Supplier Quality Program Information Worksheet Rev 0.pdf

PDF 393 KB Posted

Attached to
B212 and LS212 D&D Planning Sources Sought Federal contract opportunity
Solicitation number
B667987
Issued by
Department of Energy

About this file

This is a Supplier Quality Program Information Worksheet from Lawrence Livermore National Laboratory (LLNL) designed to assess potential suppliers' quality management systems and capabilities. The form requires detailed information about the supplier's quality certifications (including AS9100D, ISO 9001:2015, ISO 17025:2017, and NQA-1-2018), quality management processes, and inspection procedures.

The worksheet contains specific questions about the supplier's quality organization, document control processes, nonconforming items handling, equipment calibration, counterfeit item prevention, personnel training, supplier selection and monitoring, and corrective action procedures. The form includes spaces for indicating various types of inspection performed (incoming, in-process, final, and audit) and requires documentation supporting all quality processes. The completed form may be shared with the Department of Energy (DOE), National Nuclear Security Administration (NNSA), and other DOE/NNSA operating subcontractors.

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Text version

Supplier Quality Program Survey, Rev. 00

Supplier Quality Program Information Worksheet

SUPPLIER INFORMATION

Company Name:

Address:

City: State: Country (if outside USA):

Name & Title of person completing this assessment:

Phone: Email:

BUSINESS INFORMATION

Primary Product(s)/Services(s):

Are there multiple business locations? Yes No If yes, please indicate the following: same as above Headquarters Name:

Headquarters City: State: Country:

QUALITY MANAGEMENT SYSTEM REGISTRATIONS/CERTIFICATIONS

• Attach a current copy of the certificate for each registered standard

• If compliance is indicated (without registration), attach documentation supporting compliance (e.g., policy, quality manual, etc.)

AS9100D

Registered Compliant ISO 9001:2015 Registered Compliant

ISO 17025:2017 Registered Compliant NQA-1-2018 with NQA-1a-2009 with addendum Registered Compliant Other (please list): Registered Compliant Other (please list): Registered Compliant

Yes No

1. Is there an independent quality organization or job roles for quality management/assurance?

If Yes, please provide your organization's document title and revision. If No, please explain:

Yes No

2. Does your organization have a process for control of documents and records?

If Yes, please provide your organization's document title and revision. If No, please explain:

Yes No

3. Does your organization have a process for control, identification and segregation of nonconforming items until disposition by a competent authority has been completed?

If Yes, please provide your organization's document title and revision. If No, please explain:

Yes No

5. Does your organization have a process for detecting, preventing, and addressing counterfeit items?If Yes, please provide your organization's document title and revision. If No, please explain:

Yes No

6. Does your organization have a process to ensure your organization's personnel are trained, experienced, and qualified to perform work under the your organization’s quality system?

If Yes, please provide your organization's document title and revision. If No, please explain:

Yes No

N/A

4. Does your organization have a process to calibrate and maintain measuring and test equipment used for testing and inspection, as appropriate?

If Yes, please provide your organization's document title and revision. If No or N/A, please explain:

Supplier Quality Program Information Worksheet Rev. 00

Supplier Quality Program Information Worksheet

Yes No

Yes No

Date:

Signature (person completing worksheet)

This report may be shared with the Dept. of Energy (DOE), National Nuclear Security Administration (NNSA), and with other DOE/NNSA operating subcontractors.

For LLNL Internal Use Only Reviewed by: Date:

10. Check all types of inspection performed in this facility:

INCOMING IN-PROCESS FINAL AUDIT

Yes No

YeYess NoNo

9. When requested, is there a process to investigate and resolve rejected products and/or services found by the customer and implement corrective action to prevent future re-occurrence?

If Yes, please provide your organization's document title and revision. If No, please explain:

7. Does your organization have a process for selection and approval of suppliers and vendors to ensure they satisfy obligations and provide quality products and services?

If Yes, please provide your organization's document title and revision. If No, please explain:

8. Does your organization conduct evaluations (e.g., audits, review of test results, etc.) or ongoing monitoring of suppliers and vendors?

If Yes, please provide your organization's document title and revision. If No, please explain:

Company Name:
Address:
City:
State:
Country if outside USA:
Name Title of person completing this assessment:
Phone:
Email:
Headquarters Name:
Headquarters City:
State_2:
Country:
Date:
Primary Products/Servicess:
If yes, please indicate the following: Off
No: Off
Yes: Off
Compliant: Off
Registered: Off
Other (please list): Off
NQA-1-2018 with NQA-1a-2009 with addendum: Off
NQA-1-2017: Off
ISO9001-2015: Off
AS9100D: Off
If Yes, please provide a brief description:
If No, please explain:
If Yes, please provide your organization's document (or process) title and revision:
If No or N/A please explain::
If No or N/A, please explain::
If No, please explain::
If No, please explain:
Incoming: Off
Yes_1: Off
No_1: Off
Yes_2: Off
No_2: Off
Yes_3: Off
No_3: Off
Yes_4: Off
No_4: Off
N/A_4: Off
Yes_5: Off
No_5: Off
Yes_6: Off
No_6: Off
Yes_8: Off
No_8: Off
Yes_9: Off
No_9: Off
Yes_10: Off
No_10: Off
In-Process: Off
Final: Off
Audit: Off

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