Urgent opening for the position of QA/QC Engineer in Pharma machine manufacturing company at Ahmedabad (Santej)

QA/ QC Engineer

1 Nos.
87636
Full Time
4.0 Year(s) To 5.0 Year(s)
Not Disclosed by Recruiter
Production / Quality / Maintenance
Industrial Products/Equipment/Machinery/Projects & Engg
B.Tech/B.E. - Electrical; B.Tech/B.E. - Instrumentation
Job Description:

Job Description of Executive Engineer -QA/QC
1. Review of Technical documentation received from customer against all the
purchase orders /work orders.
2. Prepare QAP/Checklist for each equipment’s and handover to Production
for manufacturing process.
3. Inward inspection of all the items received from supplier for Bought out
Raw Material/components/machining items/Labor work etc.
4. Review of all Reports/Certificates as received from supplier and match the
same as per Design specification.
5. Raw material Check testing at NABL approved lab to be carried out as per
defined procedure.
6. Clearance of Inward items in the ERP system based on satisfactory
inspection against predefined specification.
7. Coordination with Purchase team for the improvement of Quality of
product and arrange vendor evaluation for new supplier.
8. Outsourcing inspection of critical items at supplier end regarding Final
drawing attached in the system.
9. Based on available data in the ERP system, prepare rejection analysis
Monthly and based on the same further action of Quality improvement to
be decided.
10. Coordination with interlinked department to improve the Quality of the
product.
11. Monitoring of manufacturing process and inspection as per QAP /ASME
/PED/IBR requirement and maintain the documentation.
12. Monitoring Welding /NDT activity at shop floor and review of Welding
documents & NDT documents.

13. Coordination with NDT service provider for the NDT related activity and
arrange visit as per shop floor requirement.
14. Coordination with TPI for stage wise inspection / Certification activity and
documentation signed off.
15. Final Inspection of equipment as per Approved documents of customer
(G.A. / P&ID / DR).
16. Final documentation preparation of all the equipment’s once the assembly
completed.
17. Maintain the quality of documentation in concern with Design/Automation
team.
18. Coordination with Sales team for the approval of FAT protocol from
customer.
19. Coordination with Service team for the approval of SAT/IQ/OQ protocol
from customer.
20. Preparation of WPS/PQR/WPQ as per ASME / PED requirement.
21. Inspection will be based on ASME/TEMA/PED/IBR requirement.
22. To calibrate the measuring instrument as per Master List at NABL approved
calibration Lab and update the Master as and when required.
23. Documentation Improvement to be done based on customer Feedback and
upgradation in Standard.
24. Follow ISO 9000 procedure related to the function.

For further description please call Megha on 9377677857 or you can mail your candidature on megha@postaresume.co.in

Company Profile

Pharmaceuticals Machine manufacturing Company since 50 years

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