Quality & Regulatory Director (Medical Devices) Tel Aviv
פורסם אתמול · 0 מועמדים
- B.Sc. in Engineering
- Minimum 10 years of experience
- 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)
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, Proven track record in management and team leadership, ISO 13485 Lead Auditor certification, Full professional proficiency in English (written and spoken)