מנהל/ת יבוא/יצוא

Management of all quality system activities including, Internal Auditing, Quality Awareness Training, Supplier/Contract Manufacturing Organization (CMO) Auditing, Document Control, CAPA activities, Vigilance activities, MRB, Quality Improvement Meeting Continual improvement of Quality Assurance policies, procedures, and systems to ensure compliance with ISO and FDA compliance . Support the R&D activities related to all chemical aspects of product development. Managing the QA team in the company’s sites. Direct assistance to the VP QA/RA, and acting as a member of the RA/QA Management Group. Knowledge/Educational Requirements Extensive knowledge of ISO 13485 quality principles and requirements- a must! Extensive knowledge of ISO 13485 quality principles and requirements- a must! Good understanding of Medical Device Regulatory requirements 5 -7 years successful experience in Medical Device companies Bachelor’s degree and above in Life Science