JOB DETAILS

Production Quality Engineer

CompanyEitan Medical
LocationNetanya
Work ModeOn Site
PostedMay 10, 2026
About The Company
Eitan Medical is reimagining drug delivery with reliable innovation that puts patients at the center of care, making infusion easier and safer than ever before. Patient safety and care is only the starting point, as Eitan Medical goes beyond, delivering connected, intuitive infusion solutions that are designed to improve patients’ and clinicians’ quality of life across the continuum of care, including hospital, ambulatory care, and home care solutions. For over a decade, Eitan Medical and its global partners have provided safe, intuitive, and flexible infusion solutions that meet evolving drug delivery needs.
About the Role

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.

 

Job Description:

  • 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 Biomedical\Biotechnology\Chemical 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.

Key Skills
NCMR Process ManagementNon-Conforming Material HandlingCorrective ActionsPreventive ActionsRoot Cause AnalysisQuality KPI MonitoringSOP ReviewAudit PreparationData AnalysisStatistical EvaluationGMP ComplianceFDA QSR 820ISO 13485ERP SystemsInterpersonal SkillsCross-functional Collaboration
Categories
ManufacturingEngineeringHealthcareScience & Research
Job Information
📋Core Responsibilities
The engineer will own the Non-Conforming Material Review (NCMR) process, managing everything from initiation and investigation to implementing corrective and preventive actions according to regulatory requirements. This role also involves acting as the QA representative for manufacturing quality processes, including data analysis and SOP approvals.
📋Job Type
full time
📊Experience Level
2-5
💼Company Size
296
📊Visa Sponsorship
No
💼Language
English
🏢Working Hours
40 hours
Apply Now →

You'll be redirected to
the company's application page