Corrective Action for Deviation (delay) in the Delivery Schedule

B

bhavya vee

#1
Dear all,

Here is a case of Project Schedule variation, where in which the delivery date for the project is exceeded but still the project execution is in progress and during the data analysis we found the issue.
Kindly suggest me a right process that when the actions to be taken for the deviation in the delivery schedule? immediately after finding it or after the completion of the project?

Thanks in advance
Bhavya
 
Elsmar Forum Sponsor
S

ssz102

#2
Re: Corrective action

of cause, take corrective actions to meet the SPEC during this defective to be found
after the project completion, need to summary lessons learned and how to improve these shortage found
 

harry

Trusted Information Resource
#3
.................... Kindly suggest me a right process that when the actions to be taken for the deviation in the delivery schedule? immediately after finding it or after the completion of the project? ................
My answer is neither. Generally, projects should be monitored, evaluated and reviewed on a regular basis. You should take immediate action when signs indicate that you will not be able to complete the project in time with your resources in hand. You should avoid being literally caught with your pants down.
 
B

bhavya vee

#4
Dear Harry and ssz102,

Tank you for the information provided by you.:thanx:

Regards,
Bhavya
 
A

amit_rd

#5
I agree with Harry and want to add a few points:

1. Is this project done for fun? Or is there a customer involved?
2. Is there no impact on cost?
3. Are the team members involved in this project dedicated for this project only? Or this delay and their capacity requirements for its completion may impact some other projects?

Sorry for being brutal in asking these questions but - I sense a big gap in understanding here! You want to know when to initiate corrective actions, where as you first need to do correction.

The project tracking in terms of time, quality and cost is crucial and should be done at phases as planned during the frame scheduling.

My last question - Is there a frame schedule with defined intervals of monitoring? If not - establish it immediately for the pending project else you will loose the control over the project again.
 
B

bhavya vee

#6
Amit,

Thank you for your reply

In case of the delivery delay is due to customer like in which
a) raw material supply delay
b) prototype approval

Regards,
Bhavya
 

somashekar

Leader
Admin
#7
Here is a case of Project Schedule variation, where in which the delivery date for the project is exceeded but still the project execution is in progress and during the data analysis we found the issue.
You mean that during the project monitoring and review on a regular basis, you found the possibility of delay in completion ?
immediately after finding it or after the completion of the project?
Immediately and inform the concerned office also that a delay is foreseen.
On some projects you may be up with penalty for actual delay. Hence an immediate CA must be taken to come on course or get approved a time extension.
 
B

bhavya vee

#9
Hello,

Mr. Hussain,

Yes in this case you must find the cause of the NC i.e, why the delay in conducting a Management Review and record the same.:)

Regards,
Bhavya
 
S

steve hussain

#10
I guess you will need to have time shedule as well as good coomunication with your customer so as to keep them informed at all time.
 
Thread starter Similar threads Forum Replies Date
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
P 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
S Corrective Action from Internal Audits not performed ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 24
J We don't have enough Corrective action entries AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 10
T Timely Closure and "Ongoing" Corrective Action Nonconformance and Corrective Action 20
P Examples of Nonconformance, Corrective Action Requests, and Root Cause Analysis Nonconformance and Corrective Action 2
S How to Politely Close out a Nuisance Customer Corrective Action? Nonconformance and Corrective Action 11

Similar threads

Top Bottom