Multidisciplinary Verification & Validation (V&V) engineering for medical device
פורסם לפני 24 ימים · 0 מועמדים
התפקיד במילים פשוטות
מהנדס/ת אבטחת איכות תכנון בחברת מכשור רפואי יוביל את כל היבטי האיכות של בקרות תכנון ו-DHF מוצר עבור השקות מוצרים חדשים ופרויקטים מתמשכים. התפקיד כולל אחריות איכותית לוודא שתהליך התכנון והפיתוח עומד בנהלים ובתוכניות, עבודה צמודה עם צוותי מחקר ופיתוח ובדיקות, ותמיכה בדרישות רגולטוריות.
- At least 2-3 years of experience working in a quality function
- A Bachelor of Science in Engineering, Sciences, or a related field
- Familiar with statistical techniques used in verification and validation processes
- Experience with ISO 14971, 21 CR 820, ISO 13485, EU MDR, IEC 60601-1, IEC 62366, and IEC 62304 standards
חולץ מתיאור המשרה · מתעדכן אוטומטית
למי זה מתאים
התפקיד מתאים למהנדסים/ות בעלי/ות לפחות 2-3 שנות ניסיון בתחום האיכות בתעשיית המכשור הרפואי, ורצוי עם ניסיון בבקרת תכנון. נדרש תואר ראשון בהנדסה או מדעים והיכרות עם תקנים רלוונטיים בתעשייה.
תיאור המשרה המלא
המשרה המקורית · נשמר לעיוןA medical device company near Netanya is seeking to hire a Quality Design Assurance Engineer to join our QA team. As a Design Assurance Engineer, you will lead all quality elements of Design Controls and product DHF for new product introductions and sustaining/design projects.
Responsibilities
Quality responsibility to verify that the design and development process follows the procedures and design and development plans.
Work closely with R&D and test teams to support regulatory requirements by creating, reviewing, and providing quality and compliance input to the design and development process, deliverables, and requirements.
Participation in project meetings to review and help update clear and concise user requirements, product specifications, plans, verification and validation studies, risk management files, and other relevant design control deliverables.
Quality responsibility for transferring new products and sustaining projects to manufacturing and operations quality and supplier quality teams.
Support the Regulatory Affairs department for submissions and respond to submission questions, implementation of new or revised standards and support internal and external audits.
דרישות
At least 2-3 years of experience working in a quality function in the medical device industry – must.
At least 1 year of experience as a design control engineer (preferred).
Prior hands-on experience in Verification & Validation (V&V) activities within the medical device industry – a significant advantage.
A Bachelor of Science in Engineering, Sciences, or a related field – must.
Familiar with statistical techniques used in verification and validation processes – must.
Experience with ISO 14971, 21 CR 820, ISO 13485, EU MDR, IEC 60601-1, IEC 62366, and IEC 62304 standards – must.
Strong analytical and problem-solving skills, with keen attention to detail.
Excellent communication and interpersonal skills, with the ability to collaborate effectively across functions.
Proficient use of standard MS Office applications.
Fluent in English (oral and written).
מיומנויותTips: Provide a summary of the role, what success in the position looks like, and how this role fits into the organization overall.
Responsibilities
[Be specific when describing each of the responsibilities. Use gender-neutral, inclusive language.]
Example: Determine and develop user requirements for systems in production, to ensure maximum usability
Qualifications
[Some qualifications you may want to include are Skills, Education, Experience, or Certifications.]
Example: Excellent verbal and written communication skills
שאלות על המשרה
- המשרה לא ציינה שכר. אנחנו מציגים שכר רק כשהמעסיק מפרסם אותו.
- At least 2-3 years of experience working in a quality function, A Bachelor of Science in Engineering, Sciences, or a related field, Familiar with statistical techniques used in verification and validation processes, Experience with ISO 14971, 21 CR 820, ISO 13485, EU MDR, IEC 60601-1, IEC 62366, and IEC 62304 standards