Job Description

Eitan Medical is a fast-growing global medical device company, developing and manufacturing innovative drug delivery and infusion solutions across the continuum of care- from the hospital to the home. We are looking for an excellent Production Quality Engineer to join the QA product team

• Serve as owner of the NCMR process: manage the end-to-end handling of non-conforming materials, products, and processes, including initiation, investigation and corrective/preventive actions in accordance with company procedures and regulatory requirements.
• Monitor NCMR process including quality KPI’s
• Support for non-conformity investigations and assign effective corrective actions for NCMRs and ensure timely closure and documentation.
• Perform / review Root Cause Analysis as part of NCMR process and assign relevant corrective actions.
• Act as QA representative for Manufacturing Quality process
• Conduct quality assurance activities such as data analysis and statistical evaluations, SOP review and approvals, audit preparation

Direct Manager: Manufacturing Quality Manager

Requirements

Requirements:

· Education: B.Sc. in BiomedicalBiotechnologyChemical Engineering

Job skills:

• 2 -5 years of experience in QA/RA, in a medical device or pharma manufacturing company

· Deep knowledge in working according to Medical device regulations and GMP (FDA QSR 820, ISO 13485)

Auditor qualification - an advantage

· Computer skills: Proficiency in Office products – Must. ERP systems, an advantage.

· Language skills: Fluent English - Mother tongue level

Personality:

Team player ,Excellent interpersonal relations, Highly organized and detail oriented, Motivated and committed ,Creative and proactive.

Assertive with the ability to effectively lead and drive cross-functional collaboration; capable of confidently interacting with multiple departments, assigning tasks, and ensuring timely execution.