DoeRun SitewLoc Sw40k Report
DoeRun SitewLoc Sw40k Report
TABLE OF CONTENTS
Report Sections: Appendices:
1. Executive Summary 4. Audit Plan Assessment Summary Matrix
2. Auditor Commentary 5. Audit Records Process Summary
3. Auditee Information 6. Report Distribution Corrective Actions List
Opportunities for Improvement
Best Practices Observed
An audit was conducted at the location(s) on the date(s) cited above. The purpose of
this audit was to ensure that the auditee was continuing to maintain a documented and
effective Quality Management System, to meet the organization’s objectives, in
conformance with the Quality Management System requirements. A draft audit report,
consisting of the audit team recommendation (R20.36) and related corrective action
notifications (R20.35), was provided to the organization by the Lead Auditor prior to the
closing meeting.
The audit followed SRI's guidelines and procedures. The scope of the audit was a
review of the scheduled processes and any area(s) of nonconformance cited and/or
remaining open from the previous audit. In preparation for the renewal audit, planning
considered the performance of the Management System over the period of certification
and included a review of the previous surveillance audit reports.
Timing requirements for responding to Corrective Action Notifications are listed on the
second page of the R20.35 form, which is part of the draft audit report.
The recommendation in the draft audit report is any one of the following:
• Audit results observed were better than the previous audit activity.
• CAAT auditing techniques (of any type) were used during this event: No.
• The audit objectives have been fulfilled, and any applicable CAAT methods were
effective in fulfilling audit objectives.
The audit evidence collected during an audit will inevitably be only a sample of the
information available, partly due to the fact that the audit is conducted during a limited
period of time and with limited resources. Therefore, there is an element of uncertainty
inherent in all audits, and all users of the results of the audit should be aware of this
uncertainty.
The audit team would like to thank all personnel for their hospitality and cooperation
during the audit.
Based on the audit investigations, interviews, observations, and review of records, the
following comments summarize the audit team’s observations and findings:
Internal Audit Results: The Internal Audit activities associated with the
company's QMS were reviewed for this audit and were
found to follow an established and documented process.
(Internal Audit Policy PCP-471-006, Internal Audit
Planning & execution PCP-PCP-471-007), The
company audit schedule and related audit records were
reviewed for the audit. The schedule revealed that
internal audits of the QMS are conducted 2 times per
year for each key process. (See OFI-3) The records
reviewed indicated that all key process were audited in
2023. There were no NCs written on these audits in
2023.
Notable changes Employee count total is now 331 (from 327). There were
(e.g., address, management no other changes at this time.
rep., shifts, scope,
processes, employee count,
etc.):
Corp Office: 1801 Park 270 Drive, Suite 300, St. Louis, MO 63146 Auditee No: 0179-00
881 Main Street, Herculaneum, MO 63048 Auditee No: 0179-01
18594 Highway KK, Boss, MO 65440 Auditee No: 0179-02
Auditee Contacts
Mr. Grant DeShon, Quality Engineer
The Doe Run Company - Metals Division
1801 Park 270 Drive, Suite 300, St. Louis, MO 63146
Tel: 573-538-2706
Email: [email protected]
Audit Event
Renewal: 03/11/2024 - 03/15/2024 Total Mandays: 5.5 (on-site)
John Griffin, Lead Auditor
Audit Scope
Standard: ISO 9001:2015 (non-design)
Areas Identified As Not Applicable: 8.3 Design and development of products and services,
8.5 Service Provision (Only), 8.5.1.f Validation and Revalidation of Special Processes, 8.5.3
Property belonging to customers or external providers
Scope: Production of high quality lead, lead alloys, and propylene chips.
SIC Codes: 3341
IAF: 17
NACE Codes: DJ27.4
No. of Employees: 331 Total
Products: Lead Products
Regulatory/Statutory Requirements: Radioactive Materials; Conflict Minerals; NAFTA
Accreditation Mark(s): ANAB, RvA
Registration Approach: Site with location(s)
Certificate Expiration: 04/27/2024
No Shifts: 4
Times of Shifts: 4 crews-A, B, C, D, 5:00am-5:00pm and 5:00pm-5:00am
The audit plan, audit team members, and qualifications, representatives, working documents,
audit plan schedule, process matrix, and auditor assignments have been reviewed with the
organizations and are on file with SRI. The final Audit Plan is considered part of the report and
is maintained as an audit record.
Audit Records
Form R20.36: Which shows the registrar confirmation of the audit results was completed,
signed by both parties on-site, returned to SRI, and is on file.
Assessment Narrative: The pre-audit/post audit conference list of attendees and standard
agenda are on file, as is the agenda. The registered company has acknowledged and signed
any corrective action notifications issued at this event.
The SRI Auditor Notes: Auditor notes were captured and returned to SRI, along with the
“Interview Listing” (I8-3), all of which are on file.
Assessment Summary Matrix: The assessment summary matrix was completed by the lead
assessor and indicates the areas in which the selected processes were assessed and the areas
requiring corrective action. If there are several distinct audit tracks or business units, each has
a matrix completed for it. The matrix is provided.
Corrective Actions: If any, are included with this report and summarized in numerical order,
showing the referenced cited standard section, process, a description of the nonconformity, and
the level of severity indicated as "M = Minor" or "H = Hold.” Form R20.35 provides the detailed
nature of the nonconformance.
Opportunities for Improvement: If the lead auditor noted opportunities for improvement (OFIs),
these were provided to the auditee during the post-audit meeting. The opportunities for
improvement are listed.
Report Distribution
Distribution by SRI is only to the auditee, the auditor assigned for the next scheduled audit
event, SRI, and any accreditation body, when requested, where their oversight is required.
Performance
Customer Service X
Lab X
Logistics X
Maintenance X
Management X
Poly Chip X
Quality Services X
Refinery X
Sales / Purchasing X
Shipping X
Traffic X
Process Comments
Customer Service The Customer Service activities associated with the company's
QMS were reviewed for this audit and were found to follow an
established process. The process for customer service and
meeting customer requirements is managed through the
Corporate Sales group located in St Louis, Missouri. This
group is in contact with Outside Sales who are in direct contact
with the company's customers. Feedback from the customer
concerning pricing, delivery, and quality, are forwarded to the
Boss, Missouri Quality Manager to be addressed in the
company QMS/CAPA process.
Lab The Lab activities associated with the company's QMS were
reviewed for this audit and were found to follow an established
and documented process. The lab activities are primarily to
provide test data to the refining process as to the condition of
the Lead alloys as they are being adjusted with the proper
amounts of trace elements, and to verify that the products are
at or below maximum levels of trace elements per customer
specifications. Testing also confirms that the final product
meets the spec requirements of the customer. A spectrometer
is used to check elements in the beginning, middle, and final
stages of the adjustments to the elements "assays" to meet
customer requirements. The data from each spectrometer test
is saved in hard and electronic forms and is stored for life.
Upon final spectrometer testing, the data is transferred using
the AS400 system to a certificate of analysis (COA) form to be
sent with the materials to the customer. The spectrometer
operator was very senior and had been with the company for
over 30 years. Operators interviewed during this part of the
audit were extremely competent and aware of the QMS and
their contributions to it.
Quality Services The Quality Services activities associated with the company's
QMS were reviewed for this audit and were found to follow an
established and documented process. These series of
processes serve to support the main QMS function which is to
recycle and reuse lead materials. The support areas such as
management review, internal audits, corrective actions, and
customer satisfaction were reviewed during the audit with
results described in other areas of this audit report.
6.0 Risk analysis for the QMS was managed through the
management review activity. See (OFI-1), QMS goals and
objectives were reviewed and were found to be managed.
QMS objectives were reviewed for the audit and is covered in
other areas of this report (Management review). (See OFI-2)
Poly Chip The Poly chip production activities associated with the
company's QMS were reviewed for this audit and were found
to follow an established and documented process. (QAM
Process flowchart pg. 6, Buick resource recycling facility
management system handbook section 3) The Poly chip
production activities associated with the company's QMS (or
BSN) were reviewed for this audit and were found to follow an
established and documented process. This process takes used
batteries and crushes them, separating the lead content from
the casing, collecting the acids and neutralizing them and
processing it to later be treated. The process feeds the battery
stock into series of crushers, the material is put on belts that
separate the lead and plastic. The plastic is blown into trailers
where it is transported to recyclers. The lead is moved to the
reverb and blast furnaces to be refined.
File ID: DoeRun_SitewLoc_sw40k_report Page: 14
Process Comments
(Continued) The crushing process is fully automated; operators observe the
materials moving on belts and check for mixed material
streams. The electronic process control panel shows the
system in use in real time allowing operators to monitor the
material flows, amperages of the motors and other operational
parameters. Adjustments to the process can be made in real
time if non-conforming conditions are found. The operator was
observed and operators interviewed during the audit. Evidence
showed the operators, when interviewed, were competent,
highly skilled and very senior. They were aware of their QMS
and their role in it.
The following Opportunities for Improvement were identified during this audit activity:
Process Description
Quality services OFI-1,3,4,6 The company could consider creating and expanding KPIs
for such support areas as Maintenance (unscheduled downtime) Sales
(% lost sales), Purchasing (Supplier performance YOY) and Shipping
(on time delivery) that encourage continuous improvement.
Management OFI-2 The company could use a SWOT analysis or a similar document
to record and identify risk issues for the purpose of creating risk
mitigation activities that are proactive.
The following Best Practices Observed were identified during this audit activity:
Process Description
Lab BP-1 The customer makes and keeps all production data including
all spectrometer test data in both hard and electronic copy form for
reference as quality record for life.