100% Pass Quiz SAP - C_TS414_2023 Newest Latest Test Discount
100% Pass Quiz SAP - C_TS414_2023 Newest Latest Test Discount
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The aim of PDFTorrent is to support you in passing the SAP C_TS414_2023 certification exam. PDFTorrent present actual SAP C_TS414_2023 practice test questions for you. The world's skilled professionals share their best knowledge with PDFTorrent and create this set of actual SAP Certified Associate - SAP S/4HANA Cloud Private Edition, Quality Management C_TS414_2023
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SAP Certified Associate - SAP S/4HANA Cloud Private Edition, Quality Management Sample Questions (Q53-Q58):
NEW QUESTION # 53
What are some SAP recommended guiding principles to achieve clean core operations? Note: There are 3 correct answers to this question.
- A. Establish an organizational structure, technical foundation, and transformation methodology for clean core
- B. Establish regular housekeeping tasks and procedures
- C. Establish release management
- D. Define roles and responsibilities as part of a process transformation office
- E. Integrate clean core practices in the end-to-end value process chain
Answer: A,B,E
Explanation:
SAP's clean core principles (as per S/4HANA Cloud strategy) aim for a standardized, upgrade-friendly system:
* Establish an Organizational Structure, Technical Foundation, and Transformation Methodology for Clean Core (A): This foundational principle ensures governance and methodology (e.g., SAP Activate) for clean core adoption.
* Integrate Clean Core Practices in the End-to-End Value Process Chain (B): Embedding clean core into business processes ensures minimal customization and maximum standard use.
* Establish Regular Housekeeping Tasks and Procedures (C): Ongoing maintenance (e.g.,data cleanup) keeps the system lean and standard-compliant.
* Establish Release Management (D): While important, it's a broader IT practice, not a core clean core principle.
* Define Roles and Responsibilities as Part of a Process Transformation Office (E): Useful but not a primary SAP-defined clean core principle.
Thus, "A, B, C" are the correct answers.References: SAP Help Portal - "Clean Core Strategy"; SAP S
/4HANA Cloud Best Practices - "Clean Core".
NEW QUESTION # 54
During the production inspection, which elements does the system use to determine the layout of defects recording? Note: There are 3 correct answers to this question.
- A. Report type
- B. Confirmation profile
- C. Partner profile
- D. Status profile
- E. Catalog profile
Answer: A,B,E
Explanation:
Defects recording in SAP QM (e.g., transaction QE51N) during production inspections uses specific elements to define its layout and behavior:
* Report Type (A): Defined in Customizing (SPRO > QM > Quality Inspection > Defects Recording > Define Report Types), the report type determines the structure and fields available for defect entry (e.g., simplified or detailed layout).
* Confirmation Profile (C): This governs how defects are confirmed or structured during recording, especially in production-integrated scenarios (e.g., operation confirmation), influencing the defect entry screen.
* Catalog Profile (D): Assigned to the material or inspection type, the catalog profile (transaction QPCD) specifies the code groups and codes available for defect classification, shaping the recording layout.
* Partner Profile (B): Used in EDI or external integrations, not for defect recording layout in QM.
* Status Profile (E): Manages statuses (e.g., of notifications), not the defect recording interface.
Thus, "Report type," "Confirmation profile," and "Catalog profile" are the correct answers.References: SAP Help Portal - "Defects Recording in QM"; SAP S/4HANA QM User Guide - "Inspection Results".
NEW QUESTION # 55
A quality info record is released for the purchase of a material from a supplier. In what ways can you restrict the release? Note: There are 2 correct answers to this question.
- A. Until the supplier quality score is better than a threshold, by entering the minimum threshold
- B. To a quantity, by entering a release quantity
- C. Until the supplier has provided a quality certificate, by entering a certificate type
- D. To a period of time, by supplying a release date
Answer: B,C
Explanation:
The quality info record: Procurement (transaction QI01/QI02) manages supplier-material relationships and can impose release restrictions:
* To a Quantity, by Entering a Release Quantity (A): In the quality info record, you can set a "Release Quantity" field to limit the approved purchase quantity (e.g., 100 units). Once exceeded, further approval is needed, a standard feature.
* Until the Supplier Has Provided a Quality Certificate, by Entering a Certificate Type (B): You can specify a certificate type (e.g., "ISO 9001") in the "Certificate" field, blocking release until the supplier provides it, verified during goods receipt.
* To a Period of Time, by Supplying a Release Date (C): While validity dates exist, they define the record's lifespan, not a specific release restriction mechanism.
* Until the Supplier Quality Score is Better Than a Threshold (D): Quality scores influence supplier evaluation but aren't directly set as a release condition in the info record.
Thus, "A" and "B" are the correct answers, reflecting standard SAP QM functionality.References: SAP Help Portal - "Quality Info Record: Procurement"; SAP S/4HANA QM User Guide - "Supplier Release".
NEW QUESTION # 56
The receipt of a quality certificate should be recorded independently from the goods receipt. What is the necessary setting to fulfill this requirement?
- A. Assignment of a status profile in the certificate profiles
- B. Assignment of a status profile in the certificate type
- C. Indicator for enhanced certificate processing in the certificate type
- D. Control of certificate receipt in the quality info record: Procurement
Answer: D
Explanation:
To record quality certificate receipt independently from goods receipt (GR) in SAP S/4HANA QM, the system must decouple these processes:
* Control of Certificate Receipt in the Quality Info Record: Procurement (B): In the quality info record (transaction QI01), the "Certificate Control" settings (e.g., "Certificate Required" and "Check at GR" unchecked) allow certificate receipt to be recorded separately (e.g., via transaction QC55) before or after GR. This is the standard setting to achieve independence, ensuring the GR posts to blocked stock or proceeds without certificate enforcement at that step (SPRO > QM > Quality Certificates > Procurement).
* Assignment of a Status Profile in the Certificate Profiles (A): Certificate profiles (transaction QC01) define outgoing certificates, not incoming certificate receipt processes.
* Indicator for Enhanced Certificate Processing in the Certificate Type (C): The certificate type (SPRO > QM > Quality Certificates > Define Certificate Types) has an "Enhanced Processing" indicator, but it relates to certificate creation, not independent receipt recording.
* Assignment of a Status Profile in the Certificate Type (D): Status profiles in certificate types manage certificate statuses, not GR independence.
Thus, "Control of certificate receipt in the quality info record: Procurement" is the correct answer.References:
SAP Help Portal - "Certificate Receipt in Procurement"; SAP S/4HANA QM Customizing Guide - "Quality Certificates".
NEW QUESTION # 57
When you post a good receipt, where does the system check the current inspection stage for a material/vendor combination for upcoming inspection .
- A. Inspection Plan
- B. Quality level
- C. Characteristic
- D. Sampling scheme
Answer: B
NEW QUESTION # 58
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