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Goods in transit using 107 & 109 mvmt types

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Dear All,

 

As per our business requirement we are using movement types 107 and 109.

 

When I post with 107 into valuated GR-blocked stock when the ship is loaded,Inspection lot is created. We do UD with Accepted and Invoice payment down without stock transfer, then we do 109, again Inspection lot is created. now we are doing stock transfer to own stock.

 

Our client requirement  is

 

1. Dont want stock transfer tab for lot created by 107. but required for 109.

2. Or while doing 109, no inspection lot generate.

3. dont require two inpsection lots from 107 and 109.

 

 

Regards


Lots in QA32 & QA16

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Hi,

 

 

I need a help related to issue of inspection lots of calibration equipment. In QA32 all inspection lots are reflecting but with the same input criteria, only one lot is getting reflected in QA16 tcode. User wants to finish pending lots with only UD.What could be the possible reason for this.

CRTD status not getting relese for callibration order (Order type PM05)

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Dear All,

 

My Inspection lot CRTD status still not getting release for callibration order (Order Type PM05)

 

Created Inspection lot is assigned to task list but in QA32 lot status still showing CRTD

 

Thanks

Abhishek

Task Determination in Quality Notification Issue

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Hi Gurus,

 

 

We are facing a issue regarding quality notification, in normal condition when we put required values like Defect Type, Priority etc. when we click Task Determination, it generates 2 investigation tasks & 6 Customers tasks, but there are issue for some material, system creating 46 investigation tasks & 10 customer tasks. Can you please help.

 

 

Regards,

Pankaj

QM-CoA, repack material form bulk need to refer bulk lot for printing specifications

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Hi All,

 

I hope I can get answer here, as I need some help from experts for the below process.

 

Scenario 1:

Bulk material is manufactured at site A, during GR inspection lot is created manually  89 ins type and then shipped to site B, we have done the enhancement to copy the results from site A inspection lot to Site B inspection lot. No problem here.

 

Then the same bulk material is repacked at receiving site(Site B) to ship to customers, now we need to print CoA where we need to pick the results from the bulk inspection lot(Site B where we copied from Site A).I know we have the option in certificate profile to choose the function module"batch from production chain" but this is not working as we received bulk material form different plant and not manufactured at same plant.

 

So we tried to develop custom program to pick the results from bulk inspection lot, the challenge is repacking(bulk to packed) is done by using planned order, so we can't able to trace the source batch(bulk), the issue is we cant able to trace the batch from planned orders if we know how to get the batch information linking planned order(the reason is only planned order has information of bulk material and packed material) then we can able to identify the inspection lot based on bulk material/batch and pick the results .

 

Scenario 2:

 

Bulk material is manufactured at same plant, but during GR they create manual inspection lot 89. Finally they repack it to packed material where we need to pick the results from bulk material inspection lot. The issue is again we can't use the function module in certificate profile to pick the results from production chain due to inspection type 89 which is non stock relevant and no integration with process/planned orders. I think when we identify the solution for scenario-1 then we can able to solve this too.

 

I really appreciate your help to throw some light on this. Thanks in advance,

 

Cheers,

Chid.M

How to make field as input,required,display only and hidden.

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I have seen most of question related to make some field display, hidden and input only. So this document helps them to make desired file disable and input as per the requirement without using screen variant and transaction variant.

 

 

Go to that screen onto which you want to make any field disable, input and hidden. Then Select System-Status and copy the program name from there.

Hidden.png

Then Go to t-code OQFA and the give Module Pool name as program name.Then click on change It will reach you at Field Selection Screen Group.Then select the desirable screen group and click on Modifiable. and make the desirable field as input display and hidden.

You can use Influencing Button if you want these change to particular thing like inspection type, notification type.

 

OQFA.png

 

Screen group.png

Fields.png

Error in QC03?

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Dear All QM experts,

 

please help me to solve below error on urgent basis. Previously this error was not arises but from 3 days it is showing same error for all. I have checked Inspection lots in QA32 for the same 

 

In QC03 transaction,

 

I have given Input Cert. Profile, Version and Certificate Type.

 

Then Enter and system displayed Header data screen. On this screen select Certificate View .

 

Now get screen Delivery selection for simulation, In this screen entered Delivery no., item and ship to party/sold to party.

 

Now when click on  Certificate view then system displayed an below error

 

  No lot was found for cert.profile E31A ST23_02  000001, material
  No lot was found for cert.profile E31A ST23_02  000001, material

  The specifications for characteristic 0003 were not found in batch 31

  The specifications for characteristic 0004 were not found in batch 31

  The specifications for characteristic 0005 were not found in batch 31

 

Thanks,

Naresh

Restrict UD when user put quantity in Scrap field.

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Hi All,

 

 

In QA32 transaction, before UD for the inspection lot, if user place the stock in SCRAP then system should not allow him until an approval get from authorized person.

 

How to map this scenario by user status profile.

 

 

 

 

Thanks,

Parag


Restrict scrapping in QA32

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Dear Experts,

 

We need to have user wise restrictions for scrap posting through QA32 while giving the UD. This means only some users should have the right for scrapping in QA32. We have blocked movement type 553 using basis object M_MSEG_BWA-BWART. But this is working in MB1A only. Please provide some guidance.

Thanks in advance.

 

Regards,

Jeewana

"Responsible" field greyed out in IQS1 transaction

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Hi Experts,

 

In IQS1 transaction, if I am trying to create a custom notification , then the "Responsible" field is grayed out.

How can I make this field "Input enabled"?

 

Please refer below screen:

iqs1.PNG

I tried making this field "Input" in OQM1, but no result!

 

Any user exit to modify this field?

 

Regards,

 

Narsingh

Control Inspection Lot

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Hello QM Gurus,

 

What is the best option to suggest / choose from the "control insp lot" for apparel industry with batch management active?

 

BR,

 

@rul

Add Material classification field in QA32 ALV

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I want to add Material Classification Field in QA32 and QA33 ALV screen. What is the method?

Custom fields with BAPI_QUALNOT_CREATE and BAPI_QUALNOT_MODIFY_DATA

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I added custom fields to QM Notifications with enhancement QQMA0001.  They work fine with QM01, QM02 and QM03.

 

Now I need to create and change Notifications with an interface; including the custom fields.

 

Is there a way to populate custom fields with the QM Notification BAPI's?

 

BAPI_QUALNOT_CREATE

BAPI_QUALNOT_MODIFY_DATA

 

If no, are there other function modules that will do this?

 

Regards,

Mark

Characteristic xxxxx from FMEA xxx is not part of the control plan

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Dear All,

 

 

 

When i am giving FMEA in Control Plan am getting the error "Characteristic COLOR from FMEA LID is not part of the control plan".All the characteristics which are part of my FMEA are not getting adopted to Control Plan and getting the same error in consistency check of control plan .Please help me in resolving this issue for effective utilization of FMEA Cockpit.

 

 

Thanks & Regards,

Chandra.

MIC hide to other user id while result recording

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Hi,

 

In QC dept. total 20 nos. of MIC. There are 2 user ID maintained in QC dept. Some MIC that are record by other user, having separate ID.

So I want to hide some Master Inspection Characteristic to other User ID that he don't use.

Please Suggest....


block payment for rejection

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Hi All,

 

I have one requirement.

I have one inspection lot for 10 qty, during usage decision 7 qty is put in unrestricted stock and 3 qty rejected and put "in new material" and moved to rejection location. As we can mot make partila UD fo one lot, i have made UD as accepted under minor concession. Now requirment is that during paymenent to vendor system should not allow to do for 10 qty, it should allow for 7 qty as it is moved to unrestricted. How can I do this?

 

Plz advice.

 

Thanks,

 

Regards,

Mayur Patil

To Generate the Inspection Lot on the basis of Counter

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Hello Experts,

 

I required to generate Inspection Lot on the basis of Counter for the Strip Test Process.

Strip Test is used in Pump Industry.

Process of Strip Test is as Follows:-

1. Pump To be Stripped by Quality Peoples after the Testing Operation from the production on the basis of the particular counter(For Example 1 out of 50 Pumps).

2. After Stripping the pump if the Quality is ok then pump is release for the next operation with defining particular identification(for example Like Serial number).

3. If Quality is not Ok for the Strip Test then that particular lot with all pumps will be put on hold for decision.

 

 

Thanks & Regards.


DIGITAL SIGNATURE WITH SIGNATURE STRATEGY—SIMPLE GUIDE

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DIGITAL SIGNATURE WITH SIGNATURE STRATEGY--Simple Guide

 

 

DIGITAL SIGNATURE WITH SIGNATURE STRATEGY—SIMPLE GUIDE

SAP has provided individual signatures and signature strategies in the following functions in Quality Management:

  • In the inspection lot: During results recording
  • In the inspection lot: At the usage decision
  • When confirming the physical-sample drawing. This means, when releasing the first physical sample in a physical-sample drawing.
  • For quality notifications

 

In this document we will deal with signature strategy in result recording with System Signature with Authorization By SAP User ID/ Password Method. It will show you signature strategy at two level. At UD we can use strategy with one level only. Multiple level is not supported at UD.

  1. 1.     Level 1—User who enter the result in SAP
  2. 2.     Level 2 –User who verifies the entered result.

 

Prerequisites

  1. 1.     Make sure that Enterprise extension EA-PLM must be activated.
  2. 2.     Activated Business Function  OPS_QM_EXTENSIONS. Business Function is available from SAP Enhancement Package 3 for SAP ERP 6.0. Without activating Enterprise extension you will not be able to activate this Business Function.

image1png.png

image2.png

 

After activating prerequisites, following Signature Strategy customizing node is available in config.

 

image3.png

STEP 1.  Create two authorization group one for Entry Level and One for Verification level.

QCC0->Quality Managment->Environment->Central Functions->Signature Strategy->Define Authorization Group

On the basis of authorization group we will control the user id  to execute the signature. Here Two Authorization group EING and VERIF is created.

image4.png

STEP 2.  Create Individual Signature and assign to authorization groups.

QCC0->Quality Managment->Environment->Signature Strategy->Define Individual Signature

 

image5.png

STEP 3.  Create Signature Strategy with Signature Method R(System Signature with Authorization By SAP User ID/ Password) and assign Individual Signatures.

QCC0->Quality Managment->Environment->Central Functions->Signature Strategy->Define Signature Strategy.

 

image6.png

 

image7.png

STEP 4. Create Signature Sequence in which signature must be executed.

QCC0->Quality Managment->Environment->Central Functions->Signature Strategy->Define Signature Strategy.

Select Signature Strategy and click on Signature Sequence Button. It is defined  here that M1 signature must be executed before M2 signature.

image8.png

STEP 4.  Create the release status  when both sign have been done.

QCC0->Quality Managment->Environment->Central Functions->Signature Strategy->Define Signature Strategy.

 

  Select Signature Strategy and click on Release Button and Check on release status

image 9.png

STEP 5. Create QM Material Authorization group ,Assignment of Strategy to Authorization Group

QCC0->Quality Managment->Environment->Central Functions->Define Authorization Groups and Digital Signature.

Here you can decide when you require Digital Signature, i required only at the time of result recording so i have done setting for that.

 

image10.png

And assign the signature strategy to SignStratRR

image11.png

Here we can assign different strategy to respective column according to the need as strategy for UD , Physical Sampling and Result Recording as per the requirement

 

Signature Type---- Select signature type for Result Recording. I have selected Asynchronous Signature Strategy with changeable Signatory. You can user as per requirement. Press F1 for help to know about other signature type.

 

image12.png

STEP 6. Define Signature Method for Signature Object Type.

QCC0->Quality Managment->Environment->Central Functions->Define Authorization Groups and Digital Signature.

 

image13.png

 

STEP 7. Assignment of QM Material Authorization to QM view of Material Master

image14.png

STEP 8. Create or Change two roles role1 and role 2 and Assign Authoirzation Objects(C_SIGN_BGR,C_SIGN).

T-Code ---PFCG.

Generally Functional Consultant don’t have this t-code rights. Take help of Basis Guy for above mentioned activity.

Assign Application and Signature Object for Result Recording as LOT and LOT_RR as show below and Give Atuhorization Group as VERIF  and EING in two roles respectively, which we have define earlier.

image15.png

image16.png

STEP 9. Assign those roles to respective User Ids eg. Let say role 1 to QM_TEST  and role 2 to Manish.

STEP 10. Create the lot of that material to which QM Material Authorization has been assigned and Do  result recording.

While closing the result it will ask for first level Signature.

image17.png

image18.png


STEP 11. For second level signature user t-code QEDS

image19.png

 


 

image20.png

 

Use Sign Button to verify each char one by one. We can sign all char by selecting all chars and then click on Sign Button.

Then it will ask for you second level signature. Only User id(Manish in eg.) which has authorization of VERIF authorization group will not be able to do the signature.

 

STEP 12.  For log purpose we can user t-code DSAL

 

image21.png









 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Results recording to be sent to vendor

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Hi,

 

After entering results recording in QA32, I want to send these results recording to vendor through email.

 

Please let me know how to achieve this? Any standard workflow or user exit can achieve this?

 

 

Regards.

QM cycle for Process orders

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Hello Gurus,

 

I have to implement following sequence control for process order ,Please guide how it can be done with least cutom developments.

Is there a Qc mechanism which will refer to previous Batch and check its QC parameters for on line inspection?? .

OR,...Is there any Process order Mechanism that checks previous Process order QC parameters for on line inspection?? .

 

 

Scenario----Here a Unique Batch no is created for every Process order .

 

(example:  Process order # 100001...5 qty....Batch no B1:....&.Process order # 100002...1 qty....Batch no B2:.....&.Process order # 100003...8 qty....Batch no B3:.....)

 

Process order sequenece

(1)First Process order for the First batch of a  Material -----------Inprocess Quality control is mandatory for Process order

(2)2nd  Process order for the second batch of a metarial to 11th process order for the 11th  batch of material in process -------QC not required.


(3)12th Process order for the12th Batch of Material ,------- Inprocess Quality control is mandatory for Process order

(4) 13th Process order to 22nd Process order (and its resp Batches),-------- in process -QC not required

(5) 23rd  Proces order will be the Last batch of this sequence--------------- for which QC run is mandatory. This Cycle closed


Next batch --(1) to (5) will repeat.

**********************************

 

QUESTION:???

How to control this sequence without much Z developments , keeping in mind there should be no scope for Manual errors.

 

 

THNX IN ADVANCE

HKR

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