Quality & Regulatory Director (Medical Devices)
פורסם אתמול · 0 מועמדים
- B.Sc. in Engineering
- Minimum 10 years of experience backed by strong professional references
- Proven track record in management and team leadership
- ISO 13485 Lead Auditor certification
- Full professional proficiency in English (written and spoken)
חולץ מתיאור המשרה · מתעדכן אוטומטית
תיאור המשרה המלא
המשרה המקורית · נשמר לעיוןQuality & Regulatory Director (Medical Devices)
Location: Tel Aviv
Employment Type: Full-time
About Us
A leading boutique consultancy specializing in accelerating regulatory approvals, quality assurance, certification, and clinical trials for the medical device industry. Partnering with top multinational corporations, serial entrepreneurs, and cutting-edge startups,
The Role
We are seeking an experienced Quality & Regulatory Director to join our senior leadership team. In this high-impact position, you will drive project strategy, create exceptional value for our clients, and ensure both technical precision and commercial efficiency.
Key Responsibilities:
· Lead complex Quality Assurance (QA) and Regulatory Affairs (RA) projects for diverse MedTech clients.
· Define and execute regulatory strategies to achieve timely global market clearances.
Requirements
· Education: B.Sc. in Engineering (Required).
· Experience: Minimum 10 years of experience in a medical device manufacturing company, backed by strong professional references.
· Leadership: Proven track record in management and team leadership.
· Certifications: ISO 13485 Lead Auditor certification.
· Languages: Full professional proficiency in English (written and spoken).
· Soft Skills: Outstanding service orientation, excellent interpersonal skills, and the ability to navigate complex stakeholder environments.
· Drive: Strong passion for medical device innovation and a desire to excel.
* The position is open to all qualified male and female applicants.
שאלות על המשרה
- המשרה לא ציינה שכר. אנחנו מציגים שכר רק כשהמעסיק מפרסם אותו.
- B.Sc. in Engineering, Minimum 10 years of experience backed by strong professional references, Proven track record in management and team leadership, ISO 13485 Lead Auditor certification, Full professional proficiency in English (written and spoken)