Corrective Action - Assigning KPIs to Non-Guilty Processes

Q

QAMTY

Hello all

How do you manage CA's assignement, like this:

In an external audit the delivery process resulted with on NC, because delivered product to client lately and didnt complied with goal.

Goal was set to max 5 late deliveries at month.
But this process complied very well, the problem was that previous process
who sent the product very late.

Who should resolve the nc ( surely an CA) the delivery process or the previous process? the NC was risen to Delivery.

Should the delivery process keep this KPI, because normally other processes are the cause of the late deliveries?

Thanks for your inputs
 

charanjit singh

Involved In Discussions
As for as the external auditor is concerned the non-conformity is against the Delivery Department. The cause of the NC however was the delay by the Production department. This is a common problem in many manufacturing organisations. Internally therefore KPIs for Production should include meeting the delivery commitment within the fixed target unless not included already.

Similarly the KPIs for the Delivery department should also include an upper limit (hours/days etc.) within which the shipment should actually be made once they receive the material from Production.

It will however be interesting to investigate and discover the root cause of delay and resolve the problem, because that is what resulted in the NC being raised in the first place.
 

charanjit singh

Involved In Discussions
I am sure you must be having an internal procedure/process for Corrective Actions. Usually this will involve a multi-function group. Responsibility for the NC, as far as the organisation is concerned, is not necessarily that of the department to whom it is issued. It is the result of investigation that will bring this out.

So the key is investigation and determination of what CA should be taken and take action as appropriate.
 

somashekar

Leader
Admin
Planning, Payments to suppliers, supply chain derailment, leadtime going out of control, production capacity ... several factors can be the reason. Do not target a process or person. Analyse and find out which is the weakest link in your chain, and work to build strength there.
 

howste

Thaumaturge
Trusted Information Resource
Who should resolve the nc ( surely an CA) the delivery process or the previous process? the NC was risen to Delivery.
It depends on what causes were determined. After the causes have been determined, people with the ability to eliminate the causes should take the actions. Then (ideally) someone who is independent of the actions should verify that the actions taken were effective in eliminating the causes and preventing recurrence.

Should the delivery process keep this KPI, because normally other processes are the cause of the late deliveries?
The KPI is relevant to multiple processes, so it can apply to all of them. In addition, as Charanjit Singh pointed out, you can have KPIs that are more specific to each process.

Production should be held accountable to a production schedule that will complete the product before it is due to ship. They could have a KPI for this. Delivery should be held accountable to ship product in a set amount of time. They could have a KPI for this. As Somashekar pointed out, Purchasing/Supply Chain should also be held accountable to get product to Production on time. They could have a KPI for this. Together, all processes are responsible for the overall KPI for on-time delivery.
 

Bev D

Heretical Statistician
Leader
Super Moderator
As Deming would remind us: it's a system. neither physics nor 'transactional' systems respect organization charts. the 'owner' should be the person who is responsible for investigating and implementing solutions for the problem. it doesn't mean they 'caused' the problem.
 
Thread starter Similar threads Forum Replies Date
T Corrective Action Risk Matrix AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 11
T Measuring Corrective Action Effectiveness AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 10
T Corrective Action vs. Countermeasure AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 6
L Globalization of corrective action and follow up IATF 16949 - Automotive Quality Systems Standard 17
H Can Non-conforming outputs & Non-conformity & Corrective Action procedures be merged Nonconformance and Corrective Action 8
M Root Cause and Corrective Action for CAPA's lacking validation/verification ISO 13485:2016 - Medical Device Quality Management Systems 19
H Ever given an Operations Manager an internal Corrective Action Request? Nonconformance and Corrective Action 5
B Human error corrective action 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 15
G Use of Supplier's Corrective Action Form vs. Corporate Form Supplier Quality Assurance and other Supplier Issues 4
M Corrective action for a defect from customer's mistaken Nonconformance and Corrective Action 1
Q Corrective action ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 17
H Streamlining audit response and corrective action processes ISO 13485:2016 - Medical Device Quality Management Systems 9
Q Corrective Action Notification - Registration Audit ISO 13485:2016 - Medical Device Quality Management Systems 12
S I need help in corrective action plan Nonconformance and Corrective Action 15
B NADCAP Rejection Response to Root Cause Analysis and Corrective Action. Nonconformance and Corrective Action 1
T Continual Improvement as Result of Corrective Action? Preventive Action and Continuous Improvement 32
3 Non-conformance Register vs Corrective Action Register ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 18
A Corrective Action Training ISO 13485:2016 - Medical Device Quality Management Systems 1
R Not every INCIDENT report will lead to a corrective action EU Medical Device Regulations 7
L Separate Corrective Action and Preventive Action Procedures ISO 13485:2016 - Medical Device Quality Management Systems 13
T AS9100D Clause 10.2.1g Supplier Corrective Action for each and every nonconformity? AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 3
R Non conformance (NC) or Corrective & Preventive action (CAPA) CE Marking (Conformité Européene) / CB Scheme 7
D Corrective Action Timing - IATF CB Deadline IATF 16949 - Automotive Quality Systems Standard 2
R AS 9100D - Containment and Corrective action AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 3
P Customer Corrective Action Requests in OASIS? AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 4
C Corrective action for failure in documents control ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 10
G Assignable cause/corrective action list for SPC Software Statistical Analysis Tools, Techniques and SPC 3
S Can we provide training plan as corrective action for IATF 16949 Non conformity? IATF 16949 - Automotive Quality Systems Standard 9
P Corrective Action Response for Missed bumps on brake press Manufacturing and Related Processes 2
B Stakeholder Initiated Corrective and Preventive Action Misc. Quality Assurance and Business Systems Related Topics 5
B Corrective and Preventive Action (CAPA) A Key Process of the Quality Management System Dec 17... Training - Internal, External, Online and Distance Learning 0
I When exactly can a corrective action be closed? Nonconformance and Corrective Action 3
L What to do if a Corrective Action requires several extensions Nonconformance and Corrective Action 7
qualprod Best criteria to measure Corrective Action effectiveness - Poor Maintenance ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 10
Ashok sunder Is it possible to reduce Risk likelihood and impact Post control Ranking after corrective action taken for risk? FMEA and Control Plans 1
E CAR (Corrective Action Report) with questionable Root Cause ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 16
B How to reply NCR on ineffectiveness of corrective action during IATF external audit? This is repeated issue whereby some mistake was done. IATF 16949 - Automotive Quality Systems Standard 7
I AS9100D Non-conformance for 10.2.1 b 2 and 10.2.1. b 3 e and f - Corrective Action AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 10
I Corrective Action Tracking for Product and Process in the same system? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 6
Ashok sunder Is it possible to reduce FMEA Occurrence and Detection Ranking after corrective action taken for customer complaints? FMEA and Control Plans 6
R CIP (Corrective Action) requirements - ISO 9001 clause 10.2 ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 10
E CAR (Corrective Action Request) Due Dates ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 17
E Corrective Action or Customer Complaint ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 16
J If Corrective and Preventive Action were truly Effective IATF 16949 - Automotive Quality Systems Standard 3
qualprod Is a Corrective Action Expected if a Quality Objective is not in compliance? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 38
M Corrective Action Effectiveness Nonconformance and Corrective Action 5
P Documentation for correction, corrective action, mini CAPA Nonconformance and Corrective Action 9
pziemlewicz Interesting Discussion Addressing Human Factors in Corrective Action AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 23
S Formal written response to a corrective action? Nonconformance and Corrective Action 9
Q AS9100D Corrective Action Procedure needed Document Control Systems, Procedures, Forms and Templates 1

Similar threads

Top Bottom