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דרושים חיפה
מהנדס /ת אפליקציות ציוד רפואי
לפני 16 דקותשלח קורות חייםהוסף לסל
optimumחברת ציוד רפואי בבנימינה מחפשת לתרגום דרישות קליניות של לקוחות לבניית אפיון טכני מערכתי בשיתוף עם אנשי פיתוח. איפיון ממשקים ברמת-על בין דיסציפלינות הנדסיות שונות.
דרישות התפקיד:מהנדס/ת ביורפואה עם ניסיון בפיתוח
הבנה בתרגום דרישות שוק לאיפיון תוכנה/חומרה/מכניקה
ניסיון בכתיבת דרישות טכניות
עדיפות לנסיון בחברות למכשור הדמיה רפואי
המשרה מיועדת לנשים וגברים כאחד.
הבנה בתרגום דרישות שוק לאיפיון תוכנה/חומרה/מכניקה
ניסיון בכתיבת דרישות טכניות
עדיפות לנסיון בחברות למכשור הדמיה רפואי
המשרה מיועדת לנשים וגברים כאחד.
שנות נסיון:3-4 שנים
איזורים:צפון
תחומים:ביורפואה, פיתוח, מחקרים קליניים
היקף המשרה:משרה מלאה
דרוש/ה קצין/ת בטיחות בתעבורה
לפני 27 דקותשלח קורות חייםהוסף לסל
ג'יקובסוןדרוש/ה קצין בטיחות בתעבורה לניהול צי רכב לחברה באזור המרכז.
התפקיד כולל ניהול שוטף של צי הרכב , אחריות על רכבים בחצר לקוח, אחריות על תחום הבטיחות ברכבי החברה, אחריות על ניהול התחזוקה, האחזקה והטיפולים השוטפים, אחריות על הנהגים ונוהגים, עבודה מול מוסכים ,ממשקים פנימיים וחיצוניים.
משרה מלאה.
נא לציין ציפיות שכר!
התפקיד כולל ניהול שוטף של צי הרכב , אחריות על רכבים בחצר לקוח, אחריות על תחום הבטיחות ברכבי החברה, אחריות על ניהול התחזוקה, האחזקה והטיפולים השוטפים, אחריות על הנהגים ונוהגים, עבודה מול מוסכים ,ממשקים פנימיים וחיצוניים.
משרה מלאה.
נא לציין ציפיות שכר!
דרישות התפקיד:תעודת קצין בטיחות בתעבורה- חובה!
רישיון נהיגה A1,C
בעל היתר להפעיל מלגזה עד 20 טון
רישיון נהיגה A1,C
בעל היתר להפעיל מלגזה עד 20 טון
שנות נסיון:1-2 שנים
איזורים:מרכז, שפלה, צפון, דרום
תחומים:קצין בטיחות בתעבורה, קצין רכב, רכב - ניהול
היקף המשרה:משרה מלאה
למשרות נוספות:ג'יקובסון
$ if you Speak GERMAN we want you $
לפני 49 דקותשלח קורות חייםהוסף לסל
- חסוי -You Speak DE? you know how to Sell? so maybe you will make tons of money.
A boutique company base in Herzlia looking for German people that have experience with the financial market.
High salary and high bonuses.
A boutique company base in Herzlia looking for German people that have experience with the financial market.
High salary and high bonuses.
Job Requirements:At least one year of experience in sales.
Ability to work under pressure.
Promotion options.
Ability to work under pressure.
Promotion options.
Required Experience:1-2 שנים
Locations:מרכז, שרון, שפלה, צפון, דרום, יהודה ושומרון
Sub Categories:מכירות בינלאומיות, נציגי מכירות, מנהל מכירות
Job Scopes:משרה מלאה, משרה חלקית
Configuration Control
לפני 53 דקותשלח קורות חייםהוסף לסל
Mazor RoboticsPurpose Statement/General Statement:
• Document control specialist is responsible for managing company documents while also ensuring their accuracy, quality and integrity.
In addition, This position conducts engineering and R&D activities and tasks in support of Change control requirements.
Key Responsibilities & Authorities:
• Maintain configuration control in Engineering documents.
• Responsibility on engineering documentation archive.
• Accompanying and executing engineering change processes in the Company's products.
• Providing solutions to documentation problems at manufacturers and contractors.
• Responsibility for tracking information transfer to the ERP and PLM systems.
• Create new templates for DMR documents such as: DHRs, Drawings, Work instructions, Test procedures, Trainings, etc.…
• Responsible for training employees on records management procedures and policies, which include Engineering documentation.
• Support on-going Engineering change control process
• Management of product DMR including BOM, SOP's, Mechanical & electrical specs.
• Configuration management and Implementation of Engineering Changes/ECO.
• Document control specialist is responsible for managing company documents while also ensuring their accuracy, quality and integrity.
In addition, This position conducts engineering and R&D activities and tasks in support of Change control requirements.
Key Responsibilities & Authorities:
• Maintain configuration control in Engineering documents.
• Responsibility on engineering documentation archive.
• Accompanying and executing engineering change processes in the Company's products.
• Providing solutions to documentation problems at manufacturers and contractors.
• Responsibility for tracking information transfer to the ERP and PLM systems.
• Create new templates for DMR documents such as: DHRs, Drawings, Work instructions, Test procedures, Trainings, etc.…
• Responsible for training employees on records management procedures and policies, which include Engineering documentation.
• Support on-going Engineering change control process
• Management of product DMR including BOM, SOP's, Mechanical & electrical specs.
• Configuration management and Implementation of Engineering Changes/ECO.
Job Requirements:Education:
• BSc. or practical engineer in Engineering Industrial Engineering & Management is preferred.
• Understanding and knowledge of relevant regulations and standards FDA QSR, ISO 13485, ISO 14971, MDD - Advantage
Experience Requirements:
• At least one year proven experience in documentation control of multi-disciplinary products in Manufacturer Factory.
• Experience with Process Validations and qualification of equipment IQ/OQ/PQ - Advantage
• Experience with ECO process optimization/improvement.
Job Specific Skills (Languages, SW, systems, etc.'):
• Excellent communication skills, both verbal and written in English & Hebrew.
• SolidWorks & Office proficient, experience with PDM/PLM systems, Priority.
• being self-directed and ability to work independently.
• being highly-motivated.
• work in a fast-paced and deadline driven environment.
• multitasking skill is required, and in addition ability to stay focused and carry out their tasks in a timely and accurate manner.
• detail-oriented, dependable and trustworthy.
• quick learner and a team player.
Working Relationships:
Internal: R&D departments, QA/RA, Operations and Product
External: Manufacturer, Suppliers, Sub-Contractors.
• BSc. or practical engineer in Engineering Industrial Engineering & Management is preferred.
• Understanding and knowledge of relevant regulations and standards FDA QSR, ISO 13485, ISO 14971, MDD - Advantage
Experience Requirements:
• At least one year proven experience in documentation control of multi-disciplinary products in Manufacturer Factory.
• Experience with Process Validations and qualification of equipment IQ/OQ/PQ - Advantage
• Experience with ECO process optimization/improvement.
Job Specific Skills (Languages, SW, systems, etc.'):
• Excellent communication skills, both verbal and written in English & Hebrew.
• SolidWorks & Office proficient, experience with PDM/PLM systems, Priority.
• being self-directed and ability to work independently.
• being highly-motivated.
• work in a fast-paced and deadline driven environment.
• multitasking skill is required, and in addition ability to stay focused and carry out their tasks in a timely and accurate manner.
• detail-oriented, dependable and trustworthy.
• quick learner and a team player.
Working Relationships:
Internal: R&D departments, QA/RA, Operations and Product
External: Manufacturer, Suppliers, Sub-Contractors.
Required Experience:1-2 שנים
Locations:מרכז, שרון, צפון
Sub Categories:הנדסאים כללי, מהנדסים כללי, מהנדס תעו"נ
Job Scopes:משרה מלאה
More Jobs:Mazor Robotics
Technical Writer
לפני 53 דקותשלח קורות חייםהוסף לסל
Mazor RoboticsPurpose Statement/General Statement:
The Technical Writer creates, develops, plans, writes and edits operational, instructional, maintenance or test procedures for paper, multimedia, web-based publications and user sites; may produce content for embedded user assistance technology.
Key Responsibilities & Authorities:
Conducts interviews with various users and technical staff to gather data for documentation.
Researches and translates technical information into manuals and/or web-based documents for nontechnical and technical users.
May document engineering processes and specifications.
Recommends formats responsive to technical and customer requirements.
Produces products that conform to the company documentation and quality assurance standards.
The majority of time is spent delivering and overseeing the projects – from design to implementation - while and adhering to policies.
Delivers and/or manages projects assigned and works with other stakeholders to achieve desired results.
Coaches and reviews the work of lower level specialists; may manage projects / processes.
to achieve objective, and influence decision-making.
Note: The following are meant to be representative but not necessarily all inclusive of the duties and responsibilities for this position title.
?
The Technical Writer creates, develops, plans, writes and edits operational, instructional, maintenance or test procedures for paper, multimedia, web-based publications and user sites; may produce content for embedded user assistance technology.
Key Responsibilities & Authorities:
Conducts interviews with various users and technical staff to gather data for documentation.
Researches and translates technical information into manuals and/or web-based documents for nontechnical and technical users.
May document engineering processes and specifications.
Recommends formats responsive to technical and customer requirements.
Produces products that conform to the company documentation and quality assurance standards.
The majority of time is spent delivering and overseeing the projects – from design to implementation - while and adhering to policies.
Delivers and/or manages projects assigned and works with other stakeholders to achieve desired results.
Coaches and reviews the work of lower level specialists; may manage projects / processes.
to achieve objective, and influence decision-making.
Note: The following are meant to be representative but not necessarily all inclusive of the duties and responsibilities for this position title.
?
Job Requirements:Required Education, Knowledge and Experience:
Requires advanced knowledge of job area
May have practical knowledge of project management.
Requires a BA
Software and hardware:
• MadCap Flare perpetual license
• MadCap Flare Platinum support license
• MadCap Capture
• Adobe Photoshop
• Adobe Illustrator
• Adobe Framemaker
• Adobe Acrobat DC Pro
• Microsoft Visio
Job Specific Skills (Languages, SW, systems, etc.'):
• Excellent communication skills, written and verbal (Hebrew and English)
• Solid organizational skills including attention to detail and multi-tasking skills
• Strong working knowledge of Microsoft Office
• Works independently under limited supervision to determine and develop approach to solutions
Other Requirements for the role (% of travel, etc.):
Travel may be required. Expecting low intensity
Working Relationships:
Communicates with internal and external customers and vendors.
Requires advanced knowledge of job area
May have practical knowledge of project management.
Requires a BA
Software and hardware:
• MadCap Flare perpetual license
• MadCap Flare Platinum support license
• MadCap Capture
• Adobe Photoshop
• Adobe Illustrator
• Adobe Framemaker
• Adobe Acrobat DC Pro
• Microsoft Visio
Job Specific Skills (Languages, SW, systems, etc.'):
• Excellent communication skills, written and verbal (Hebrew and English)
• Solid organizational skills including attention to detail and multi-tasking skills
• Strong working knowledge of Microsoft Office
• Works independently under limited supervision to determine and develop approach to solutions
Other Requirements for the role (% of travel, etc.):
Travel may be required. Expecting low intensity
Working Relationships:
Communicates with internal and external customers and vendors.
Required Experience:1-2 שנים
Locations:מרכז, שרון, צפון
Sub Categories:כתיבה טכנית
Job Scopes:משרה מלאה
More Jobs:Mazor Robotics
Product Performance Engineer
לפני 54 דקותשלח קורות חייםהוסף לסל
Mazor RoboticsThe Product Performance Engineer effectively monitors post market product performance, conducts product risk evaluations, supports the complaints handling process and performs case clinical analysis to determine cause of failures. Based on clinical knowledge, support complaints handling process and investigations. This position has the responsibility and authority to support robotics surgical systems through the product life cycle, with primary focus in clinical related complaint handling and investigations during post market monitoring. This position also leads cross-functional team to investigate clinical, software, hardware and all other types related complaints.
• Understand the underlying technology of the products.
• Support complaint investigations and clinical analysis in accordance with 21 CFR § 820.198 and ISO 13485:2016 8.2.2
• Develop, prepare, and analyze product performance trend reports
• Communicates results with internal departments, i.e., Product, R&D, RA, and Clinical.
• Provides input from PMS to risk management and CAPA.
• Actively pursue answers and updates from investigation subject matter experts.
Authorities:
• Performs clinical analysis and determines cause of failures
• Preforms post market risk assessment
• Understand the underlying technology of the products.
• Support complaint investigations and clinical analysis in accordance with 21 CFR § 820.198 and ISO 13485:2016 8.2.2
• Develop, prepare, and analyze product performance trend reports
• Communicates results with internal departments, i.e., Product, R&D, RA, and Clinical.
• Provides input from PMS to risk management and CAPA.
• Actively pursue answers and updates from investigation subject matter experts.
Authorities:
• Performs clinical analysis and determines cause of failures
• Preforms post market risk assessment
Job Requirements:Education:
• Bachelor’s degree in scientific area - Must.
Experience Requirements:
2+ years experience working in medical devices industry or similar scientific areas in R&D, PMS or QA functions
Job Specific Skills (Languages, SW, systems, etc
• Excellent verbal and written communication skills (Hebrew and English).
• Office proficient, experience and understanding of ERP, PLM, LMS, Doc Control systems, experience with Salesforce – Preferred.
• Written and verbal communication skills.
• Ability to work with a sense of urgency.
• Orientation to details.
• Able to confidently deal with ambiguous issues and provide input towards suitable actions.
Working Relationships:
• Internal: R&D, RA, QA, Clinical Engineering
• External: Global distributors, Clinical support representatives, Labs
• Bachelor’s degree in scientific area - Must.
Experience Requirements:
2+ years experience working in medical devices industry or similar scientific areas in R&D, PMS or QA functions
Job Specific Skills (Languages, SW, systems, etc
• Excellent verbal and written communication skills (Hebrew and English).
• Office proficient, experience and understanding of ERP, PLM, LMS, Doc Control systems, experience with Salesforce – Preferred.
• Written and verbal communication skills.
• Ability to work with a sense of urgency.
• Orientation to details.
• Able to confidently deal with ambiguous issues and provide input towards suitable actions.
Working Relationships:
• Internal: R&D, RA, QA, Clinical Engineering
• External: Global distributors, Clinical support representatives, Labs
Required Experience:3-4 שנים
Locations:מרכז, שרון, צפון
Sub Categories:ביורפואה, אבטחת איכות
Job Scopes:משרה מלאה
More Jobs:Mazor Robotics
Service Logistic Technician
לפני 54 דקותשלח קורות חייםהוסף לסל
Mazor RoboticsThe goal of this position is to be responsible for daily logistics activities at the Service department.
Key Responsibilities & Authorities:
Ensure RMA & RTV material is receiving/shipping properly, cleaning, storing and distribute as required to meet all relevant demand.
Understand, administer and ensure compliance with all applicable policies and procedures.
Responsible for inventory reliability of the RMA RTV & spare parts warehouses
Ensure workplace health and safety requirements are met.
Key Responsibilities & Authorities:
Ensure RMA & RTV material is receiving/shipping properly, cleaning, storing and distribute as required to meet all relevant demand.
Understand, administer and ensure compliance with all applicable policies and procedures.
Responsible for inventory reliability of the RMA RTV & spare parts warehouses
Ensure workplace health and safety requirements are met.
Job Requirements:Education:
Professional education in warehousing, logistics, manufacturing or any other operational skills.
Experience Requirements:
Medical device or other regulated industry experience is an advantage.
Understanding of RMA, Service processes and procedures – an advantage.
Experience in regulated environments with Quality System requirements.
(Languages, SW, systems, etc.'):
Familiarity with ERP, Priority – Advantage.
Reading, writing English is mandatory.
Professional education in warehousing, logistics, manufacturing or any other operational skills.
Experience Requirements:
Medical device or other regulated industry experience is an advantage.
Understanding of RMA, Service processes and procedures – an advantage.
Experience in regulated environments with Quality System requirements.
(Languages, SW, systems, etc.'):
Familiarity with ERP, Priority – Advantage.
Reading, writing English is mandatory.
Required Experience:1-2 שנים
Locations:מרכז, שרון, צפון
Sub Categories:לוגיסטיקה כללי, תפ"י, מתאם משלוחים
Job Scopes:משרה מלאה
More Jobs:Mazor Robotics
Sr. Medical Safety Specialist
לפני 54 דקותשלח קורות חייםהוסף לסל
Mazor RoboticsThe Sr. Medical Safety (MS) Specialist has primary responsibility to provide medical input across the product lifecycle as an advocate for patient safety and in support of safe and effective use of Mazor Robotics products.
Job Requirements:Bachelor’s degree or higher and RN or MD
5+ years of clinical experience Or Master’s degree and 2+ years of clinical experience.
•Ability to understand & apply practical medical and product knowledge in a competent & consistent manner for Medical Safety activities
•Make competent, risk-based, & timely medical safety decisions
•Understand scientific/technical concepts & function of medical devices
•Experience writing medical reports on complex medical data
•Industry experience in a Medical Device or Pharmaceutical Company, in Safety, Medical Affairs, Drug Information, Clinical Research, Clinical Quality, Regulatory, or related discipline.
Minimum travel required – approximately 10%
5+ years of clinical experience Or Master’s degree and 2+ years of clinical experience.
•Ability to understand & apply practical medical and product knowledge in a competent & consistent manner for Medical Safety activities
•Make competent, risk-based, & timely medical safety decisions
•Understand scientific/technical concepts & function of medical devices
•Experience writing medical reports on complex medical data
•Industry experience in a Medical Device or Pharmaceutical Company, in Safety, Medical Affairs, Drug Information, Clinical Research, Clinical Quality, Regulatory, or related discipline.
Minimum travel required – approximately 10%
Required Experience:5-6 שנים
Locations:מרכז, שרון, צפון
Sub Categories:רופאים/ות, אחים/ות, רפואה כללי
Job Scopes:משרה מלאה
More Jobs:Mazor Robotics
Production Engineer
לפני 54 דקותשלח קורות חייםהוסף לסל
Mazor RoboticsThis position conducts engineering activities and tasks in support of manufacturing requirements.
Key Responsibilities & Authorities:
• Develop design improvements from design freeze and during mass-production.
• Design, qualify, document and validate: assembly & test fixtures/Jigs and tools, release to production and service.
• Performs root causes analysis on equipment and manufacturing process issues.
• Support on-going production processes and equipment, train subcontractors & production line.
• Creating work and testing instructions, production and assembly instructions.
• Provides technical evaluation and implementation plan input to the Corrective Action/Preventive Action (CAPA) program.
• Construction and management of product DMR including BOM, SOP's, Mechanical & electrical specs.
• Configuration management and Implementation of Engineering Changes/ECO.
Key Responsibilities & Authorities:
• Develop design improvements from design freeze and during mass-production.
• Design, qualify, document and validate: assembly & test fixtures/Jigs and tools, release to production and service.
• Performs root causes analysis on equipment and manufacturing process issues.
• Support on-going production processes and equipment, train subcontractors & production line.
• Creating work and testing instructions, production and assembly instructions.
• Provides technical evaluation and implementation plan input to the Corrective Action/Preventive Action (CAPA) program.
• Construction and management of product DMR including BOM, SOP's, Mechanical & electrical specs.
• Configuration management and Implementation of Engineering Changes/ECO.
Job Requirements:Education:
• BSc.in Mechanical Engineering.
• Understanding and knowledge of relevant regulations and standards FDA QSR, ISO 13485, ISO 14971, MDD - Advantage
Experience Requirements:
• At least 2+ years proven experience in design Engineering & manufacturing environments of multi-disciplinary products in Medical Device companies.
• Prior experience with some of the following: complex machined parts, sheet metal Pneumatics, Motors, plastics, cable assemblies, PCBA.
• Experience with design of Jigs, fixtures & Packaging.
• Experience with Process Validations and qualification of equipment IQ/OQ/PQ, pFMEA.
• Experience with process optimization/improvement, lean manufacturing, 5S, Root cause analysis & CAPA.
• Experience with design of surgical tools – Advantage.
Job Specific Skills (Languages, SW, systems, etc.'):
• Excellent communication skills, both verbal and written in English & Hebrew
• Proven working experience with Solidworks – Mandatory.
• Office proficient, experience with PDM/PLM systems, Priority.
Other Requirements for the role ((% of travel, etc.) :
“Hands on”, Independendent, quick learner and a team player.
• BSc.in Mechanical Engineering.
• Understanding and knowledge of relevant regulations and standards FDA QSR, ISO 13485, ISO 14971, MDD - Advantage
Experience Requirements:
• At least 2+ years proven experience in design Engineering & manufacturing environments of multi-disciplinary products in Medical Device companies.
• Prior experience with some of the following: complex machined parts, sheet metal Pneumatics, Motors, plastics, cable assemblies, PCBA.
• Experience with design of Jigs, fixtures & Packaging.
• Experience with Process Validations and qualification of equipment IQ/OQ/PQ, pFMEA.
• Experience with process optimization/improvement, lean manufacturing, 5S, Root cause analysis & CAPA.
• Experience with design of surgical tools – Advantage.
Job Specific Skills (Languages, SW, systems, etc.'):
• Excellent communication skills, both verbal and written in English & Hebrew
• Proven working experience with Solidworks – Mandatory.
• Office proficient, experience with PDM/PLM systems, Priority.
Other Requirements for the role ((% of travel, etc.) :
“Hands on”, Independendent, quick learner and a team player.
Required Experience:3-4 שנים
Locations:מרכז, שרון, צפון
Sub Categories:מהנדס מכונות, תכנן מכאני
Job Scopes:משרה מלאה
More Jobs:Mazor Robotics
דרוש/ה מחסנאי/ת בעל ניסיון בתחום הציוד המשרדי
לפני 56 דקותשלח קורות חייםהוסף לסל
א.וסרמן יבוא ושיווקלחברה המובילה והוותיקה בתחום הציוד משרדי, חומרי יצירה ואומנות
דרוש /ה מחסנאי /ת .
העבודה במשרה מלאה, בימים א'-ה', בין השעות - 8:00-16:30 וימי ו' בין השעות 8:00-12:30.
התפקיד כולל הכנת הזמנות ליקוט הפריטים, קבלת סחורה וסידורה במקום, עזרה בהעמסת הרכבים היוצאים בבוקר לחלוקה.
דרוש /ה מחסנאי /ת .
העבודה במשרה מלאה, בימים א'-ה', בין השעות - 8:00-16:30 וימי ו' בין השעות 8:00-12:30.
התפקיד כולל הכנת הזמנות ליקוט הפריטים, קבלת סחורה וסידורה במקום, עזרה בהעמסת הרכבים היוצאים בבוקר לחלוקה.
דרישות התפקיד:- ניסיון בתחום הציוד המשרדי -חובה !!!
- מגורים חיפה והסביבה הקרובה.
- מגורים חיפה והסביבה הקרובה.
שנות נסיון:3-4 שנים
איזורים:חיפה, קריות, עכו / נהריה
תחומים:מחסנאים, לוגיסטיקה כללי, תפעול
היקף המשרה:משרה מלאה
למשרות נוספות:א.וסרמן יבוא ושיווק
* המשרות באתר מיועדות לכל, ללא הבדל מין וגיל
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