oB.Sc in Biomedical\Biotechnology\Industrial Engineering
Proven experience as a team leader / group manager*
Proven experience as an SME in internal Audits*
o At least of 3 years Proven experience in the field of Medical Devices
o working in a medical device quality system framework (ISO 13485, QSR 21 CRF 820)
o Experience working in medical device product development (product design) and manufacturing (process design, process validation, and production).
oExpertise in FDA 21 CFR 820 regulations, ISO 13485, ISO 14971
oFull control of all MS-Office applications
•Computer skills: Full control of all MS-Office applications
•Language skills: Fluent English - writing and verbal.
oAbility to work under pressure and in tight schedules
oAbility to work in Multidisciplinary work opposite various stakeholders internally and externally
Position Location: Netanya