Production and supplier Quality Engineer
פורסם לפני 20 ימים · 56 מועמדים
התפקיד במילים פשוטות
תפקיד זה כולל תמיכה ביציבות הייצור, בקרת מכשירי בדיקה אוטומטיים (ATE) וניהול תהליכי איכות מול ספקים. העובד יעסוק בחקירת תקלות ואירועי RMA/DOA, הובלת שיפורים מתמידים ותמיכה בשינויים הנדסיים (ECO/ECR). כמו כן, התפקיד דורש עבודה צמודה עם צוותי פיתוח וייצור ושמירה על תאימות לתקני מכשור רפואי.
- Bachelor’s degree in Engineering (Mechanical, Electrical, Biomedical, or related field)
- 3+ years of experience in Quality
- Strong analytical and problem-solving skills, including hands-on experience with RCA tools (5-Why, Fishbone, etc.)
- Excellent communication and collaboration skills
- Fluent in English
- Familiarity with ATE systems, production testing, and/or field reliability analysis
חולץ מתיאור המשרה · מתעדכן אוטומטית
למי זה מתאים
התפקיד מתאים למהנדסים בעלי תואר ראשון בהנדסה (מכונות, חשמל, ביו-רפואה וכדומה) עם לפחות 3 שנות ניסיון בתחום האיכות. הוא פחות יתאים למי שאין לו ניסיון בניתוח גורמי שורש (RCA) או למי שאינו שולט בשפה האנגלית.
תיאור המשרה המלא
המשרה המקורית · נשמר לעיוןDepartment: Quality
Location: EMEA-Israel
Description
About this opportunity
We are seeking a highly motivated and experienced Production and Suppliers Quality Engineer to drive exceptional product quality, patient safety, and field reliability across the Installed Base (IB). This is a key technical role supporting production stability, RMA/DOA investigations, Automated Test Equipment (ATE) performance, and cross-functional quality engineering initiatives in a regulated medical device environment.
Key Responsibilities
In this role, you will:
• Support qualifications and control of ATE testers in V&V phase and production lines.
• Support ECO/ECR processes, NPI projects, product updates, and cross-functional engineering changes.
• Participate in supplier selection and conduct suppliers’ audits
• Work closely with R&D, engineering, manufacturing, and operations teams to enhance product quality
and resolve technical issues.
• Drive continuous improvement initiatives using tools such as Six Sigma, Lean, and Root Cause Analysis (RCA).
• . Support RMA/DOA processes and continuous reduction of field failures
• Ensure compliance with ISO 13485, FDA 21 CFR 820, MDR, and other applicable medical device regulations.
• Maintain and support quality documentation, including CAPA, Non-Conformance Reports (NCRs), and risk management documentation.
Skills, Knowledge & Expertise
• Bachelor’s degree in Engineering (Mechanical, Electrical, Biomedical, or related field).
• 3+ years of experience in Quality, medical device experience is a strong advantage.
• Strong analytical and problem-solving skills, including hands-on experience with RCA tools (5-Why, Fishbone, etc.).
• Familiarity with ATE systems, production testing, and/or field reliability analysis — a strong advantage.
• Working knowledge of ISO 13485, FDA 21 CFR 820, and ISO 14971 risk management.
• Excellent communication and collaboration skills, with the ability to work effectively across functions.
• A proactive, structured, and detail-oriented working style.
• Fluent in English.
Applicant Privacy Policy
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Equal Opportunity Statement
Align Technology is an equal opportunity employer. We are committed to providing equal employment opportunities in all our practices, without regard to race, color, religion, sex, national origin, ancestry, marital status, protected veteran status, age, disability, sexual orientation, gender identity or expression, or any other legally protected category. Applicants must be legally authorized to work in the country for which they are applying, and employment eligibility will be verified as a condition of hire.
שאלות על המשרה
- המשרה לא ציינה שכר. אנחנו מציגים שכר רק כשהמעסיק מפרסם אותו.
- Bachelor’s degree in Engineering (Mechanical, Electrical, Biomedical, or related field), 3+ years of experience in Quality, Strong analytical and problem-solving skills, including hands-on experience with RCA tools (5-Why, Fishbone, etc.), Excellent communication and collaboration skills, Fluent in English