You will
- Plan and Support all QC activities
- Monitor non-conformance failures, including root cause analysis & corrective actions
- Participate 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 processes
- Prepare monthly quality reports of operations malfunctions and corrective actions
- Support all training activities related to operation quality procedures
- Participate in risk analysis team PFMEA and monitor the AI’s
- Promote initiatives to improve quality
You have
- B.Sc. degree in engineering or equivalent- Must
- CQE Diploma – Advantage
- 4-5 years of experience in a quality assurance position in Medical Device / Pharma industries/ Semiconductor Industry - Must
- Experience and knowledge with the ISO 9001:2015 standard- Must
- Fluent English (read, write & talk) – Must
- Quality processes knowledge such as ECO, NCR, MRB, FMEA, 8D investigations
- Proficiency in Microsoft Office, Excel, and PowerPoint
- Experience with working in controlled environment (clean room) – Advantage
- Experience with ERP systems such as Priority – Advantage
Your ZEISS Recruiting Team:
Rital Ben-Porat, Tali Ytzhaki (טלי יצחקי)
Carl Zeiss Meditec AG
Carl Zeiss Meditec AG enables medical professionals worldwide to improve the lives of their patients in ophthalmology, microsurgery and other medical growth sectors.
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