SBS - The best value in QMS software

Clarification on TS 16949 Clause 8.2.3.1 - "... availability..."

S

srcskrishnan

#1
Good Morning,:confused:

I am new to posting. Meaning that I am posting first time.

I hv a clarification in one of the TS 16949 clause

In Clause 8.2.3.1..........."These documents shall include objectives for manufacturing capability, reliability, maintainability and availability, as well as acceptance criteria".

Here I would like to know what does "availability" means.

Sankrish
 
Elsmar Forum Sponsor
T

tbsiva

#2
Re: Clarification on TS 16949 clause 8.2.3.1 - "......... availability..."

As I understand, Availability means machine up time. Availability = Available Time / Scheduled Time.
Example:
A given Work Center is scheduled to run for an 8 hour (480 minute) shift.
The normal shift includes a scheduled 30 minute break when the Work Center is expected to be down.
The Work Center experiences 60 minutes of unscheduled downtime.
Scheduled Time = 480 min - 30 min break = 450 Min
Available Time = 450 min Scheduled - 60 min Unscheduled Downtime = 390 Min
Availability = 390 Avail Min / 450 Scheduled Min = 90%

By overall, u should have action plan to reduce break down hours
 
S

srcskrishnan

#3
Re: Clarification on TS 16949 clause 8.2.3.1 - "......... availability..."

As I understand, Availability means machine up time. Availability = Available Time / Scheduled Time.
Example:
A given Work Center is scheduled to run for an 8 hour (480 minute) shift.
The normal shift includes a scheduled 30 minute break when the Work Center is expected to be down.
The Work Center experiences 60 minutes of unscheduled downtime.
Scheduled Time = 480 min - 30 min break = 450 Min
Available Time = 450 min Scheduled - 60 min Unscheduled Downtime = 390 Min
Availability = 390 Avail Min / 450 Scheduled Min = 90%

By overall, u should have action plan to reduce break down hours
Thanks tbsiva,

That was very helpful.

Sankrish
 
R

rickmcq

#4
Re: Clarification on TS 16949 clause 8.2.3.1 - "......... availability..."

May I ask what that following, in the same element, means?

"Significant process events, such as tool change or machine repair, shall be recorded"

I'm thinking that "tool change" means machine tool as opposed to a cutting tool.
 

Stijloor

Staff member
Super Moderator
#5
Re: Clarification on TS 16949 clause 8.2.3.1 - "......... availability..."

May I ask what that following, in the same element, means?

"Significant process events, such as tool change or machine repair, shall be recorded"

I'm thinking that "tool change" means machine tool as opposed to a cutting tool.
ISO/TS 16949:2009 is not concerned about normal perishable tooling such as drill bits, inserts, milling cutters, etc. However, any changes and repairs on machine tools, jigs, fixtures, other work holding devices, etc., must be recorded.

Stijloor.
 
R

rickmcq

#6
Re: Clarification on TS 16949 clause 8.2.3.1 - "......... availability..."

ISO/TS 16949:2009 is not concerned about normal perishable tooling such as drill bits, inserts, milling cutters, etc. However, any changes and repairs on machine tools, jigs, fixtures, other work holding devices, etc., must be recorded.

Stijloor.
Thank you. How were you able to figure out it means fixtures, jigs, etc. by the way the element is worded? :bonk:
 

Stijloor

Staff member
Super Moderator
#7
Re: Clarification on TS 16949 clause 8.2.3.1 - "......... availability..."

Thank you. How were you able to figure out it means fixtures, jigs, etc. by the way the element is worded? :bonk:
Thank you! Common sense and many years of experience! "Tooling" must be viewed and interpreted in the context of an automotive parts and materials manufacturing process such as machining parts, assembling components, sewing interior carpet, dying fabrics, stamping sheet metal, injection molding, etc.

Stijloor.
 

Marc

Hunkered Down for the Duration with a Mask on...
Staff member
Admin
#8
Re: Clarification on TS 16949 clause 8.2.3.1 - "......... availability..."

ISO/TS 16949:2009 is not concerned about normal perishable tooling such as drill bits, inserts, milling cutters, etc. <snip>
Even there, most companies do keep track of (read 'records of') perishable tooling in one way or another whether required by TS 16949 or not.
 
R

rickmcq

#9
Re: Clarification on TS 16949 clause 8.2.3.1 - "......... availability..."

ISO/TS 16949:2009 is not concerned about normal perishable tooling such as drill bits, inserts, milling cutters, etc. However, any changes and repairs on machine tools, jigs, fixtures, other work holding devices, etc., must be recorded.

Stijloor.
What about 7.5.1.5 Management of Production Tooling where it mentions "tool change programmes for perishable tools"? I realize it doesn't specifically mention "records" in the element.
 

Stijloor

Staff member
Super Moderator
#10
Re: Clarification on TS 16949 clause 8.2.3.1 - "......... availability..."

What about 7.5.1.5 Management of Production Tooling where it mentions "tool change programmes for perishable tools"? I realize it doesn't specifically mention "records" in the element.
That's part of what we used to call "process control", and process control instructions may dictate when perishable tools must be changed. Records of these events are not required unless requested by the organization for the purposes of statistical process control, because in some circumstances, changes may affect the behavior (stability) of the process.

Stijloor.
 
Thread starter Similar threads Forum Replies Date
F TS 16949 Clause 7.2.1 - Note 2 - Recycling program - Clarification IATF 16949 - Automotive Quality Systems Standard 4
M Request for clarification on TS 16949 Clause 5.6.1.1 IATF 16949 - Automotive Quality Systems Standard 5
T Clarification for ISO/TS 16949 Clause 7.5.1.5 & 7.5.1.6 IATF 16949 - Automotive Quality Systems Standard 1
T Clarification of TS 16949 Clause 7.1 IATF 16949 - Automotive Quality Systems Standard 4
M TS 16949 - Request for clarification on clause 6.4.1 IATF 16949 - Automotive Quality Systems Standard 4
M TS 16949 - Request for clarification on the first paragraph of clause 7.5.5.1 IATF 16949 - Automotive Quality Systems Standard 1
M Analysis and Use of Data clarification - TS 16949 Clause 8.4.1 IATF 16949 - Automotive Quality Systems Standard 4
M Request for clarification on TS 16949 clause 8.4 IATF 16949 - Automotive Quality Systems Standard 3
M TS 16949 Clause 8.2.3.1 M/M of Manufacturing Processes Clarification IATF 16949 - Automotive Quality Systems Standard 3
M TS 16949 Clause 7.6.3.1 - Internal Laboratory - need clarification IATF 16949 - Automotive Quality Systems Standard 3
M Request for clarification on TS 16949 Clause 7.2.2.2 IATF 16949 - Automotive Quality Systems Standard 3
R ISO/TS 16949:2009 Clause 4.1 General Requirements (Outsourcing) Clarification IATF 16949 - Automotive Quality Systems Standard 6
D Clarification on "Customer Property" - TS 16949 Clause 7.5.4 IATF 16949 - Automotive Quality Systems Standard 4
M Clarification on Calibration/Verification Records 7.1.5.2.1d (IATF 16949) General Measurement Device and Calibration Topics 11
D Clarification of Applicability of TS 16949 Requirements to a Non-Automotive Business IATF 16949 - Automotive Quality Systems Standard 13
M Calculating the IATF TS 16949 Recertification Audit Man Days - Clarification ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 6
M ISO/TS 16949 Cl 7.5.1 a) - Characteristics of the Product - Need Clarification IATF 16949 - Automotive Quality Systems Standard 4
qualprod D5 of 8D clarification, how to verify root cause Problem Solving, Root Cause Fault and Failure Analysis 26
K IPC-610 Section 10.4.2.2 clarification - Distance to be measured Various Other Specifications, Standards, and related Requirements 0
M Off-Label Use - Clarification of FDA Policy US Food and Drug Administration (FDA) 1
T Implant Card - Article 18.1(a) and MDCG 2019-8 clarification EU Medical Device Regulations 3
Q Need clarification on requirements.... Class i, gmp & 510(k) exempt Medical Device and FDA Regulations and Standards News 12
M Informational TGA Consultation: Proposed clarification of the regulatory requirements for medical device systems and procedure packs Medical Device and FDA Regulations and Standards News 2
R ASQ reference material clarification - Spiral bound materials allowed in ASQ Exam? Professional Certifications and Degrees 1
Q ISO 3310 Clarification Help - Aperture sizes for sieves used for particle sorting Other ISO and International Standards and European Regulations 2
S The Severity of a Medical Device Hazard - Risk Analysis Clarification ISO 14971 - Medical Device Risk Management 6
M 8.3.2.3 Development of products with embedded software - request for clarification IATF 16949 - Automotive Quality Systems Standard 1
M FDA News USFDA Draft Guidance – Clarification of Radiation Control Regulations for Manufacturers of Diagnostic X-Ray Equipment Medical Device and FDA Regulations and Standards News 0
T Clarification on MDR - Article 18(d) - Implant Card EU Medical Device Regulations 14
S QS, RS deflection - clarification wanted IEC 60601 - Medical Electrical Equipment Safety Standards Series 0
A ISO 2859 Single Sampling - Clarification regarding the sampling table Inspection, Prints (Drawings), Testing, Sampling and Related Topics 4
S Requirements for Interval Measurement test & Frequency Response test clarification IEC 60601 - Medical Electrical Equipment Safety Standards Series 0
S Clarification regarding tests in IEC 60601-2-25 IEC 60601 - Medical Electrical Equipment Safety Standards Series 1
J Internal Audit clarification - How to perform the audits IATF 16949 - Automotive Quality Systems Standard 6
V Clarification - Hydrogen De-embrittlement Manufacturing and Related Processes 6
K UDI Direct Marking Compliance Date Clarification and one other UDI question Other US Medical Device Regulations 0
N Applied Parts Classification Clarification - Breast Pump IEC 60601 - Medical Electrical Equipment Safety Standards Series 1
V Clarification of Injection part shrinkage ratio Manufacturing and Related Processes 1
J ISO 9001:2015 8.2.3 - Review of Requirements (Clarification on compliance) ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 8
B Health Canada Recall Definition - Seeking Clarification Canada Medical Device Regulations 5
Q ISO 9001:2015 - Clarification in 6.1.2 Note 1 (Options to Address Risks) ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 6
S Clarification of threaded ring gage calibration procedure/requirements General Measurement Device and Calibration Topics 2
B Clarification on interpretation of some EN ISO 14971:2012 & IEC 62304:2006 req's ISO 14971 - Medical Device Risk Management 46
S AS9102 - Clarification - PO asking for an Assembly at Rev B (Print at Rev C) AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 3
Pmarszal Clarification for 21 CFR Part 11.100 - General Requirements Other US Medical Device Regulations 14
B Clarification of ISO 9001:2015 Clause 8.5.6 Control of Changes ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 11
M Integrated Phased Processes - AS9100D cl. 8.1 Operational Planning - Clarification AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 8
A Monitoring and Measuring Resources (7.1.5) - Clarification ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 3
dubrizo Clarification Requested in 6.2.2 ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 7
K EN ISO 15223-1:2012 Clarification or Examples on when to use Safety Symbols Other Medical Device Related Standards 3

Similar threads

Top Bottom