Position QMS specialist
Administration of the CAPA system, assigning appropriate personnel to be the originators and approving and monitoring the completion of the preventive and corrective actions. Responsible for performing periodic analyses on corrective and preventive action requests collected over time to identify trends.
NC & Data management
QMS training sand processes improvements
Management review meeting and QRB meetings
Perform Internal audits plan and take part in external (regulatory, customers) audits.
Participate or lead different Quality plans as per need and relevance.
B.Sc in Engineering or practical engineer – life sciences
At least 3+ years’ experience in quality assurance, preferably with QMS management /projects, in a medical device or pharma manufacturing company according to GMP and regulatory requirements (FDA QSR 820, ISO 13485, 9001)
Proven experience in Audits (CE, FDA)- advantage
Computer skills: Full control of all MS-Office applications
Language skills: Fluent English - writing and verbal
To apply, send a resume to CV@LR-JOB.CO.IL
For details: 04-8383758