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.
Technical writing skills that include quality procedures and TEST plans
Support supplier audits and supplier assessment.
Monitoring the entire production cycle and reporting on malfunctions
Problem-solving abilities and attention to detail.
Identify the root of technical issues and recommend fixes
Handling training requirements at the organizational level.
Training employees on quality issues in accordance with regulatory requirements.
Performing internal audits.
Technical writing skills that include quality procedures and TEST plans
Support supplier audits and supplier assessment.
Monitoring the entire production cycle and reporting on malfunctions
Problem-solving abilities and attention to detail.
Identify the root of technical issues and recommend fixes
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.
Attention to details, 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.
Willing to travel to the northern part of the country.
High articulateness, systemic vision, ability to pursue goals and meet goals.
Knowledge of Hebrew at mother tongue level, English at high level – mandatory.
Experience in the Priority system
Experience in a manufacturing environment.
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.
Attention to details, 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.
Willing to travel to the northern part of the country.
High articulateness, systemic vision, ability to pursue goals and meet goals.
Knowledge of Hebrew at mother tongue level, English at high level – mandatory.
Experience in the Priority system
Experience in a manufacturing environment.
This position is open to all candidates.
