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לפני 12 שעות
חברה חסויה
Location: Netanya
Job Type: Full Time
Job Description:

supplier approval/disapproval including supplier maintenance and issuance of the Approved Supplier List.

Leading the SCARS process including SCAR initiation, SCAR follow up, Supplier investigation approval including root cause analysis and SCAR closure.

Leading the supplier audits process (including initial and surveillance audits) for critical suppliers, service centers, laboratories etc. by conducting on site / remote audits. Issuance and execution of the supplier audits plan including supplier audits follow up and supplier non-conformance follow up and response approval.

Support the execution of service agreements, quality agreements with suppliers and service centers.

Leading the supplier score card process, including trending.

Serve as Eitan Medicals CAPA Coordinator and Subject Matter Expert
Responsible and accountable for CAPA ownership, timely execution, and effectiveness of CAPAs. This includes creation, collaboration with functional teams on Problem Statement writing/Scope identification/Risk Assessment/Containment/Correction/CAPA plans/Verification of local and global compliance to CAPA procedures to ensure timely effective closure of CAPAs.

Generate data and key quality trending information for use in periodic reviews like Quality Metric Reviews and Management Review for CAPA and supplier processes.

Work within, and ensure adherence to Quality System procedures, work instructions and other Quality System requirements.
Write, update, release, and sign quality documentation within the Quality management system.

Direct manager: QA Compliance Manager
Requirements:
Education:
Practical Engineer/ B.Sc. in Quality/ Biomedical/ Biotechnology or similar or CQM / CQE.

Job skills:
3-5 years of relevant experience.
Good knowledge of ISO 9001, ISO 13485 and international standards.
Knowledge and experience with quality processes.
Experience in the field of Medical Devices - an advantage.
Knowledge and experience in quality processes.
Auditor certificate - an advantage.

Computer skills:
Good knowledge of MS-Office tools (Excel, Word, PP).
Acquaintance with E-Document management systems.
Knowledge of statistical based computer programs such as Excel and/or Minitab.

Language skills:
English and Hebrew - fluent.

Personality:
Ability to evaluate, prioritize, organize, multitask and problem solving.
Ability to work in a team as well as independently
This position is open to all candidates.
 
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הגשת מועמדותהגש מועמדות
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לפני 19 שעות
Job Type: Full Time
A medical device company is seeking to hire a Quality Design Assurance Engineer to join our QA team. As a Design Assurance Engineer, you will lead all quality elements of Design Controls and product DHF for new product introductions and sustaining/design projects.
Responsibilities
Quality responsibility to verify that the design and development process follows the procedures and design and development plans.
Work closely with R D and TEST teams to support regulatory requirements by creating, reviewing, and providing quality and compliance input to the design and development process, deliverables, and requirements.
Participation in project meetings to review and help update clear and concise user requirements, product specifications, plans, verification and validation studies, risk management files, and other relevant design control deliverables.
Quality responsibility for transferring
Requirements:
At least 2-3 years of experience working in a quality function in the medical device industry - must.
At least 1 year of experience as a design control engineer (preferred).
Prior hands-on experience in Verification Validation (V V) activities within the medical device industry - a significant advantage.
A Bachelor of Science in Engineering, Sciences, or a related field - must.
Familiar with statistical techniques used in verification and validation processes - must.
Experience with ISO 14971, 21 CR 820, ISO 13485, EU MDR, IEC 60601-1, IEC 62366, and IEC 62304 standards - must.
Strong analytical and problem-solving skills, with keen attention to detail.
Excellent communication and interpersonal skills, with the ability to collaborate effectively across functions.
Proficient use of standard MS Office applications.
Fluent in English (oral and written
This position is open to all candidates.
 
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הגשת מועמדות
עדכון קורות החיים לפני שליחה
8680382
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תודה על שיתוף הפעולה
מודים לך שלקחת חלק בשיפור התוכן שלנו :)
לפני 23 שעות
Job Type: Full Time
A global leading medical device company in the field of neuromodulation and rehabilitation at Hod Hasharon is looking for a mechanical engineer.
Responsibilities
Leading mechanical changes in products.
Introduction of new products to manufacturing engineering and production.
Write and execute engineering TEST plans/reports and work instructions.
Design, build and TEST fixtures and jigs for production.
Investigate mechanical and system failures.
Guiding and training production line workers.
Provide technical assistance for the company's manufacturers.
Requirements:
B.Sc Mechanical Engineer or Biomedical Engineering.
3+ years of experience in mechanical design and engineering support in a production line.
Strong proficiency with 3D CAD modelling and mechanical design using SolidWorks, including detailed drawing creation, tolerance analysis, and GD T.
Strong oral and written communication skills, both Hebrew and English.
Good practical skills in prototyping.
Excellent technical skills, including computer-aid design experience.
Creativity and Problem-solving abilities.
Interpersonal and teamworking abilities.
Driving license.
Experience in writing and executing V V TEST plans
This position is open to all candidates.
 
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הגשת מועמדות
עדכון קורות החיים לפני שליחה
8617555
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תודה על שיתוף הפעולה
מודים לך שלקחת חלק בשיפור התוכן שלנו :)
 
משרה בלעדית
לפני 19 שעות
חברה חסויה
Location: More than one
Job Type: Full Time
The VP Clinical Applications is a senior leadership role responsible for shaping and executing the global clinical applications strategy across the company portfolio. The role bridges clinical practice, product development, and commercial activities to ensure strong clinical value, Customer Experience, and product adoption worldwide.
Requirements:
5+ years in clinical applications / Medical imaging including senior leadership roles.
Fluent English.
Experience leading global teams and supporting full product lifecycle.
Strong track record working with clinicians, hospitals, and KOLs.
Deep understanding of clinical NM diagnostic imaging workflows and medical imaging.
Familiarity with regulatory and clinical validation processes.
Knowledge of product development processes and cross-functional work in MedTech.
Strong leadership and stakeholder management in a matrix environment.
Excellent communication with clinical and executive audiences.
Strategic thinking with hands-on execution.
Strong problem-solving and organizational skills.
Ability to operate in a global, fast-paced environment.
Strong relationship-building internally and externally.
Willingness to travel internationally.
This position is open to all candidates.
 
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הגשת מועמדות
עדכון קורות החיים לפני שליחה
8720967
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דיווח על תוכן לא הולם או מפלה
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סגור
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מודים לך שלקחת חלק בשיפור התוכן שלנו :)
12/06/2026
חברה חסויה
Location: Netanya
Job Type: Full Time
our company is an international Medical Device company that develops and manufactures innovative medical equipment. Specifically, we develop infusion pumps and their related accessory products. Job Description: supplier approval/disapproval including supplier maintenance and issuance of the Approved Supplier List. Leading the SCARS process including SCAR initiation, SCAR follow up, Supplier investigation approval including root cause analysis and SCAR closure. Leading the supplier audits process (including initial and surveillance audits) for critical suppliers, service centers, laboratories etc. by conducting on site / remote audits. Issuance and execution of the supplier audits plan including supplier audits follow up and supplier non-conformance follow up and response approval.
* Support the execution of service agreements, quality agreements with suppliers and service centers. Leading the supplier score card process, including trending.
* Serve as  CAPA Coordinator and Subject Matter Expert
* Responsible and accountable for CAPA ownership, timely execution, and effectiveness of CAPAs. This includes creation, collaboration with functional teams on Problem Statement writing/Scope identification/Risk Assessment/Containment/Correction/CAPA plans/Verification of local and global compliance to CAPA procedures to ensure timely effective closure of CAPAs Generate data and key quality trending information for use in periodic reviews like Quality Metric Reviews and Management Review for CAPA and supplier processes.
* Work within, and ensure adherence to Quality system procedures, work instructions and other Quality system requirements.
* Write, update, release, and sign quality documentation within the Quality management system
Direct manager: QA Compliance Manager
Requirements:
Education o Practical Engineer/ B.Sc. in Quality/ Biomedical/ Biotechnology or similar or CQM / CQE. Job skills:
* 3- 5 years of relevant experience.
* Good knowledge of ISO 9001, ISO 13485 and international standards. o Knowledge and experience with quality processes. o Experience in the field of Medical Devices - an advantage. o Knowledge and experience in quality processes o Auditor certificate - an advantage.
Computer skills: o Good knowledge of MS-Office tools (Excel, Word, PP). o Acquaintance with E-Document management systems. o Knowledge of statistical based computer programs such as Excel and/or Minitab
Language skills:
* English and Hebrew - fluent.
Personality:
* Ability to evaluate, prioritize, organize, multitask and problem solving.
* Ability to work in a team as well as independently
This position is open to all candidates.
 
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הגשת מועמדותהגש מועמדות
עדכון קורות החיים לפני שליחה
עדכון קורות החיים לפני שליחה
8691131
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תודה על שיתוף הפעולה
מודים לך שלקחת חלק בשיפור התוכן שלנו :)
14/06/2026
Location: Netanya
Job Type: Full Time
DRS RADA is a global pioneer of radar systems for active military protection, counter-drone applications, critical infrastructure protection, and border surveillance. We are looking for an experienced Program Manager to join our team. Job Description: Overall responsibility for managing, maintaining, and continuously improving the organization’s Quality Management System (QMS), including certification processes, internal and external audits, regulatory activities, and compliance oversight, while ensuring alignment with organizational objectives, applicable standards, procedures, customer requirements, and relevant compliance obligations. Key Responsibilities:
* Lead and manage the organization’s Quality Management System (QMS) end-to-end across development, project management, operations, and production.
* Ensure the establishment, implementation, maintenance, and continuous improvement of quality processes, procedures, and controls in alignment with applicable standards and organizational requirements.
* Manage and develop the quality and regulatory team, providing professional leadership across quality, regulatory, and compliance activities.
* Oversee certification activities, internal and external audits, and the effective management of nonconformities, corrective actions, and preventive actions.
* Lead regulatory and compliance activities to ensure adherence to applicable requirements, customer expectations, and organizational commitments.
* Monitor performance through quality metrics and management reporting, and drive a culture of quality, accountability, and continuous improvement across the organization.
Requirements:
* Experience in managing Quality Management Systems (QMS).
* In-depth knowledge of AS9100 and ISO 9001 standards.
* Previous managerial experience.
* Relevant academic degree.
* Experience in compliance and regulatory activities.
This position is open to all candidates.
 
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הגשת מועמדותהגש מועמדות
עדכון קורות החיים לפני שליחה
עדכון קורות החיים לפני שליחה
8692781
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דיווח על תוכן לא הולם או מפלה
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תיאור
שליחה
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תודה על שיתוף הפעולה
מודים לך שלקחת חלק בשיפור התוכן שלנו :)
26/06/2026
חברה חסויה
Location: Netanya
Job Type: Full Time
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 Research Engineer to join the R & D team. Job Description · Lead novel research in state-of-the-art technologies - bypass technological borders · Lead departmental tasks that include problem solving and critical/root cause analysis · Algorithms development for various system components · Design and implementation of experiments for various projects · Manage mutual research projects done and universities around the world Direct Manager: Research director
Requirements:
Education PhD in Engineering, preferably in Physics , Biomedical Engineering, Mechanical Engineering, or a related field Job skills · Proven experience in research and development within the medical device industry - significant advantage · Extensive knowledge in fluid dynamics, mechanics, and electronics · Advanced data analysis skills and experience with computer simulation tools · Excellent communication skills in English, including high-level technical writing ability · Ability to work independently while collaborating effectively in a multidisciplinary team · Creative thinking and complex problem-solving skills · Experience in leading research and development projects - advantage Computer skills o Proficiency in Office products – Must Language skills English – Good level Personality o Highly organized and detail oriented o Thoroughness, flexibility, and Operational capabilities o Excellent interpersonal relations o Initiative and highly motivated
This position is open to all candidates.
 
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הגשת מועמדותהגש מועמדות
עדכון קורות החיים לפני שליחה
עדכון קורות החיים לפני שליחה
8645459
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דיווח על תוכן לא הולם או מפלה
מה השם שלך?
תיאור
שליחה
סגור
v נשלח
תודה על שיתוף הפעולה
מודים לך שלקחת חלק בשיפור התוכן שלנו :)
לפני 12 שעות
חברה חסויה
Location: Netanya
Job Type: Full Time
We are looking for an excellent Research Engineer to join the R & D team.

Job Description:
Lead novel research in state-of-the-art technologies - bypass technological borders.
Lead departmental tasks that include problem solving and critical/root cause analysis.
Algorithms development for various system components.
Design and implementation of experiments for various projects.
Manage mutual research projects done and universities around the world.


Direct Manager: Research director.
Requirements:
Education: PhD in Engineering, preferably in Physics , Biomedical Engineering, Mechanical Engineering, or a related field.

Job skills:
Proven experience in research and development within the medical device industry - significant advantage.
Extensive knowledge in fluid dynamics, mechanics, and electronics.
Advanced data analysis skills and experience with computer simulation tools.
Excellent communication skills in English, including high-level technical writing ability.
Ability to work independently while collaborating effectively in a multidisciplinary team.
Creative thinking and complex problem-solving skills.
Experience in leading research and development projects - advantage

Computer skills:
Proficiency in Office products - Must.
Language skills: English - Good level.

Personality:
Highly organized and detail oriented.
Thoroughness, flexibility, and Operational capabilities.
Excellent interpersonal relations.
Initiative and highly motivated.
This position is open to all candidates.
 
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הגשת מועמדותהגש מועמדות
עדכון קורות החיים לפני שליחה
עדכון קורות החיים לפני שליחה
8723943
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שירות זה פתוח ללקוחות VIP בלבד
סגור
דיווח על תוכן לא הולם או מפלה
מה השם שלך?
תיאור
שליחה
סגור
v נשלח
תודה על שיתוף הפעולה
מודים לך שלקחת חלק בשיפור התוכן שלנו :)
28/05/2026
חברה חסויה
Location: Netanya
Job Type: Full Time
Responsibilities
Support the maintenance and organization of the Design History File (DHF) documentation.
Assist in completing documentation required for product releases in compliance with FDA, CE, ISO, and internal procedures.
Provide administrative support for design control activities throughout the product development lifecycle.
Support documentation related to software validation and traceability.
Assist in preparing documentation for audits and regulatory submissions.
Ensure documentation is accurate, complete, and properly filed in internal systems.
Requirements:
BSc in Biomedical Engineering, Biotechnology, Life Sciences, or a related field.
1+ years of experience in quality management / regulated medical device environments.
Ability to manage multiple documents and tasks simultaneously.
Strong computer skills.
Proactive attitude and willingness to learn.
Strong organizational and communication skills and high attention to detail.
Prior experience in documentation/administrative roles - an advantage.
This position is open to all candidates.
 
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הגשת מועמדותהגש מועמדות
עדכון קורות החיים לפני שליחה
עדכון קורות החיים לפני שליחה
8670260
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סגור
דיווח על תוכן לא הולם או מפלה
מה השם שלך?
תיאור
שליחה
סגור
v נשלח
תודה על שיתוף הפעולה
מודים לך שלקחת חלק בשיפור התוכן שלנו :)
29/05/2026
חברה חסויה
Location: Netanya
Job Type: Full Time
our company 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 Research Engineer to join the R & D team. Job Description Lead novel research in state-of-the-art technologies - bypass technological borders Lead departmental tasks that include problem solving and critical/root cause analysis Algorithms development for various system components Design and implementation of experiments for various projects Manage mutual research projects done and universities around the world
Requirements:
* Masters degree graduate in Engineering, preferably in Physics, Biomedical Engineering, Mechanical Engineering, or a related field- MUST
* Relevant experience in research and development; experience in the medical device industry is a significant advantage
* Extensive knowledge in fluid dynamics, mechanics, and electronics
* Advanced data analysis skills and experience with computer simulation tools
* Excellent communication skills in English, including high-level technical writing ability
* Ability to work independently while collaborating effectively in a multidisciplinary team
* Creative thinking and complex problem-solving skills
This position is open to all candidates.
 
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הגשת מועמדותהגש מועמדות
עדכון קורות החיים לפני שליחה
עדכון קורות החיים לפני שליחה
8671416
סגור
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סגור
דיווח על תוכן לא הולם או מפלה
מה השם שלך?
תיאור
שליחה
סגור
v נשלח
תודה על שיתוף הפעולה
מודים לך שלקחת חלק בשיפור התוכן שלנו :)
לפני 12 שעות
חברה חסויה
Location: Netanya
Job Type: Full Time
We are looking for an excellent Research Engineer to join the R & D team.


Job Description:

Lead novel research in state-of-the-art technologies - bypass technological borders.

Lead departmental tasks that include problem solving and critical/root cause analysis.

Algorithms development for various system components.

Design and implementation of experiments for various projects.

Manage mutual research projects done and universities around the world.
Requirements:
Masters degree graduate in Engineering, preferably in Physics, Biomedical Engineering, Mechanical Engineering, or a related field- MUST.
Relevant experience in research and development; experience in the medical device industry is a significant advantage.
Extensive knowledge in fluid dynamics, mechanics, and electronics.
Advanced data analysis skills and experience with computer simulation tools.
Excellent communication skills in English, including high-level technical writing ability.
Ability to work independently while collaborating effectively in a multidisciplinary team.
Creative thinking and complex problem-solving skills.
This position is open to all candidates.
 
Show more...
הגשת מועמדותהגש מועמדות
עדכון קורות החיים לפני שליחה
עדכון קורות החיים לפני שליחה
8723947
סגור
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