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Supplier Quality Engineer (Medical Device Manufacturing/ East) job in Singapore at GMP TECHNOLOGIES (S) PTE LTD

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Supplier Quality Engineer (Medical Device Manufacturing/ East) at GMP TECHNOLOGIES (S) PTE LTD

Supplier Quality Engineer (Medical Device Manufacturing/ East)

GMP TECHNOLOGIES (S) PTE LTD Singapore Permanent
3,500 SGD - 5,500 SGD/Month
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Responsibilities:

  • Support Continuous Improvement projects that require basic Engineering and Project Management skills driven by process excellence thinking and actions throughout the organization.
  • Routinely work with suppliers, MDT sourcing and/or MDT procurement functions to define new opportunities and improve gaps in process performance.
  • Establish and successfully execute supplier management and development plans which will align to overall business objectives.
  • Developing continuous improvements and providing leadership for improving the supplier relationship.
  • Perform thorough supplier audits and assessments of their processes and QMS and drives improvement.
  • Perform routine MRB review and disposition of nonconforming materials in order to meet MRB turnaround time KPI.
  • Closely follow-up of individual Nonconformance/ CAPA/ SCAPA to drive issue closure at timely manner.
  • Communication of material quality issue and work on resolving the issue.
  • Work on reviewing and approving new supplier selection & evaluation and component qualification.
  • Demonstrate knowledge of national and international requirements and standards such as FDA QSR, ISO 13485, ISO 9001 and others.
  • Follow applicable procedure and other applicable policies and procedures in the review or development of control plans and approve supplier control plans.

Requirements:

  • Bachelor degree qualified
  • 2-5 years relevant experience in supplier quality management is preferred.
  • Working knowledge of FDA QSR, ISO9001 and/or ISO13485 is preferred.
  • Engineering tools utilization experience such as design of experiment, risk management, validation and statistical analysis is an asset.
  • ASQ Certified CQE, CQA or CRE is an asset.
  • 6 Sigma Green or Black Belt is also an asset
  • Effective verbal and written communication skills
  • Travel may be required in order to perform supplier assessments/audits and development.


To apply, please click "Apply Now" or visit www.gmprecruit.com and search for job reference: 18962

We regret that only shortlisted candidates will be notified.


GMP Technologies (S) Pte Ltd | EA Licence: 11C3793 | EA Personnel: Tan Wai Peng | Registration No: R1104671

EA License No.

09C3051

EA Personal Registration No.

R1104671
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Job ID: 18962

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