/ SIEMENS OPCENTER 03

Opcenter Quality

Closed-loop quality management from planning and shop-floor inspection to nonconformance and continuous improvement.

With Siemens Opcenter Quality, connect product, process and supplier quality to manufacturing operations and manage control plans, SPC data and nonconformances with complete traceability.

Explore the product
Opcenter Quality
Siemens Expert Partner
/ WHY CLOSED-LOOP QUALITY?

Turn fragmented inspection records into a preventive, measurable quality system connected directly to manufacturing.

01

Disconnected quality plans

Design requirements and shop-floor inspection steps must remain within the same context.

02

Late detection of deviations

SPC violations and nonconformances must become visible before losses escalate.

03

Weak problem solving

Findings, root causes, actions and effectiveness checks must be traceable end to end.

Opcenter Quality
/ QMS AND SHOP-FLOOR QUALITYThe quality loop closes from control plan through measurement result to corrective action.
/ QMS AND SHOP-FLOOR QUALITY

Manage quality within the process,
not only at final inspection.

Opcenter Quality combines quality planning, inspection, SPC, nonconformance, corrective action and supplier quality on one QMS backbone.

PlanDefine controls at the source
InspectEvaluate results in real time
ImproveManage root cause and action
  • Control plansProduct and process requirements become executable inspection steps.
  • Real-time feedbackMeasurement and SPC results reach the operator at the point of decision.
  • Organisational learningNonconformance and action history is used to prevent recurring problems.
/ QUALITY LOOP

From requirement to action,
a traceable quality flow.

The quality plan is validated through shop-floor measurement; when a deviation occurs, problem-solving and corrective-action workflows are triggered.

01Requirement
02Control plan
03Inspection and SPC
04Action and evidence
CONTEXTDECISIONRESULT
/ CAPABILITIES

Every layer of quality
within one management system.

Product, process, supplier and shop-floor quality data are managed through common classifications and workflows.

01 / PLAN

Quality planning

Inspection characteristics and scope are defined.

02 / INSPECTION

Inspection management

Incoming, in-process and final inspections are executed digitally.

03 / SPC

Statistical process control

Trends and rule violations are monitored in real time.

04 / NCR

Nonconformance management

Findings, containment, assessment and disposition are recorded.

05 / CAPA

Problem solving

Root cause, action and effectiveness checks are managed.

06 / SUPPLIER

Supplier quality

Incoming quality, PPAP and supplier performance are monitored.

/ CLOSED LOOP

Do more than record deviations;
prevent recurrence.

When a measurement exceeds limits, controlled action begins in the context of the affected product, process and responsible teams.

01 / DETECT

Measurement and SPC

Deviation is identified immediately.

→
02 / CONTAIN

Product and process

The affected scope is isolated.

→
03 / RESOLVE

Root cause and action

Permanent corrective action is implemented.

→
04 / VERIFY

Effectiveness check

Results are monitored and standards updated.

/ IMPLEMENTATION APPROACH

From quality model to shop floor,
in six controlled steps.

  1. 01
    Map quality processes

    Current plans, records and decision flows are analysed.

  2. 02
    Build the data model

    Characteristics, codes, defect and action classes are standardised.

  3. 03
    Connect the control plan

    Inspection steps are linked to product and process structures.

  4. 04
    Implement shop-floor collection

    Devices, measurements and operator interfaces are integrated.

  5. 05
    Test deviation workflows

    NCR, quarantine, CAPA and approval scenarios are validated.

  6. 06
    Improve performance

    Scrap, rework and recurring-defect data are analysed.

/ APPLICATION AREAS

Closed-loop quality
throughout the product lifecycle.

01

Manufacturing quality

In-process inspection, SPC and final inspection.

02

Supplier quality

Incoming inspection, PPAP and performance management.

03

Laboratory

Samples, tests, results and usage decisions.

04

Audit and compliance

Audits, actions, trails and regulatory records.

/ LET’S DEFINE THE NEXT STEP

Let’s assess MES/MOM fit
for your production operation.

We will review your current systems, priority use cases and integration needs with the relevant engineering team.

Request an MES fit assessment Your request is routed directly to the relevant engineering team.