תיאור המשרה המלא
המשרה המקורית · נשמר לעיוןWe're looking for a motivated QA/RA Student to join our Quality & Regulatory team and gain hands-on experience in the medical device industry while supporting quality processes and regulatory compliance.
Responsibilities
• Support the day-to-day maintenance and administration of the Quality Management System (QMS).
• Perform hands-on QA and QC activities, including inspection, completion of quality forms, and maintenance of related records.
• Assist with the preparation, organization, and review of quality documentation in accordance with ISO 13485:2016 and internal quality activities.
• Support document control activities, including document filing, organization, status tracking, updates, and distribution.
• Maintain and update quality records, logs, trackers, and databases, including data collection, cross-checking, and follow-up to ensure information is complete, accurate, and up to date.
• Support QMS activities, including CAPA, NCR, Change Control, Supplier Quality, training, and other quality processes, including follow-up on related quality actions.
• Support Design Control activities, including document tracking and administrative support.
• Support production activities by assisting with quality-related tasks, inspections, documentation, and follow-up.
• Collaborate with cross-functional teams including R&D, Operations, and Manufacturing to collect information and support quality activities.
Requirements
• B.Sc. student in Biomedical Engineering, Biotechnology, Industrial Engineering, Life Sciences, or a related discipline.
• Availability of at least 2–3 working days per week.
• Strong attention to detail and excellent organizational skills.
• High level of English (reading and working with technical documentation).
• Good communication and teamwork skills.
• Ability to work independently and manage multiple tasks.
• Willingness to perform hands-on administrative and operational tasks as part of the daily work.
שאלות על המשרה
- המשרה לא ציינה שכר. אנחנו מציגים שכר רק כשהמעסיק מפרסם אותו.