SOP Readiness But
SOP Readiness But
S O P Readiness Guideline
Master
1K / 1A LVPT QC Approved HVPT SOP Ready
Schedule
Milestone OTOP @ 100% Q OTOP @ 100% Q OTOP, Q Approved OTOP, Q Approved HVPT OK
SPTT 3 SPTT 4
Tool Production Ready
SPTT SOP Readiness
QC Co check complete,
Check Sheet Check sheet
Quality Process Ready Approved for HVPT HVPT HVPT Complete
(ref SQAM) & Stress Test
Result
Production Process Ready
Should be completed already as Should be completed already Should be completed already Conduct activity and confirm
part of SPTT 3 before final HVPT with Capacity confirmed readiness items
PIC Timing
PC N-3 Step 1 - Calculate Vol per day base on lastest forcast
- Decide production pattern ( Lot/day, Lot/ week, Lot/Month)
PC N-3 Step 2 Input Production performance evaluation plan for N-2 month
PC N-3 Step 3 Confirm readiness activity e.g. Raw Mat't, Component, Manpower,. Etc.
PC N-2 Step 4 Confirm achievement of KPI & Target ( Initial Stock, Capability % OA)
Activity KPI
Supplier Production & Delivery Trial Problem Root Cause Countermeasure PIC Date
Part No Day : #1 #2 #3 #4 #5 #6 #7 #8 #9 #10 #11 #12 #13 #14 #15 #16 #17 #18 #19 #20 #21 #22 #23 #24 #25 #26 #27 #28 #29 #30 #31
Description Date : 1-Jul 2-Jul 3-Jul 4-Jul 5-Jul 6-Jul 7-Jul 8-Jul 9-Jul 10-Jul 11-Jul 12-Jul 13-Jul 14-Jul 15-Jul 16-Jul 17-Jul 18-Jul 19-Jul 20-Jul 21-Jul 22-Jul 23-Jul 24-Jul 25-Jul 26-Jul 27-Jul 28-Jul 29-Jul 30-Jul 31-Jul
Production Plan Supplier Daily Production Plan Daily Plan : 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 1 0
Actual Production Supplier Total Parts Produced OK + NG : 0
Actual Good Parts ① Supplier Total Parts produced Less Defects Total - NG : 0
Efficiency ② Supplier Actual Efficiency Target 95% 0% 0% 0% 0% 0% 0% 0% 0% 0% 0% 0% 0% 0% 0% 0% 0% 0% 0% 0% 0% 0% 0% 0% 0% 0% 0% 0% 0% 0% 0% 0%
Defect Ratio ③ Supplier Actual Good / Actual Prod'n Target Defect : 5% 0% 0% 0% 0% 0% 0% 0% 0% 0% 0% 0% 0% 0% 0% 0% 0% 0% 0% 0% 0% 0% 0% 0% 0% 0% 0% 0% 0% 0% 0% 0%
TBINA Delivery Plan TBINA Delivery schedule 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0
Actual Delivery Actual Delivery to STM / TBINA Actual Delivery : 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0
Stock in Store ④ Balance (Production - Delivery) Start Volume : 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0
Safety Stock (Pcs) Stock in Store / Average daily volume Target Days : 0.25 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0
Overall Judgement : ∆ ∆ ∆ ∆ ∆ ∆ ∆ ∆ ∆ ∆ ∆ ∆ ∆ ∆ ∆ ∆ ∆ ∆ ∆ ∆ ∆ ∆ ∆ ∆ ∆ ∆ ∆ ∆ ∆ ∆ ∆
Peak month Average daily volume Peak Volume is Oct 0 / TBINA working 22 days = 0 X = Did not achieve any target, D = Did not achieve daily production plan
X = Did
or NG
notratio,
achieve
Safety
anystock
target, D =isDid
level OK,not
O achieve
= Achieved
dailyallproduction plan
X = Did
or NG
notratio,
achieve
Safety
anystock
target, D =isDid
level OK,not
O achieve
= Achieved
dailyallproduction plan
X = Did
or NG
notratio,
achieve
Safety
anystock
target, D =isDid
level OK,not
O achieve
= Achieved
dailyallproduction plan or NG ratio, Safety stock level is OK, O = Achieved all
Supplier Production & Delivery Trial Problem Root Cause Countermeasure PIC Date
Part No Day : #1 #2 #3 #4 #5 #6 #7 #8 #9 #10 #11 #12 #13 #14 #15 #16 #17 #18 #19 #20 #21 #22 #23 #24 #25 #26 #27 #28 #29 #30 #31
Description Date : 1-Jul 2-Jul 3-Jul 4-Jul 5-Jul 6-Jul 7-Jul 8-Jul 9-Jul 10-Jul 11-Jul 12-Jul 13-Jul 14-Jul 15-Jul 16-Jul 17-Jul 18-Jul 19-Jul 20-Jul 21-Jul 22-Jul 23-Jul 24-Jul 25-Jul 26-Jul 27-Jul 28-Jul 29-Jul 30-Jul 31-Jul
Production Plan Supplier Daily Production Plan Daily Plan : 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 4 0
Actual Production Supplier Total Parts Produced OK + NG :
Actual Good Parts ① Supplier Total Parts produced Less Defects Total - NG :
Efficiency ② Supplier Actual Efficiency Target 95% 0% 0% 0% 0% 0% 0% 0% 0% 0% 0% 0% 0% 0% 0% 0% 0% 0% 0% 0% 0% 0% 0% 0% 0% 0% 0% 0% 0% 0% 0% 0%
Defect Ratio ③ Supplier Actual Good / Actual Prod'n Target Defect : 5% 0% 0% 0% 0% 0% 0% 0% 0% 0% 0% 0% 0% 0% 0% 0% 0% 0% 0% 0% 0% 0% 0% 0% 0% 0% 0% 0% 0% 0% 0% 0%
TBINA Delivery Plan TBINA Delivery schedule 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0
Actual Delivery Actual Delivery to STM / TBINA Actual Delivery : 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0
Stock in Store ④ Balance (Production - Delivery) Start Volume : 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0
Safety Stock (Pcs) Stock in Store / Average daily volume Target Days : 0.25 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0
Overall Judgement : ∆ ∆ ∆ ∆ ∆ ∆ ∆ ∆ ∆ ∆ ∆ ∆ ∆ ∆ ∆ ∆ ∆ ∆ ∆ ∆ ∆ ∆ ∆ ∆ ∆ ∆ ∆ ∆ ∆ ∆ ∆
Peak month Average daily volume Peak Volume is Oct 0 / TBINA working 22 days = 0 X = Did not achieve any target, D = Did not achieve daily production plan
X = Did
or NG
notratio,
achieve
Safety
anystock
target, D =isDid
level OK,not
O achieve
= Achieved
dailyallproduction plan
X = Did
or NG
notratio,
achieve
Safety
anystock
target, D =isDid
level OK,not
O achieve
= Achieved
dailyallproduction plan
X = Did
or NG
notratio,
achieve
Safety
anystock
target, D =isDid
level OK,not
O achieve
= Achieved
dailyallproduction plan or NG ratio, Safety stock level is OK, O = Achieved all
Factory Manager or above Page 1 of 1
Abnormal part handling confirmation sheet
Dear : TBINA Purchasing Engineering Division
From : ( Company name ) Mr.
We confirmed our Mass Production process as below items; Date :
Supplier confirmation
Process Flow Check items ( If no, please specify)
(Minimum requirement) Yes No
Concern item Countermeasure / Due date
Normal Production
Yes
OK Abnormal part
II 1) Clear WI/Std. of inspection to judge/verify Δ WI 560B sudah dibuatkan, Q-Point belum Dibuatkan Q-point 20/09/22
OK part confirming NG or suspect NG part
NG / Suspect NG
III -1) Red mark on "NG" point O
O NG sudah dimarking posisinya
2)Keep in red box
O Box NG sudah ada
NG part Suspect part 3) Record in NG record sheet Δ Area part yg suspect Ng ( Part ragu-ragu ) Dibuatin layout untuk tempat part suspect (need confirm GH) 20/09/22
-1) Mark on suspect NG point and/or tag info. Δ
2) Keep in suspect area
IV 1) Clear criteria to judge if it can be repaired Δ Q-Point belum dibuatkan Dibuatkan Q-point 20/09/22
OK Confirming 2) Clear Authorization for repair O PIC Produksi
OK part suspect part
NG V 1) Procedure to control repair part Δ Prosedur Repair belum ada secara Detail Dibuatkan Prosedur Repair 26/09/22
2) Keep part in separate area for repair O Laporan Sortir / Rework
O WI Repair sudah ada
3) Have repair WI
O Area Repair sudah ada khusus
Repair 4) Record in repair sheet & mark on part Δ penandaan part repair belum ada akan diatur di WI repair dan prosedur repair
5) Identify next process (for inspect) on tag
All ▽S or concern critical process items which can be inspected at final inspection/Quality Gate should be defined as inspection items. If
★ 1
there is and ▽S or concern critical processitems which can not be inspected directly, substitute items such as completed color mark which
previous production process assure sureness of▽S or concern critical processitems should be checked.
2
▽S mark is marked on ▽S inspection item in standardized work sheet.
Terdapat simbol delta S dan delta R pada WI
Inspection method to each inspection item and Q-Point should be clearly defined in standardized work sheet and every inspector can make a
★ 3 judgment of whether OK or NG without any difficulty.
Cleary procedure or standard when found ▽S or concern critical process defect<Repair,Re-check stock for> management level should
4 participated.
Necessary inspection time to each inspection item is clearly determined one by one in standardized work sheet and total inspection time is
★ 5 surely secured within takt time.
There is an instant feed back system to production process to review quality assurance level as soon as serious quality defect is detected by
inspector.(Incase of▽S or concern critical process problem, operator STOP,Call ,Wait and report to leader/supervisor immediately,
Leader/Supervisor communicate to production process in order to prevent reoccurrence and record.)
★ 7 มีระบบตอบกลับทันทีทันใดในกระบวนการผลิตเพื่อที่จะตรวจสอบ quality assurance level ทันทีที่เกิดข้อบกพร่องร้ายแรง ที่ตรวจพบโดย inspector (ใน
4M กรณีปัญหาของ ▽S or concern critical process พนักงานต้อง หยุด เรียก คอย และรายงาน leader หรือ supervisor ทันที leader/supervisor ต้องมีการ
แจ้งให้กระบวนการผลิตทราบ เพื่อป้องกันการเกิดซ้ำ และต้องมีการจดบันทึก )
Standardized work is being modified continually in order to level up defect detectability.(Ex.Improvement of difficult inspection job.)
Standardized work
8 Standardized work ต้องมีการปรับปรุงอย่างต่อเนื่อง เพื่อที่จะพัฒนาความสามารถในการตรวจจับชิ้นงานเสียของพนักงาน ( เช่น การพัฒนาการตรวจสอบ
ชิ้นงานที่ยากกว่าการตรวจสอบ )
Record Revisi SOP harus selalu update ( terdapat record revisi di WI )
Standardized work compliance of each inspector is being audited and coached for improvement by leader/supervisor periodically (At least 1
★ 9 time/week/inspector)
Inspector should be trained and qualified as planned.Only eligible inspector (Level 3 Up; Can do without any support) can conduct inspection
★ 10 job at final inspection/quality gate.
12
▽S sign mark is marked on inspection process for ▽S inspection process.
13
Daily preventive maintenance item of inspection machine/tool is clearly defined on check sheet.
Ⅲ Machine Terdapat C/S Mesin Daily
Daily Check up of inspection machine/tool is being conducted properly and regularly <both OK and NG condition by master sample>. Operator
14 check and fill in result on check sheet and approved by leader/supervisor.
15
Inspection table/surrounding should have good condition such as 4s /enough lux (lighting),noise
Before & After inspection,part must have clear identification and inspected part must be one piece flow
Ⅳ Material 18
C/S Incoming u/ Material + Label after cek
★ 19
Management confirm daily quality status at ASAKAI every day.(at least 1time/day)
Management follow up countermeasure progress of serious quality problem (ex. outflow defect to customer, serious defect detected by final
20 inspection.) at ASAKAI until 100% countermeasure completion and yokoten to similar part and process.
BIRA Sheet
Quality
Five-Why is being used seriously in order to find out real root cause for serious defect.
Management 21
A3 Report u/ Critical Problem (A3 Report Internal maupun external )
Supplier tier 2
Abnormal handling procedure is posted at the process or production line. Record of abnormality events should be kept and
Handling in abnormal 23 controlled.
condition