SBS - The best value in QMS software

When do I need to calculate Process OEE?

ravit

Starting to get Involved
#1
HI,

I m calculating OEE for our process .

Is it consists of manual works also?
Because we are doing several processes manually.
Or we need to do calculation for only those process in which we are using machine?

Regards
Ravi
 
Elsmar Forum Sponsor

ravit

Starting to get Involved
#2
Distal PortionBalloon Assy. Manual OperationDistal PortionTip Welding Preparation Manual OperationDistal PortionTip Welding Distal PortionRX Preparation Manual OperationDistal PortionWelding ( two post ) Distal PortionFinal InspectionManual OperationBalloon AssySleeve Length cuttingManual OperationBalloon AssyFiber inspectionManual OperationBalloon AssyNotch cuttingManual OperationBalloon AssyProximal cutManual OperationBalloon AssyWelding PreparationManual Operation

These all are manual process, somewhere we are using two or more than two operators, in this case how to calculate OEE?

please help

regards
Ravi
 

somashekar

Staff member
Super Moderator
#3
HI,

I m calculating OEE for our process .

Is it consists of manual works also?
Because we are doing several processes manually.
Or we need to do calculation for only those process in which we are using machine?

Regards
Ravi
One of the E in the OEE is Equipment.
So its got to do with an equipment, manual or automatic or Numerically controlled.
So, If you have a foot operated press or a Toggle press, these equipments OEE can be calculated. How it effects your process is to be derived by you further...
 

ravit

Starting to get Involved
#4
hello sir,

Hope you are well.


For one single product , we have around 32 process. in most of them we have manual operations ( more that 50 % ).
At some process we are using two or more than two operators also.

How to proceed in this case?

Best Regards
Ravi
 

somashekar

Staff member
Super Moderator
#6
hello sir,

Hope you are well.


For one single product , we have around 32 process. in most of them we have manual operations ( more that 50 % ).
At some process we are using two or more than two operators also.

How to proceed in this case?

Best Regards
Ravi
Keep OEE aside for a while.
What do you need to do exactly for your process.
Reduce defects ?
Improve speed ?
any other .....
 

ravit

Starting to get Involved
#8
have you get my Excel sheet?

how to calculate it with several operators on single process?
or I need to calculate it only for those process on which we are using machines?

Regards
Ravi
 

somashekar

Staff member
Super Moderator
#9
Both, reduce defects and increase the productivity..

Ravi
Productivity improvement is called out everywhere.
When you reduce defects you increase productivity...
When you improve speed you increase productivity...
Where are you in productivity now and where do you want to touch to, and by when.
Have you done a Value Stream mapping.
What are your critical areas about Defect / Hold up ?
I did see the .xl sheet. Too much numbers, too little for me to make out.
 
Thread starter Similar threads Forum Replies Date
J Methods used to calculate Cpk value - Need help for Cpk Calculation Statistical Analysis Tools, Techniques and SPC 8
A Do we still need to Calculate Measurement Uncertainties (MU)? Measurement Uncertainty (MU) 6
X Calculating Tolerance with One Sided Limits - Need a Form to Calculate Statistical Analysis Tools, Techniques and SPC 6
N Effectiveness, miss rate and false alarm rate - Need formulas to calculate Gage R&R (GR&R) and MSA (Measurement Systems Analysis) 4
A What is the formula I need to calculate Pp and Ppk? Capability, Accuracy and Stability - Processes, Machines, etc. 26
S Cmk and Cpk - When will we need to calculate Cmk? Machine Capability Capability, Accuracy and Stability - Processes, Machines, etc. 4
briteme4 AS9102 First Article Inspection - do I need a second reviewer and signer? AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 2
J Furnace repaired - Do I need a new initial TUS? AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 1
B Does FDA Registration QSR need to cover non-medical devices for contract repackager? US Food and Drug Administration (FDA) 1
S Need ISO 15189:2012 Documentation toolkit. Document Control Systems, Procedures, Forms and Templates 0
J Need a contract monitoring Tool General Information Resources 0
P UDI-PI requirements on reusable surgical device, do we need serialisation? ISO 13485:2016 - Medical Device Quality Management Systems 3
J Need Help with FPY Data in Assembly Process Manufacturing and Related Processes 7
W 17025 and NIST handbook relationship (need advice) ISO 17025 related Discussions 8
lanley liao Does all of the suppliers need to integrated into the supplier list qualified of the company? Oil and Gas Industry Standards and Regulations 2
K Need procedure for D&D inputs? ISO 13485:2016 - Medical Device Quality Management Systems 4
S Need help on "Country of Origin" Medical Device and FDA Regulations and Standards News 0
Ed Panek Immediate need for 80601-2-56 Consulting expert. PM me for details Career and Occupation Discussions 0
Tagin You're Gonna Need a Bigger Root Cause Coffee Break and Water Cooler Discussions 12
M PSA Suppliers - CSR matrix and need the quality manual of PSA APQP and PPAP 6
M Need Help With Information Security Asset Risk Register IEC 27001 - Information Security Management Systems (ISMS) 2
K "World Class Product" based QM. I need advice. Quality Management System (QMS) Manuals 14
I Do I need to sign off my annual audit calendar? Internal Auditing 2
P Do we need to retrospectively use the "MD" symbol (indicating device is a medical device) on labels, e.g. finished devices within expiration date? EU Medical Device Regulations 2
M Do I need separation in my circuit with a medical charger? IEC 60601 - Medical Electrical Equipment Safety Standards Series 0
V Certified Auditor - Need of additional certification specific to industry ( GMPs) ASQ vs ECA vs others Professional Certifications and Degrees 1
D Low risk IVD study in the UK, do I need MHRA approval? UK Medical Device Regulations 1
A Medical Device Contract Manufacturer - Does the CM need to register with FDA? 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 3
J Records Control - Does each individual record need to be numbered? Records and Data - Quality, Legal and Other Evidence 2
N Is there a need for clinical test of Class IIa products (for MDR)? EU Medical Device Regulations 2
J Do Software Subcontractors need to be ISO13485 compliant in the EU? EU Medical Device Regulations 3
K Do I need a "State of the art" plan? CE Marking (Conformité Européene) / CB Scheme 1
S Need advice for schooling Quality Manager and Management Related Issues 5
R What information do i need to get from the device manufacturer 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 0
S Need guidance on project ISO 13485:2016 - Medical Device Quality Management Systems 2
H Need MSA 4th ed. compliant attribute MSA template General Measurement Device and Calibration Topics 4
J Need Change Control Yes/No Decision Tree Template ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 1
C Does an accessory need an IFU if it use is discussed in the Parent device IFU? 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 5
B Countries with no need for FSC (Free sales certificate) Other Medical Device Regulations World-Wide 0
R The term "Benefit Risk Ratio" in EU MDR, do I need to present benefit risk analysis as a RATIO Risk Management Principles and Generic Guidelines 4
A Brexit When does the UK responsible person need to be in place? UK Medical Device Regulations 10
R Do we need issue ECN (Engineering Change Notice) towards updated Material Specification? Design and Development of Products and Processes 2
N IPC-A-630 - Is this free or do i really need to pay for it? Manufacturing and Related Processes 4
C ISO/ IEC 17021 Resource requirement (need help) Document Control Systems, Procedures, Forms and Templates 5
P Need a programmer for QVI's VMS software for optical inspection machine Inspection, Prints (Drawings), Testing, Sampling and Related Topics 0
silentmonkey How to decide what characteristics need to be verified during incoming inspection? ISO 13485:2016 - Medical Device Quality Management Systems 5
D Change Approval Requirements - Does every change need formal customer approval? Design and Development of Products and Processes 17
T Do I need a qualified compiler for class B software? IEC 62304 - Medical Device Software Life Cycle Processes 3
E 13485:2016, Sections 4.1.6, 7.5.6 and 7.6 - Validation of Software - Need some Advice please ISO 13485:2016 - Medical Device Quality Management Systems 3
C ISO 13485 :2016 - CAPA - Does every CAPA need to be checked by regulations? ISO 13485:2016 - Medical Device Quality Management Systems 9

Similar threads

Top Bottom