As a Quality Engineer, you will be responsible for NPI products transfer from development to production, validation activities , supporting activities related to process and production quality improvements, non-conforming products process management

The Quality Engineer is mainly responsible for:

• Leading NPI product transfer from development to production
• Manage process validation, including supplier guidance.
• Manage Supplier related activities ( Review and approve supplier nonconformance, Investigations and lead improvement plans with the suppliers)
• Manage activities related to nonconformance methodology (nonconformance follow up and reports, and product dispositions).
• Experience with validations (IQ/OQ/PQ/TMV) and supplier management
• Conduct and support NC investigations (internal and supplier non-conformances).
• Performing analysis of nonconforming products and presenting data in monthly meetings.
• Support the production team in analyzing and reporting the quality event.

Qualifications - External

• BSc in Engineering/ BA degree or Practical Engineering with Qualification in Quality Assurance (CQE).
• At least 4 years experience in medical systems or medical device companies
• Knowledge of investigations & cause analysis.
• Demonstrated knowledge of manufacturing process principles, practices, and procedures.
• Leading multidisciplinary project and processes
• Good communication skills, both verbal and written in English.
• Good interpersonal relations, reliable and accurate, sense of urgency, and a team player.