manufacturer)? EU Medical Device Regulations 5
G Original Data Copying to Maintain Compliance with 21 CFR Part 820.180 US Food and Drug Administration (FDA) 2
F Can you reference original FAI (First Article Inspection) after Delta? AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 3
V Supplier Moving Manufacturing Location after original PPAP APQP and PPAP 4
T Stamping Original Paper Document 'Record Copy' in Red Ink - Document Control Document Control Systems, Procedures, Forms and Templates 4
H ISO 9001:2000 Certificate - Original approval date 18 July 1995 and valid until 2012 ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 27
Q OEM (Original Equipment Manufacturer) PPAP Applicability Query IATF 16949 - Automotive Quality Systems Standard 4
P Benchmark of OEM (Original Equipment Manufacturer) Sourcing Audit Process Audits and Layered Process Audits 8
Marc "This American Life" reveals original Coca-Cola recipe World News 0
G OEM (Original Equipment Manufacturer) Calibration of In-House Measurement Equipment General Measurement Device and Calibration Topics 18
S Reference to original Calibration Certificate - ISO 17025 Section 5.10.9 ISO 17025 related Discussions 4
P Medical Device OEM (Original Equipment Manufacturer) Agreements Other Medical Device and Orthopedic Related Topics 5
P What's the original definition of "sigma level"? Capability, Accuracy and Stability - Processes, Machines, etc. 1
D Training Records - Requirement to keep original copy of training/assessment form? Records and Data - Quality, Legal and Other Evidence 12
Stijloor OEM (Original Equipment Manufacturer) Requirements for Global MMOG/LE Completion Customer and Company Specific Requirements 15
M Original written signatures vs. Copies/scans/faxes/electronic documents US Food and Drug Administration (FDA) 24
W Requirement to save original, handwritten internal audit notes? US Food and Drug Administration (FDA) 11
J Required to put original manufacturers on Approved Supplier List? Supplier Quality Assurance and other Supplier Issues 6
T Monthly SPC original data sheets - What should be done with the reports? AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 9
L Original Documentation - Need to maintain any original hand written documents ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 28
E [Ask] Original Equipment Manufacturing/Manufacturer Misc. Quality Assurance and Business Systems Related Topics 1
S Definition OEM (Original Equipment Manufacturer) - Exact definition of OEM Definitions, Acronyms, Abbreviations and Interpretations Listed Alphabetically 9
D Can we destroy original paper files before retention period if we scan them? Records and Data - Quality, Legal and Other Evidence 17
Marc Reporter Discovers People Living In Original Star Wars Set Coffee Break and Water Cooler Discussions 4
Marc 40th Anniversary of the original Star Trek - From the I'm Getting Old Department World News 22
M Is TS16949 Only for OEM (Original Equipment Manufacturer) Customers? IATF 16949 - Automotive Quality Systems Standard 8
J Internal Audit Reports - Mandatory to keep original paper copy? Internal Auditing 16
R Retention of records - Original Order Form vs. Computer Entry record - ISO 13485 Records and Data - Quality, Legal and Other Evidence 12
D Need to get ISO recertified for a site change, but just near to the original site? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 3
Q European Legislation 76/769/EEC - Seeking the original legislation Various Other Specifications, Standards, and related Requirements 4
B Honda - What's different from US OEM (Original Equipment Manufacturer) requirements? Customer and Company Specific Requirements 4
C Procedures - New Revision or Original Issue - Upgrading to ISO9001:2000 ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 3
V Definition OEM - Definition of OEM - Original Equipment Manufacturer Definitions, Acronyms, Abbreviations and Interpretations Listed Alphabetically 8
Raffy Calibration Labels - Original Calibrating Date or New Date? General Measurement Device and Calibration Topics 9
V In-House Calibration vs. OEM (Original Equipment Manufacturer) Calibration General Measurement Device and Calibration Topics 2
D PPAP Master Parts - Do we have to save the original PPAP parts? APQP and PPAP 2
M Informational EU – Eudamed Data exchange services and entity models introductions Medical Device and FDA Regulations and Standards News 4
D Accurately measuring Full Thread Length Inspection, Prints (Drawings), Testing, Sampling and Related Topics 11
DuncanGibbons Additive Manufacturing Processes Thread Manufacturing and Related Processes 5
V Thread Plug Gage Pitch GO Diameter out of spec AQL - Acceptable Quality Level 8
C Aluminum galling on thread plug gauge Manufacturing and Related Processes 10
ScottK Measuring thread flank angle on a screw Inspection, Prints (Drawings), Testing, Sampling and Related Topics 1
G Oversized Threads - What sized stab pin would be best to quickly check for oversized thread holes General Measurement Device and Calibration Topics 5
H Thread Plug Gauge Tolerances General Measurement Device and Calibration Topics 3
A Cost effective thread gaging with ISO 9001 ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 2
APHX02 Thread Roll Process Verification w/in AS9100 (i.e. BSP-F-69/AS8879) Manufacturing and Related Processes 2
C Thread Tolerance - Can I use a 3A Ring on a part that the drawing calls out for a 2A? Manufacturing and Related Processes 5

Similar threads

Top Bottom