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

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

Supplier Quality Engineer (Medical Devices/ East)

GMP TECHNOLOGIES (S) PTE LTD Singapore Permanent
4,500 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 perceived gaps in process performance.

·                     Establish and successfully execute our supplier management and development plans which will align to overall business objectives.

·                     Communication of Medtronic expectations, in collaboration with MDT sourcing and/or MDT procurement functions, for continuous improvements and providing leadership for improving the supplier relationship. Work with them constructively to improve their performance levels.

·                     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 with Sister Facilities/ Suppliers, MDT sourcing and/or MDT procurement functions to resolve the issue.

·                     Work closely with MDT sourcing and/or MDT procurement functions in 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.

·                     Create or revise any procedure or documentation required to improve quality control between our suppliers and our company.

·                     Responsible for MSO in-house MCRD Identity Testing process.

·                     Follow applicable Medtronic procedure and other applicable policies and procedures in the review or development of control plans and approve supplier control plans.

·                     Travel may be required in order to perform supplier assessments/audits and development.

·                     Perform other duties as assigned.

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 perceived gaps in process performance.

·                     Establish and successfully execute our supplier management and development plans which will align to overall business objectives.

·                     Communication of Medtronic expectations, in collaboration with MDT sourcing and/or MDT procurement functions, for continuous improvements and providing leadership for improving the supplier relationship. Work with them constructively to improve their performance levels.

·                     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 with Sister Facilities/ Suppliers, MDT sourcing and/or MDT procurement functions to resolve the issue.

·                     Work closely with MDT sourcing and/or MDT procurement functions in 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.

·                     Create or revise any procedure or documentation required to improve quality control between our suppliers and our company.

·                     Responsible for MSO in-house MCRD Identity Testing process.

·                     Follow applicable Medtronic procedure and other applicable policies and procedures in the review or development of control plans and approve supplier control plans.

·                     Travel may be required in order to perform supplier assessments/audits and development.

·                     Perform other duties as assigned.

 

EA License No.

09C3051

EA Personal Registration No.

R1330693
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