Ioc Api
Ioc Api
From: MR
29.06.2015
Opening meeting at 9:30am
1. Top Management
2. MR
3. Library
30.06.2015
1. MR continued from 29.06.2015
2. M&S(Post lunch session)
3. PPE Unit 2 & QA/QC-2
Production Planning Process
Production Process Record, Job Router, Work shop orders
issuance &
Control, Planning Production & Controls, Records Review
(Unit 2)
Manufacturing Process
Establishment of Process Control Documents, Product
Realization Documents, Product Quality Plans, Materials
technical Specifications
Validation of Process-API 6D Sec 1.4-NDE/HT/Welding &
coating
01.07.2015
1.
DD&D
API 6D & API 600 licensed products
Audit product questions Review
02. M&M including outsourced processes & verification of
purchased product ( Post Lunch Session)
03. Production Control Process(Machining)(Unit 2)
04. FF, NDE, HT
05. Welding
06. Assembly
07. QA(Inspection & Testing )(Unit 2)
02.07.2015
01. QA(Inspection & Testing)/Production Processes(Unit 2)
02. Identification & Traceability
03. Marking & API Monogram marking requirements
04. Control of NC product
05. IPI & Final Inspection(QA 2)
06. Standard room & Calibration(Post lunch session)
07. Customer Supplied Property(M&S)
08. Packing & Shipment
09. Preventive Maintenance(Unit 2)
03.07.2015
01. HR & Training
02. MOC(MR)
Closing Meeting at 5:00pm
Following are the minimum requirements for audit which need to be taken on
priority:
1. Document control: Make sure that no obsolete documents are
available/lying in your department & your area of working.
2. Quality Objectives: Updated quality objectives with all back up documents
should be available.
3. Identification & Traceability: All material/items/equipments should be
identified in all respective areas.
4. Inspection & Test Status: Inspection & test status of material is very
important & should be strictly as per Inspection & Test Status Plan.
5. Process Control: All machines should have process control cards properly
filled & endorsed by QC. Controlled drawings should be deployed on each
machine.
6. INC Records: Closed all INCs reviewed by MR should be available .
7. Non Conforming Area: Each machine shop, Assembly shop, testing shop
& inspection area should have earmarked area for non conforming
products.
8. Facility Tour: Auditor will take a round of entire facility on 29.06.2015 & will
select samples from shop floor from all areas including painting &
shipping. Hence all records & requirements should be completed &
records available.
9. Sample Cases: API 600 & 6D supply history has been circulated by M&S.
Auditor can select any random sample case for records verification for
audit.
10. House Keeping: Housekeeping should be given prime importance. Work
instructions in HINDI/PUNJABI duly controlled should be deployed at
respective machines/shops for operators reference.
Circulation:
1.
Mr. R.C. Chadha (GM)
2.
Mr Raj Kumar Gupta(Sr. Mgr QA-2)
3.
Mr. Manoj Kumar (QA Unit-2)
4. Mr. G D Sahni HOD (D,D&D)
5. Mr. Jogesh Saini HOD (M&S-LVL & LEX)
6. Mr. C.D. Duggal HOD ( MM Unit 1&II)
7. Mr. S.Ohri HOD (Export PPE)
8. Mr. Banwari Lal (PPE Unit-2)
9. Mr. Baljit QA (FF)
10.
Mr. Rohit (HRD)
11. Mr. Jai Kumar (HOD,FF)
12. Mr. Ashutosh Sharma(QA Unit 1)
13. Mr. Sanjeev Goswami(Shipping)
14. Mr. Suresh Kumar / Mr Gurvinder (MNM)
15. Mr. Charanjit Singh / Mr. Shkeel (MNE)
16. Mr Atul Khanna( Lab Unit I)
17. Mr Rajesh( Lab Unit II)
18. Mr Rajesh Virdi(Calibration)
19. Mr. Amit Kumar (Librarian )
20. Mr. Raj Kumar (NDT)
21. Mr. Jatinderpal Singh (QA IGR, Unit-1)
22.
Mr Maghir Chand(ASM Security)