You will

Plan and Support all QC activities Monitor non-conformance failures, including root cause analysis & corrective actionsParticipate in 8D investigations of production nonconforming products Develop and document work instruction procedures Plan, conduct and participate in internal manufacturing audits Monitor the entire production cycle and perform tests to identify potential malfunctions Participate In the ECM committee and QMS approval processesPrepare monthly quality reports of operations malfunctions and corrective actionsSupport all training activities related to operation quality procedures Participate in risk analysis team PFMEA and monitor the AI’sPromote initiatives to improve quality

You have

B.Sc. degree in engineering or equivalent- MustCQE Diploma – Advantage4-5 years of experience in a quality assurance position in Medical Device / Pharma industries/ Semiconductor Industry - MustExperience and knowledge with the ISO 9001:2015 standard- MustFluent English (read, write & talk) – MustQuality processes knowledge such as ECO, NCR, MRB, FMEA, 8D investigationsProficiency in Microsoft Office, Excel, and PowerPointExperience with working in controlled environment (clean room) – AdvantageExperience with ERP systems such as Priority – Advantage

Your ZEISS Recruiting Team:

Rital Ben-Porat, Tali Ytzhaki (טלי יצחקי)