Quality Engineer
פורסם לפני 19 ימים · 71 מועמדים
התפקיד במילים פשוטות
מהנדס/ת אבטחת איכות עיצוב מצטרף/ת לצוות בישראל. התפקיד כולל אחריות על אבטחת איכות בתהליכי תכנון ופיתוח מוצרים, מתן פתרונות מהירים לבעיות, ובקרת תיעוד פרויקטים. כמו כן, התפקיד דורש ייצוג צרכי אבטחת איכות מול לקוחות וסיוע בחקירת חריגות.
- At least 2 year of experience in working according to GMP and regulatory requirements (FDA QSR part 820, ISO 13485)
- Good knowledge of MS-Office tools (Excel, Word)
- Acquaintance with E-Document management systems
- English - high level (written and spoken)
- Experience in the field of Medical Devices
- Practical Engineer/ B.Sc. in Quality/ Biomedical/ Biotechnology or similar
- CMQ / CQE or similar
חולץ מתיאור המשרה · מתעדכן אוטומטית
למי זה מתאים
התפקיד מתאים למהנדסים/ות בעלי/ות שנתיים ניסיון לפחות בעבודה לפי דרישות GMP ורגולציה (FDA QSR חלק 820, ISO 13485). יתרון משמעותי לבעלי/ות ניסיון קודם באבטחת איכות תכנון, ניסיון עם QMS וייצור, וניסיון בתחום המכשור הרפואי.
תיאור המשרה המלא
המשרה המקורית · נשמר לעיוןAbout us
LTS is a leading pharmaceutical technology company that develops and manufactures innovative drug delivery systems for the pharmaceutical industry.
LTS´ commercial offering encompasses more than 20 marketed products.
LTS operates today from 5 sites: Netanya (Israel), Adrenarche (Germany), West Caldwell (NJ, USA), St. Paul (MN, USA), and Shanghai (China).
About the role
We are looking for an excellent Design QA Engineer to join our team in Israel.
The position is hybrid - 4 days a week from the office, and 1 day from home.
Responsibilities:
Be the QA focal point design and development of projects throughout the product design process until transfer to production
Provide quick solutions to inquires and problems arising during the process
Control all aspects of project documentation
Interface with relative personnel to resolve document problems/issues within the design process
Be a customer facing team member and represent the organization and QA needs to the customer
Assist in cases of non-conformities (NC) of products, parts and processes
Supporting production readiness activities and validations
Perform investigations and collect data on deviations of parts, materials or processes throughout the organization, while working with other departments
Direct manager: QA Manager
Job Requirements:
Education:
Practical Engineer/ B.Sc. in Quality/ Biomedical/ Biotechnology or similar - an advantage
CMQ / CQE or similar - an advantage
Job skills:
At least 2 year of experience in working according to GMP and regulatory requirements (FDA QSR part 820, ISO 13485) – mandatory
Previous experience in QA design work – significant advantage
Experience with QMS and production - significant advantage
Experience in the field of Medical Devices - an advantage
Computer skills:
Good knowledge of MS-Office tools (Excel, Word),
Acquaintance with E-Document management systems
Language skills:
English - high level (written and spoken)
Personality:
At LTS, we value collaboration, innovation, and accountability.
We're looking for individuals who can:
Teamwork: Collaborate effectively, embracing diverse perspectives.
Customer Focus: Exceed internal and external customer needs.
Innovation: Create new opportunities with enthusiasm.
Accountability: Take ownership of challenges, uphold standards.
Leadership: Motivate and develop talents, achieving goals.
Show more
Show less
שאלות על המשרה
- המשרה לא ציינה שכר. אנחנו מציגים שכר רק כשהמעסיק מפרסם אותו.
- היברידי
- At least 2 year of experience in working according to GMP and regulatory requirements (FDA QSR part 820, ISO 13485), Good knowledge of MS-Office tools (Excel, Word), Acquaintance with E-Document management systems, English - high level (written and spoken)