Quality Assurance engineers work alongside product managers, project managers, and developers to ensure quality is maintained at every development and distribution lifecycle stage.
Essential Functions
Handling customer complaints - documentation, investigation and regulatory assessment
Handling training requirements at the organizational level.
Training employees on quality issues in accordance with regulatory requirements.
Performing internal audits.
Writing work procedures.
support supplier audits and supplier assessment.
Requirements: Education: machinery/industry and management/quality/biotechnology
At least 3 years of experience in quality engineering or Quality Assurance in the medical device industry - mandatory.
Familiarity with regulatory standards and requirements in the medical products industry
High motivation, reliability, integrity and high interpersonal communication skills.
Order and organization at a high level, ability to understand specifications, drawings and data sheets - a must.
Ability to work in a team as well as the ability to work and be self-motivated.
Ability to work under pressure
Knowledge of Hebrew at mother tongue level, English at high level - mandatory.
Certified auditor for internal and supplier audits in medical device systems - an advantage.
Experience in the Priority system.
This position is open to all candidates.
