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About The Position
- Responsible for nonconformance investigation in the production line and service departments.
- Define CAPA action plan with applicable departments/ vendors and verify proper implementation and CAPA closure.
- Responsible for parts inspection and nonconformance reporting in the operations department.
- Verify that received parts were manufactured according to the company purchasing requirements and communicate nonconformance to vendors.
- Communicate internal processes implementation nonconformance to applicable departments.
- Implement Medical devices QMS processes.
- Initiate and manage CAPA process to improve QMS processes documentation and implementation with applicable departments.
Requirements
- CQE / Mechanical / Bio-Medical / Industrial / Electrical technician or engineer is an advantage
- At least one year of experience as Quality engineer or as engineering engineer in medical devices companies or manufacturing facility.
- Experience with verification of the received parts according to purchasing requirements.
- Experience with the use and operation of measuring equipment.
- Experience with production line nonconformance investigation and CAPA process.
- Experience with subcontractors’ control
- Experience with subcontractors’ auditing – an advantage
- English and Hebrew - High level
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