Initiating Cultural Change in a Small Manufacturing Company

T

tekno9000

I am looking for ideas to initiate cultural change in a small manufacturing company. I want to create awareness about long term strategic planning, safety and doing things right first time. The catch is that I am not designated change manager, but I can influence changes indirectly with help of other managers who understand my motive. This is a privately owned company where owners and supervisors are more reluctant to change than the employees. For most change programs, the top management buy-in is a must but in my case the change is to be initiated and managed from the middle of the organization structure.

Please share your thoughts and experiences.

Thanks
 

Golfman25

Trusted Information Resource
Unless and until you get your "private owners" to change and embrace long term strategic planning, safety and doing things right first time you are wasting your time. You will only get frustrated. You'll be able to affect only what you control and nothing else. Your owners need to act like owners and drive (or at least accept) the change. Unfortunately I have been there and done that. What you do to change the owners will depend upon your relationship with them. Good luck.
 
D

DrM2u

I second Golfman's comment, based on my experience. In small companies change has to come from top down. The owners have to lead by example and drive the changes in culture, processes, methods and personnel to achieve what they want for their companies. I suggest you get their full commitment, support and buy-in if you want to drive anything company-wide.
 
Q

QCAce

I am looking for ideas to initiate cultural change in a small manufacturing company. I want to create awareness about long term strategic planning, safety and doing things right first time. The catch is that I am not designated change manager, but I can influence changes indirectly with help of other managers who understand my motive. This is a privately owned company where owners and supervisors are more reluctant to change than the employees. For most change programs, the top management buy-in is a must but in my case the change is to be initiated and managed from the middle of the organization structure.

Please share your thoughts and experiences.

Thanks

I've worked for the big corps and now I work for a small/medium privately owned company and I would agree with your assessment that you CAN change the culture from the middle. Many times I think we as quality professionals will mistake a lack of knowledge or understanding of quality systems by top management as a lack of management support. But I have yet to meet a top manager that did not want to see continual improvement, so as far as suggestions or ideas I think that is where you start:

1) Check -- as the managers you work with, "so what would your process look like if everything ran perfectly?" Then you can help them collect some data every time something wrong occurs. This can become a metric, (# of occurences/nonconformances per month, etc.) and a Pareto of the top issues each week/month.

2) Act -- use the data to help guide in writing corrective action(s) on the top issues.

3) Plan -- what work instructions or system changes could be developed/implemented to help prevent the issues from re-occuring.

4) Do -- self explanatory.

Then repeat the cycle of course. It's not hard. We make it harder than it needs to be. But if you can begin implementing this cycle with each of your department managers I believe you'll begin to change the culture.
 
T

tamale

Hey Tekno, show them the money.

If you are not the designated change manager you will most likely lack in credibility, so take another route. Show them the money.

It was one of the corner stones in Philip Crosby's philosophy.

Upper management reacts to losses and ways to recuperate them. So always cost your suggestions for improvement in terms of how much you can save in doing things differently.

Money talks and when it does, management listens.

Tamale :2cents:
 
Thread starter Similar threads Forum Replies Date
F ISO 14971:2012 - 4.3 Initiating Events and Circumstances ISO 14971 - Medical Device Risk Management 4
T Pilot's Checklist for Six Sigma - Steps to Consider when Initiating Projects Six Sigma 3
M Quality Week Ideas - Initiating a 'Quality Week' at our company Quality Tools, Improvement and Analysis 7
C Cultural and Communication Barriers between foreign workers as well as management. Philosophy, Gurus, Innovation and Evolution 6
D Definition What does cultural compatibility mean? Definitions, Acronyms, Abbreviations and Interpretations Listed Alphabetically 9
1 Developing Chinese Suppliers including Cultural and Language Issues Supplier Quality Assurance and other Supplier Issues 13
B Cultural Adaptation of Manuals Production Manuals and Work Instructions Document Control Systems, Procedures, Forms and Templates 4
kedarg6500 "Cultural compatibility" EFQM excellence model Various Other Specifications, Standards, and related Requirements 1
Sidney Vianna Cultural influence and "lineage" of Quality Systems Misc. Quality Assurance and Business Systems Related Topics 26
Q Various Excellence Models, Awards and ISO 9000 - Seeking Cultural Comparisons Misc. Quality Assurance and Business Systems Related Topics 9
S Change of ANDA ownership US Food and Drug Administration (FDA) 0
W Change predicate device CE Marking (Conformité Européene) / CB Scheme 1
P Production location change by supplier without info to customer Benchmarking 16
Sidney Vianna AS9100 News AS9101 Change Presentation Material AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 0
adztesla Design change and Process change Class 3 medical device Medical Device and FDA Regulations and Standards News 2
E Change in manufacturer address US Medical Device Regulations 2
adztesla Adding new supplier/ Medical device design change ISO 13485:2016 - Medical Device Quality Management Systems 2
adztesla Medical device Drawing related change justification Other Medical Device Related Standards 0
I Integrating CAPA and Change Control processes ISO 13485:2016 - Medical Device Quality Management Systems 3
J Raw Material Supplier Site Change US Food and Drug Administration (FDA) 0
W Notify FDA of Change of Ownership? US Food and Drug Administration (FDA) 2
D Implementation deadline - non significant change acc. to MDCG 2020-3 EU Medical Device Regulations 3
M IVD Device Design Change Medical Device and FDA Regulations and Standards News 2
D Little Help with "Tooling Change Program" for perishable tooling (8.5.1.6) IATF 16949 - Automotive Quality Systems Standard 4
C New 510(k) for non-patient contacting material change US Medical Device Regulations 2
T Minor Change vs. New Revision AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 4
Y Change in Legal Manufacturer US Medical Device Regulations 6
M If You Could Change One Thing... Misc. Quality Assurance and Business Systems Related Topics 12
Crimpshrine13 Bulk Process (Electroplating), Control Plan, and Process Change IATF 16949 - Automotive Quality Systems Standard 1
S Supplier change management Supplier Quality Assurance and other Supplier Issues 3
X IATF 16949 Section 3.2 Change of ownership IATF 16949 - Automotive Quality Systems Standard 2
adztesla Change in material vendor - Medical device ISO 13485:2016 - Medical Device Quality Management Systems 4
JoCam Change of Legal Manufacturer EU Medical Device Regulations 3
Sidney Vianna Informational ISO/TS 10020:2022 Quality management systems — Organizational change management — Processes Other ISO and International Standards and European Regulations 0
0 Complaints time series significant change Customer Complaints 41
N Malaysia Shelf Life Change Other Medical Device Regulations World-Wide 2
P Self Certified Class 1 MDR 2017/745 Design Change CE Marking (Conformité Européene) / CB Scheme 2
O Article 120 - significant change interpretation EU Medical Device Regulations 7
V Would the customer drawing change necessitate re-PPAP of the Product? APQP and PPAP 3
S Do we have to create a new PPAP to our customer if our Sub Contractor had to change? APQP and PPAP 10
M PMA submission change Medical Device and FDA Regulations and Standards News 0
U Change to the manufacturing Date for a device in the field US Medical Device Regulations 0
F Change in address for critical supplier - does NB need to be informed? CE Marking (Conformité Européene) / CB Scheme 20
K Change in address on ERLM US FDA: Implications to import US Medical Device Regulations 0
N Change our Registrar? Pros and Cons ? Registrars and Notified Bodies 8
F Using non-randomized clinical study for change in existing 510(k) device? US Food and Drug Administration (FDA) 1
FuzzyD ISO 13485 change in process ISO 13485:2016 - Medical Device Quality Management Systems 3
R IVD Label Change China Medical Device Regulations 1
Judy Abbott Change of PVC stabilizer Japan Medical Device Regulations 6
R IVD Label Change Requirements Other Medical Device Regulations World-Wide 0

Similar threads

Top Bottom