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.

 Requirements

• Bachelors degree required

• Minimum 3-5 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 in order to effectively communicate with internal customers and suppliers, and to develop and present communication plans and strategies.
• Proficient in the use of Microsoft Word, Excel and PowerPoint.

To find out more about this opportunity, please contact Lionel Liew at lionel.liew@gmprecruit.com.

We regret that only shortlisted candidates will be notified.

GMP Technologies (S) Pte Ltd   |   EA Licence: 11C3793 |   EA Personnel: Lionel Liew   |   Registration No: R1330693