דרושים » ביוטכנולוגיה » QA Engineer - Complaints Investigator

משרות על המפה
 
בדיקת קורות חיים
VIP
הפוך ללקוח VIP
רגע, משהו חסר!
נשאר לך להשלים רק עוד פרט אחד:
 
שירות זה פתוח ללקוחות VIP בלבד
AllJObs VIP
סגור
דיווח על תוכן לא הולם או מפלה
מה השם שלך?
תיאור
שליחה
סגור
v נשלח
תודה על שיתוף הפעולה
מודים לך שלקחת חלק בשיפור התוכן שלנו :)
לפני 15 שעות
Location: Yokne'Am Illit
Job Type: Full Time
The Complaints Investigator will be responsible to Conduct costumer complaint investigations, identify root causes and issue an investigation report. Additionally support reportability assessment to the FDA.

Main responsibilities:

Conduct and lead customer complaint investigation related to mechanical issues, hardware issues, software issues, handling issues or production issues.
Work closely with the representative team in order to understand the nature of the complaint.
Work closely with SW and HW engineers, as well as the product team to determine the root cause of failure and ensure investigations are in compliance with the companys applicable policies.
Communicate and escalate investigation results and facilitate failure investigation decision process.
Provide recommendations to prevent failure recurrence and support for nonconformance/CAPA and ECO actions.
Requirements:
Bachelors degree in engineering: BSc Biomedical / Electrical / Mechanical engineering / Materials A must.
Minimum of 2 years experience as a complaints investigator or CAPA management - A must.
Proven experience in leading complaints investigations of a multidisciplinary system, preferably in the medical device industry.
knowledge of investigative and failure analysis techniques is preferred, experience in various root cause analysis method (e.g., fish bone diagrams, decision trees, etc..) and other quality tools is required.
Ability to write and communicate clearly in English, including generating and presenting well-written reports is required.
Ability to work in an evolving, challenging, multi-disciplinary environment with multiple tasks/projects.
Excellent prioritizing, organizational, and interpersonal skills.
A get-it-done attitude.
This position is open to all candidates.
 
Hide
הגשת מועמדותהגש מועמדות
עדכון קורות החיים לפני שליחה
עדכון קורות החיים לפני שליחה
8225765
סגור
שירות זה פתוח ללקוחות VIP בלבד
משרות דומות שיכולות לעניין אותך
סגור
דיווח על תוכן לא הולם או מפלה
מה השם שלך?
תיאור
שליחה
סגור
v נשלח
תודה על שיתוף הפעולה
מודים לך שלקחת חלק בשיפור התוכן שלנו :)
25/05/2025
חברה חסויה
Location: Yokne'Am Illit
Job Type: Full Time
we are a fast-growing medical device company focused on developing, manufacturing, and selling innovative devices for endovascular interventional procedures.= We are seeking a skilled and detail-oriented QA Engineer to join our team. The ideal candidate will be responsible for executing Quality Assurance activities, managing quality projects, and participating in process and product validations to ensure compliance with established standards and regulatory requirements. The QA Engineer will work closely with cross-functional teams to support quality projects, provide manufacturing support, and drive continuous improvement initiatives across the organization. LOCATION: Yokneam, Israel. The position includes the following responsibilities: SCOPE & RESPONSIBILITIES Manage ECOs: conduct risk assessment, update relevant DMR documents and carry out necessary IQ, OQ, PQ activities if required, finalization of implementation tasks. Manage DCOs in the PLM system : Write and update QA procedures to ensure compliance with quality standards and regulatory requirements. Manage NCR and CAPA processes: Lead, write and supervise the NCR and CAPA processes, ensuring timely and effective resolutions. Manage QA production activities: Provide quality support to production operations, addressing deviations and non-conformities to maintain high product quality. Ensuring Timely Resolution of Quality Issues: Promptly address all identified or assigned quality issues to prevent delays and maintain efficient operations. Participate in audits: Take part in internal and external audits, such as FDA inspections and notified body audits based on ISO13485, EUMDR, and MDSAP requirements.
Requirements:
Bachelor of Science degree or Engineering. 3-5 years of experience in medical device QA (ISO 13485, MDSAP, FDA QSR 820). Internal auditor certification- an advantage Ability to work in dynamic and multi-interfaced surroundings, micro and macro vision. Strong attention to details and Self-learning ability. Ability to manage time and priorities and work under pressure. English - high level (both written and spoken). Excellent leadership and people management skills. Service oriented. Knowledge and practical experience in Priority An advantage.
This position is open to all candidates.
 
Show more...
הגשת מועמדותהגש מועמדות
עדכון קורות החיים לפני שליחה
עדכון קורות החיים לפני שליחה
8191375
סגור
שירות זה פתוח ללקוחות VIP בלבד