- מיקום
- כל הארץ
- היקף משרה
- משרה מלאה
- תפקיד
- בודק/ת תוכנה (QA)
תיאור המשרה
Responsibilities:
- Support and maintain Quality Management System %28QMS%29 processes in accordance with applicable regulations and standards.
- Contribute to quality activities across the product lifecycle, including development and manufacturing-related processes.
- Participate in the preparation, review, and maintenance of quality documentation such as procedures and work instructions.
- Collaborate with cross-functional teams to support quality objectives and continuous improvement.
- Support compliance with regulatory and quality standards, including ISO 13485.
- Participate in internal and external audits as needed.
Requirements
- 5+ years of experience in Quality Assurance within the medical device industry.
- BSc in a relevant scientific or engineering discipline.
- Familiarity with medical device quality processes %28e.g., risk management, design controls, manufacturing-related quality activities%29.
- Strong written and verbal communication skills in English; Hebrew is an advantage.
- High attention to detail and strong organizational skills.
- Ability to work both independently and as part of a team in a dynamic environment.
