ירושלים, ישראל

תיאור

• 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

דרישות

• 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.
• Ability to work under pressure.
• 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.
• Certified auditor for internal and supplier audits in medical device systems - an advantage.
• Experience in the Priority system.
• Preparing reports and performing statistical analyses.
• Great attention to detail and problem-solving abilities
• Good analytical skills
• Experience in a manufacturing environment.
This position is open to all candidates.