When do I need to calculate Process OEE?

Thread Attachment browser
R

ravit

Starting to get Involved
#1
#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
 
Paper to QMS ad
Elsmar Forum Sponsor
R

ravit

Starting to get Involved
#2
#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

somashekar

Staff member
Super Moderator
#3
#3
ravit said:
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
Click to expand...
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...
 
R

ravit

Starting to get Involved
#4
#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

somashekar

Staff member
Super Moderator
#6
#6
ravit said:
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
Click to expand...
Keep OEE aside for a while.
What do you need to do exactly for your process.
Reduce defects ?
Improve speed ?
any other .....
 
R

ravit

Starting to get Involved
#8
#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

somashekar

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

Ravi
Click to expand...
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.
 
You must log in or register to reply here.
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
SocalSurfer AS9100 new certificate, but need QMS software, help Quality Assurance and Compliance Software Tools and Solutions 2
A Demonstration of Equivalence - Need for comparing biological characteristics for an SamD EU Medical Device Regulations 1
G Need to change KPI we called NC parts (maximum 3%.) to FTQ (first time quality) IATF 16949 - Automotive Quality Systems Standard 4
W Need for current design or process control FMEA and Control Plans 2
L Turkish Requirements - Does the Software need to be translated? CE Marking (Conformité Européene) / CB Scheme 2
J Need for a cleanroom in the manufacture of a medical device for a clinical trial EU Medical Device Regulations 4
S Need help with analysing a survey on minitab Using Minitab Software 1
M IATF 16949 8.5.1.3 Verification of job set-ups - Do we need secondary check? IATF 16949 - Automotive Quality Systems Standard 7
P Electrosurgical Device User Need: Cord Flexibility -> Requirement Other Medical Device and Orthopedic Related Topics 4
P Do I need to get registered or have German entity to sell IVD products in Germany? CE Marking (Conformité Européene) / CB Scheme 2
J Documentation structure - Do I need Work Instructions? Document Control Systems, Procedures, Forms and Templates 23
G Need resources / tutorials about OPS (Operation) for ISO IT (Information Technology) Service Management 8
D Do non-IATF customers need to be included in audit scope? IATF 16949 - Automotive Quality Systems Standard 23
M Do you need an Applicable general safety and performance requirements Checklist? EU Medical Device Regulations 2
Y Does Solidworks (2D/3D drafting modules) need validation? Other Medical Device and Orthopedic Related Topics 5
M Do we need to create a new CER or can we just update the existing CER EU Medical Device Regulations 3
K A proposal for the model Quality Management - I need help for the project ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 2
B Record Management - Does the QMS need to control templates of records? Records and Data - Quality, Legal and Other Evidence 17
Q Need clarification on requirements.... Class i, gmp & 510(k) exempt Medical Device and FDA Regulations and Standards News 12
U Do we need clinical trial data for Class IIa medical device under MDR EU Medical Device Regulations 7
G Do we need to QA cert? We only plan to supply reagents Medical Device and FDA Regulations and Standards News 3
I MSA requirement for 5 Micrometers + CP changes need customer approval? IATF 16949 - Automotive Quality Systems Standard 2
R Evaluating the need for preventive action Preventive Action and Continuous Improvement 3
R Probability - Need a help to solve the below question Statistical Analysis Tools, Techniques and SPC 5
E In need of a new TGA sponsor - Small software company Other Medical Device Regulations World-Wide 4
8 Need Help - Runout - Function Gage Inspection, Prints (Drawings), Testing, Sampling and Related Topics 7
B Need For BIS Standard Mark? Imported OEM's Power supply,Li-Ion Battery Other Medical Device Regulations World-Wide 0
F How many signatures do we need on calibration certificates? ISO 17025 related Discussions 8
B We need a QMS: file-based templates or software Other Medical Device Related Standards 23
M AQL table - I need to sample 1250pcs AQL - Acceptable Quality Level 3
atitheya Need of conducting medical trials in European Union EU Medical Device Regulations 2
L Gage R&R studies for identical Devices - Need to confirm the requirement to perform them Reliability Analysis - Predictions, Testing and Standards 2
D Does every piece of equipment used in a laboratory need to have an IQ protocol written and executed? ISO 13485:2016 - Medical Device Quality Management Systems 1
I IATF16949 Audit Preparation, Need "searchable" ANPQP 3.1 or latest IATF 16949 - Automotive Quality Systems Standard 1
A Does Class 1 Medical Device need to be certified to MDSAP? Canada Medical Device Regulations 5
S New to FAIR, need help in filling it out AS9100, IAQG 9100, Nadcap and related Aerospace Standards and Requirements 8
S ISO 9001:2015 & ISO 14001:2015 - I need a format for Design & Development planning ISO 14001:2015 Specific Discussions 2
M Informational Some things the EU MDR 2017/745 does not tell you, but you may need to know to comply with it effectively – Part 1 Medical Device and FDA Regulations and Standards News 0
S NADCAP approval for Conventional Machining and Chemical processes - need assistance AS9100, IAQG 9100, Nadcap and related Aerospace Standards and Requirements 10
S Do we need to validate Software used in Drug discovery and development process? Qualification and Validation (including 21 CFR Part 11) 2
W Tying the need for Demand Planning to a section of AS9100/9110 AS9100, IAQG 9100, Nadcap and related Aerospace Standards and Requirements 4
R Do we need to treat local law as external origin documents? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 15
S Need Assistance in Visual Inspection - Tiny electronic components AS9100, IAQG 9100, Nadcap and related Aerospace Standards and Requirements 11
D Do we need normal data for gage r&r studies? Gage R&R (GR&R) and MSA (Measurement Systems Analysis) 5
Similar threads
Top Bottom