Who is Approving your Manufacturing Visual Aids / Process Sheets?

Elsmar Forum Sponsor

CarolX

Super Moderator
Super Moderator
#2
Re: Who is approving your Manufacturing Visual aids/process sheets?

Hi!
Who is approving your manufacturing visual aids or process instructions?
Thanks for your reply.
At our facility - engineering is responsible for all work instructions for manufacturing.
 
W

wmarhel

#3
Re: Who is approving your Manufacturing Visual aids/process sheets?

Hi!
Who is approving your manufacturing visual aids or process instructions?
Thanks for your reply.

It needs to be the workers and/or the people who will be utilizing them. If they can't understand the tasks required, how can you expect them to be followed?

Wayne
 

shrikantborkar

Starting to get Involved
#4
HI
Production Engineering head approves the Work Instructions. other than Process Discipline WI can be Approved By Production manager.

Products constructions WI is O/p Design Process.

we Release in meeting and Explain to Operator and Their Lead.

Normally encourage Operators to find difference between WI and what they do?
i.

Regards
Shrikant
 

Ajit Basrur

Staff member
Admin
#5
Agree with others - typically, it is approved by Production personnel however it could vary from one organization to another.
 
S

Sequence_Barry

#6
Our experience has been that it depends heavily on the industry. In highly regulated industries such as military, aerospace, med-device, there may be many approval levels for work instructions. Even within these industries, it can vary depending on the criticality of the affected part. The other extreme is that manufacturing engineers in some organizations have the ability to author and approve their own work.
 
Thread starter Similar threads Forum Replies Date
C Approving AWS as a supplier (ISO 13485) ISO 13485:2016 - Medical Device Quality Management Systems 4
M Suitable form or questionnaire for approving consultants Document Control Systems, Procedures, Forms and Templates 9
N Understanding, Challenging & Approving Supplier Control Plans FMEA and Control Plans 7
R Question of Approving Documents ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 1
JoCam Approving a Test House on a Medical Device as a part of a 510k Submission 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 3
Q Approving Software Suppliers in an AS9100 Company AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 5
R Approving a New Hand Assembly Line at a Supplier Inspection, Prints (Drawings), Testing, Sampling and Related Topics 1
R Approving Suppliers by "Grandfathering" ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 14
N Role of Quality Function in Approving Work Instructions Document Control Systems, Procedures, Forms and Templates 4
Q AS9100 Clause 8.3 - Control of Nonconforming Product Process for Approving Personnel AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 1
T Approving Consulting Firms in a Medical Device Company ISO 13485:2016 - Medical Device Quality Management Systems 25
T Approving Suppliers - Approving Marketing Companies Other ISO and International Standards and European Regulations 10
P Originating and Approving Internal Procedures Document Control Systems, Procedures, Forms and Templates 9
L Approving myself as a Supplier - Should we be on our own ASL AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 10
M Gage R&R for Big Parts - Approving a Variable Gage using only 1 Part Gage R&R (GR&R) and MSA (Measurement Systems Analysis) 7
G Does AS9100 require approving your Customer as a Supplier? AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 8
J Re-approving documents when the responsible person leaves or changes responsibilities ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 14
A Qualifying and Approving Equipment for Welding AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 3
A Process for Approving Personnel Making Decisions - AS9100 Clause 8.3 AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 8
B Approving Suppliers - Consultants AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 8
J Approving Suppliers under 7.4.1 - Approved Suppliers List - ISO 9001:2000 ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 4
T Approving Suppliers under 7.4.1 - AS9100 AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 20
T Approving documents prior to issue - What guarantees their adequacy? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 12
S CE and Manufacturing license Manufacturing and Related Processes 1
S Manufacturing Process FDA FOIA Medical Device and FDA Regulations and Standards News 3
S Manufacturing Process FDA FOIA US Food and Drug Administration (FDA) 4
S Critical characteristic on manufacturing operations test procedure Inspection, Prints (Drawings), Testing, Sampling and Related Topics 0
P ISO 8 classified medical manufacturing room Qualification and Validation (including 21 CFR Part 11) 1
P How to measure DPPM in Chemical batch manufacturing Quality Tools, Improvement and Analysis 1
M MSA Study Type 1 not capable. We are at the limit. And manufacturing wants to continue producing. Gage R&R (GR&R) and MSA (Measurement Systems Analysis) 7
J Calibration cycle for monitoring & measuring tools used in medical device manufacturing General Measurement Device and Calibration Topics 5
M Office and manufacturing site relocation effect on Device Technical File CE Marking (Conformité Européene) / CB Scheme 2
lanley liao How to keep the manufacturing capability under the API monogram Oil and Gas Industry Standards and Regulations 6
O Any info on release date of FDA “Computer Software Assurance for Manufacturing and Quality System Software” document? 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 0
Ed Panek What are the limits on manufacturing changes and substantial changes? EU Medical Device Regulations 6
Z Rapid audit template for plastic parts manufacturing process Manufacturing and Related Processes 12
P IQ, OQ, PQ protocol, and report templates for Distributed Control Systems in Pharmaceutical Manufacturing Systems. Qualification and Validation (including 21 CFR Part 11) 0
K One CE Mark holder - multiple manufacturing sites EU Medical Device Regulations 3
M Indian Medical Device Rules - Manufacturing and Wholesale Lic. Required? Other Medical Device Regulations World-Wide 12
R Manufacturing plants relocation - Medical Device Medical Device and FDA Regulations and Standards News 7
R Medical Device - Change manufacturing plant Design and Development of Products and Processes 6
P New Global HQ Suggestions for Virtual manufacturing/own brand labelling of medical devices? EU Medical Device Regulations 4
S Manufacturing Execution Systems Software Costs Manufacturing and Related Processes 0
P Managing How PPAP Requirements are Communicated in the Manufacturing Process and to Suppliers APQP and PPAP 5
J Control Plan use on the manufacturing floor FMEA and Control Plans 4
S PSW - Requirements for "off-the shelf" component that has multiply manufacturing locations Off the Shelf Item Manufacturing and Related Processes 1
DuncanGibbons Additive Manufacturing Processes Thread Manufacturing and Related Processes 5
S Can assembly manufacturing sub-supplier be certified IATF 16949? IATF 16949 - Automotive Quality Systems Standard 6
A ISO 14971 PFMEA Manufacturing Risk ISO 14971 - Medical Device Risk Management 2
L Manufacturing Process Audit Help IATF 16949 - Automotive Quality Systems Standard 6

Similar threads

Top Bottom