- Manage the quality system and work with regulatory bodies and the production line.
- Coordinate work in accordance with internal and external specifications and standards.
- Write, review, and approve company documents, specifications, and procedures.
- Improve processes, participate in internal audits, and carry out corrective and preventive actions.
- Manage change control activities and monitor design development activities.
Requirements: - Bachelor's degree (BSc) or higher in life sciences, biology, chemistry, biotechnology, or related fields - required.
- Must possess extensive knowledge of quality requirements.
- Experience and understanding of regulatory requirements in the Medical Device field.
- At least 5 years of experience in the medical device industry.
- Fluent in English.
.המשרה מיועדת לנשים ולגברים כאחד