careers

Will build clinical and administrative champions, as well as the ability to identify, qualify, and cultivate new opportunities through the entire capital sales process. Will effectively master the clinical, technical, and industry knowledge needed to cultivate and develop surgeon support and engagement, as well as the ability to effectively communicate the clinical, financial, and market development aspects behind the technology/program to the executive team, in order to drive capital sales and meet quarterly and annual sales quotas.

Responsibilities:

·        Ownership of all capital sales initiatives within the assigned geography to meet or exceed quota.

·        Identify, qualify, and cultivate new opportunities through targeting key surgeons, markets, hospitals, ASC’s, developing clinical champions, executing upon the capital sales process through the entire cycle.

·        Create, manage, and grow the capital sales pipeline through targeting, cold-calling, networking with surgeons, executives, industry peers, and leads generated by the company.

·        Effectively present the clinical benefits and the clinical aspects of the technology to prospective surgeons, put clinical validation steps in place, execute upon them, and open up executive discussions around the technology and robotics program.

·        Assist in managing key aspects of the clinical validation steps, including peer to peer discussions, robotic demonstrations, Case Site Visits, Robotic Roadshows, Cadaver Labs, etc.

·        Effectively present the clinical, financial, and market development opportunities behind the technology and program to key hospital and ASC executives in order to secure the program and partnership, on an off-budget timeline.

·        Work with the hospital CFO/Finance Team to tailor the acquisition model that will allow them to capitalize on the technology in an off-budget timeline.

·        Assists potential customers in building their business plans, including hospital-specific market data, competitive market analysis, Return on Investment, and any additional aspects needed to help the customer justify the acquisition of the technology.

·        Develop and assist with market development activities geared towards educating surgeons, patients, and hospital executives on the technology, as well as stimulating the market.

·        Detailed organization and reporting of all key status updates and milestones of the capital pipeline to leadership, via sales reporting tools and processes, pipeline update calls, etc.

·        Leads the launch of new robotic programs, including pre-launch activities with key hospital stakeholders and Memic team members, coordination and execution of the launch meeting, introduction of the Memic launch team, and effective hand-off of the program overall to the Memic clinical and marketing teams.

·        When needed, participates and supports key industry meetings, marketing events, clinical events, etc.

Position Requirements:

·        Bachelor’s degree with a minimum of 5 years demonstrated success in Medical Capital Sales; combination of education and experience is acceptable.

·        Executive selling experience background. (CEO/CFO/COO of hospitals)

·        Ability to travel up to 75%

·        Excellent communication, both written and verbal, required.

·        Prior experience using CRM

·        Valid Driver’s license

We are looking for a smart, self-motivated experienced Advanced Technology Hardware Lead with great interpersonal skills to join our team!

What you will be doing:

You will have an enormous opportunity to make a large impact on the development, architecture design, and implementation of next-generation robotics.

Roles and Responsibilities

• Work with the cross-functional team to understand customer- and support requirements and translate these to technical specifications
• Contribute to the overall system architecture by designing innovative solutions and translating these to design and implementation
• Prototype new designs, test, iterate, and ultimately deliver robust, production-ready code
• Practice test-driven development to achieve the highest code coverage possible for unit testing
• Challenge the status-quo by proposing out-of-the-box solutions and utilizing state-of-the-art technology
• Contribute to the continuous improvement of documentation practices, formal design, and continuous integration/deployment

• Sc. in electrical engineering.
• Expert problem solving, multi-tasking, and prioritization ability.
• Experience with digital circuits, power, and high-speed design
• 5+ years experience in board design.
• Actual practice in a robotic vehicle from end to end – Advantage.
• Hands-on approach.

• Obtain business requirements, formulate functional and technical specifications, and implement these specifications in Netsuite.
• Provide technical and functional best practices in Netsuite with the implementation of some modules such as Order to Cash, Procure to Pay, Billing Etc.
• Provide support, train on system and advise on implementation for Netsuite users
• Support Integration of various technologies into ERP system.
• Participate in all aspects of the application development lifecycle including analysis, design, development, testing, and documentation
• Analyze data modules & identify enhancement and improvement opportunities

• 3+ years of experience working in ERP. Netsuite - an advantage
• Experience in ERP modules such as Procurement, Inventory, Sales and Manufacturing.
• Ability to demonstrate process design/improvement experience
• Experience with translating business requirements to technical design, alongside good analytical skills
• Experience in collaborating and working with different stakeholders
• Hand on knowledge of SuiteScript, JavaScript & SuiteBuilder– an advantage
• BSc in Industrial Engineering – an advantage

Responsible for purchasing, delivery schedule, supplier performance and relationship management of suppliers who deliver components for the manufacturing and R&D.

 Roles and Responsibilities

• Timely creation and distribution of raw materials, components, equipment, tooling, supplies and services Purchase Orders to support NPI and manufacturing activities
• Confirm delivery dates and expedite
• Development and Implementation of cost-saving initiatives
• Ensure that good relations are created and maintained between Memic and suppliers
• Complete Purchasing tasks in accordance with SOP standards
• Participate in MRB session for non-conforming materials and activate timely return of non-conforming materials to vendor
• Prepare monthly metrics for Supplier Scorecards

• Practical engineer or Bachelor's Degree in Mechanical Engineering or other relevant discipline with a focus on purchasing
• 2-3 years’ experience in a purchasing and or planning role within a manufacturing environment (experience in medical device company - advantage)
• Strong knowledge of manufacturing ERP/MRP Systems
• Good computer skills, PLM system
• Good organizational and time management skills
• English communication skills (verbal and written)

Under the direction of the VP, Clinical Affairs, the Clinical Trial Manager will assist in the development and maintenance of the necessary clinical documents to support clinical studies, provide training to study team, coordinate, manage and oversee the various aspects of clinical studies.

Responsibilities

● Assist in development and maintenance of necessary clinical documents (e.g., protocols, design data collection forms, patient consent forms etc.)

● Identify qualified study sites

● Regulatory submissions to IRBs and FDA

● Communicate directly with contracted research organizations (CROs) - Set targets for clinical monitoring team per project goals, oversee and ensure proper monitoring conduct

● Oversee and guide clinical research associates (CRA) and clinical data managers (CDM)

● Coordinating site management activities (training, procedures, technical issues, monitoring)

● Train appropriate clinical research personnel and MEMIC relevant employee on the conduct and requirements of the regulated clinical study

● Support and monitor clinical sites to ensure protocol compliance and data integrity

● Generate study specific work activity reports, and other materials and documents needed for the efficient execution of clinical studies

● Gathering and examining study documents.

● Safety reporting

● Oversee study payments (CRO, site payments etc.)

● Regulatory folder management and maintenance (responsible for the correct filing and archiving of clinical study documents, and the maintenance of study files)

● Collaboration with the IL clinical team

● Complete customer complaints

● Oversee study conduct, and communicating study status to the VP of clinical Affairs on an ongoing basis

● Assuring compliance with CFR and local laws

● Write summaries, presentations, and other supplementary materials for investigator and internal team meetings

● Present clinical data at sales meetings, surgeon meetings and industry conferences

Education and Necessary Skills

● A minimum of a bachelor's degree in life science, Biomedical engineering or closely related field with 5 years of professional experience.

● A minimum of 3 years as a clinical trial manager in the medical device industry

● Excellent organization skills and ability to focus on detail

● Ability to work independently and communicate well with other colleagues

● Outstanding communication skills, both verbal and written

● Time management skills

● The confidence to present protocols or training sessions to colleagues and site staff

● Proficient with Microsoft Office Word and Excel

● Valid driver's license and US Passport required

● Ability to travel 50% domestically and internationally

The Complaints Officer is the backbone of smooth-running system.

Joining Memic, a fast-growing company (FDA Approved, Robotic Surgery focused with multiple installations in the US), as a Complaints Officer, you will lead the initial investigation and assess the ccomplaint appropriateness and correctness.

For the more complicated investigations the officer might need an assistance from the team of experts (R&D people). The rule involves “complaints assessments” which include:

RESPONSIBILITIES

• Initial Investigation
• Interviewing the field team
• Request for the failed device to be returned from the field to recreate the problem encountered - lead or accompany the matter experts (train them) and direct them how to correctly investigate.
• Recreate the problem with equivalent devices
• Request and review the log file
• Summarize the root cause and the conclusions
• Write investigation report
• Follow-up on the immediate correction in field (if needed) - communication with the field (Training, fixing, Etc.)
• Conduct routine checks on systems to avoid failures – preventive actions
• If corrective/ preventive actions needed – CAPA will be opened (responsibility of the QA team)

• Bachelor’s degree in Mechanical/Electrical Engineering, or a related field
• Advanced degrees – an advantage
• +10 years’ system or sustain engineering, experience with multidisciplinary systems (Mechanics and Electronics), invasive medical devices – an advantage, Robotic surgery – a big advantage.
• Proficiency in reports composing (English), including deep understanding regulatory implications of any report.
• Exceptional technical analysis skills (of complex multidisciplinary medical systems)
• Familiarity with risk analysis (failure rates/times)
• Strong attention to detail
• Work well under pressure
• Ability to meet strict deadlines
• Highly responsible and reliable
• Fluent English

The Manufacturing Engineer supports the operations in improving the production process, responsible for correcting missing or wrong functionality and resolving technical issues arising in the products by proposing, testing, and implementing design changes to improve the product reliability and performance.

Roles and Responsibilities

• Continuous improvement of released products by changing the design to improve reliability, manufacturability and cost.
• Non-conformance investigations regarding component failures, finished goods failures, and product returns. Initiate the necessary action to prevent their occurrence and implement changes as required.
• Design jigs and tool to improve manufacturability.
• Develop and implement quality control measures that effectively monitor products.
• Prepare documentation for manufacturing processes (Work Instructions, specifications, routing cards, SOW…)
• Use as technical interface to suppliers.
• Train and qualify new production employees.
• Support risk management activities and risk management reviews on existing products.
• Customer complaints investigation, identification of CAPA’s and report generation.
• Provide support for verification, and validation studies on existing products.
• Support the QA team in conducting audits of supplier quality system and new suppliers’ approval.

• Practical engineer or Bachelor Degree in Mechanical.
•  Minimum of 5 years related experience in manufacturing or assembly processes.
• Previous experience as Manufacturing Engineer (Medical device company - advantage)
• Good organizational and time management skills.
• English communication skills (verbal and written)
• Valid driving license.
•  Good computer skills:
• MS Office SW (Word, Excel, PowerPoint)
• Experience with CAD programs (SolidWorks)
• ERP SW (Priority - advantage)
• PLM system

The Mechanical Assembler assembles subassemblies and products according to work instructions, procedures, mechanical drawings, and other written or verbal instructions.

 Roles and Responsibilities

• Perform all operations related to products production, assembly, and packing
• Perform intermediate assembly tasks such as potting, encapsulating, cleaning, epoxy bonding
• Read work orders, follow production drawings and sample assemblies, or receive verbal instructions regarding duties to be performed
• Performs testing and inspection, using magnifying devices, measuring instruments, and electronic test equipment to ensure parts and assemblies meet production specifications and standards
• Document actions and products by completing required quality and production forms
• Perform all work to meet quality and safety standards and procedures
• Monitor and communicate material needs
• Follow established procedures to avoid contamination of clean-room

• Flexibility and understanding that all staff may be required to perform duties outside their normal area of expertise to meet the mission and goals of the Company
• Experience of minimum 3 years in mechanical assembly processes
• Readiness to work in clean room environment
• Must be able to read, understand and interpret written and/or verbal instructions and have good communication skills in English
• Ability to read and interpret drawings
• Physical ability to stand for long periods
• Valid driving license

The Mobile Showroom Demonstration Specialist fills a pivotal role in support of the Memic Sales and Clinical Services team by 87000ensuring safe and timely transportation of the mobile demonstration lab. The MSDS will be responsible for maintaining the mobile showroom lab inventory as well as maintain proper service records for the vehicle. The MSDS is a technical and clinical expert on the Hominis® system and will assist with surgeon demonstrations, lab sessions, and troubleshooting on an as needed basis. With the provided exposure to training and product demonstrations this position will facilitate movement to other opportunities within the company.

Responsibilities include:

·        Safely transport the mobile showroom lab to and from sites around Eastern US.

·        Support and assist the sales team in the set-up, demonstration and break-down of the Hominis® system.

·        Coordinate closely and effectively with the sales team and marketing team to meet all showroom deadlines and appointments and any marketing related activities such as attendance at Tradeshows.

·        Possess a current and expert level knowledge of the Hominis® system as well as relevant anatomy and procedures.

·        Coordinate with destinations to secure demonstration location for showroom lab.

·        Ensure proper inventory levels of all clinical equipment as well as ensure all equipment is maintained prior to any demonstration.

·        As necessary, work with the clinical and technical services team to provide remote troubleshooting and maintenance assistance.

·        Maintains a positive, friendly, and helpful demeanor, and will represent Memic in a professional manner.

·        Own setup and teardown for clinical demonstrations and lab sessions and provide support during these events as needed.

·        Schedule and document proper maintenance records for the assigned vehicle.

·        Always ensure cleanliness and functionality of the mobile lab.

·        Maintain a clean driving record and obtain all relevant traffic and safety laws.

·        Bachelor’s degree with a minimum of one (1) year prior medical device experience; or an equivalent combination of education and experience.

·        Knowledge of the medical device surgical robotics industry required; gynecology preferred.

·        Current and valid driver’s license with clean driving record required.

·        Ability to travel up to 75% and to independently manage travel logistics and to work nights and weekends as needed.

·        Excellent verbal and written communication skills

·        Problem solver who can maintain composure and identify solutions in a high-pressure environment.

·        Ability to effectively work in an evolving start-up environment where job demands can shift on a regular basis.

·        Self-starter who performs well with autonomy and can be flexible in a dynamic work environment.

·        Evidence of positive and trustworthy relationship-building through all levels of an organization.

·        Ability to lift up to 50 lbs.

The Senior Software Engineer will be responsible for creating a framework and structure to quickly to execute the Company’s priorities to ensure quality products. In this role, the will be responsible for the architect and code of high-quality software, for a surgical robot, according to the clinical, reliability, and performance requirements.

 Responsibilities

• Lead the software architecture design, implementation, documentation, testing, and product release.
• Provide technical knowledge and insight to peers and colleagues and facilitate knowledge sharing.
• Responsible for software verification.
• Ensure integration of the software with monitoring and support tools.
• Review and give constructive feedback on others’ code.
• Ensure the team’s software works well in its operating environment.
• Ensure that the team’s technical product documentation is always complete, accurate and coherent, and maintaining software organization knowledge.
• Ensure troubleshooting and resolution of issues throughout the product life cycle including out of hours support for incident resolution.
• Work with other technical leaders in the broader organization to define, document and distribute best practice and standards.
• Define, lead and encourage continuous improvement of the team delivery and development processes.
• Work with project, product leads to design software and create implementable specifications and tasks at product and roadmap level.
• Work with subcontractors where necessary providing direction, support and documentation.
• Learn new technologies and keep abreast of existing technologies and help introduce them where appropriate.
• Responsible for team’s products archival and release.
• Participate and oversight of software risk assessments.

• Bachelors’ degree in related field required
• Minimum of 10 years’ experience.
• Experience working according to IEC 62304, ISO 14971, IEC/TR 80002-1, AAMI TIR 45
• Skilled in C, C++, C#
• Prior Medical Device industry experience required
• Proven ability to define requirement and design the software architecture.
• Experience collaborating cross-functionally with vendors and internal business partners
• Leadership experience including the ability to quickly build credibility, and influence and/or make decisions across business units

We are expanding our Software Team and seeking a Software Engineering Leader for managing and leading U.S Software Engineering team in the effective design, implementation, and operation of Memic software products and services.

Responsibilities

• Accountable for the design and development of effective software that meets given complex, strategic business needs. 

• Recruit, mentor, and manage an effective software engineering team 

• Ensure alignment of the team products and services with Memic technology and architecture strategy 

• Provide technical knowledge and insight to peers and colleagues 

• Lead the software architecture design, implementation, documentation, testing, and product release.

• Recruit, mentor and manage an effective software engineering team. Provides ongoing coaching and support for the overall success and of the team.

• Provide technical knowledge and insight to peers and colleagues and facilitate knowledge sharing.

• Practice test-driven development methodologies to achieve the highest code coverage possible for unit-testing

• Ensure the team’s approach to testing is fit for purpose 

• Ensure integration of the software with monitoring and support tools 

• Review and give constructive feedback on others’ code 

• Support product and departmental managers in communicating strategy and product fit and effectiveness to stakeholders at all levels 

• Ensure the team’s software works well in its operating environment 

• Ensure that the team’s technical product documentation is always complete, accurate, and coherent.

• Ensure troubleshooting and resolution of issues throughout the product life cycle including out of hours support for incident resolution. 

• Work with other technical leaders in the broader organization to define, document and distribute best practice and standards. 

• Define, lead and encourage continuous improvement of the team delivery and development processes. 

• Work with project, product leads to design software and create implementable specifications and tasks at product and roadmap level. 

• Work with subcontractors where necessary providing direction, support and documentation. 

• Learn new technologies and keep abreast of existing technologies and help introduce them where appropriate.

• Responsible for team’s products archival and release.

• Participate and oversight of software risk assessments.

• Plan and monitor work plans, coordinate, develop, document, and maintain robust and extensible software.

·        Bachelors’ degree in Computer Science or Engineering with a minimum of 7 years hands-on software development experience (C++/C#)

·        Minimum of 2 years’ experience managing and developing a team of Software Engineers or Developers

·        5+ years of experience in software medical device development classified as Class 2 and/or Class 3 medical device

·        Fluent in real-time systems and object-oriented languages, Cloud advantage

·        Experience in motion control and Robotics Advantage

·        Expertise with real time SW and communication protocols

·        Demonstrated applied expertise in FDA design control requirements (21 CFR 820.30) as applied to medical device software and medical device regulations including ISO 13485, ISO 14971, Cybersecurity, IEC 62366, and IEC 62304

·        Experience in working in an environment following Agile methodology – advantage

·        Demonstrated applied expertise with Software FMEA process

·        Experience leading nearshore and/or offshore development partners

·        Familiarity with health and data privacy regulations

·        Ability to travel domestically and internationally 10%.

·        Valid US Passport

We are looking for a passionate and ambitious hands-on Software Team Leader to join our Software group.

Responsibilities:

• Managing an experience Software engineers
• Taking part of architecture design and implementation
• Execute full software development life cycle (SDLC)
• Review and give constructive feedback on others’ code
• Work with other technical leaders in the broader organization to define, document, and distribute best practices and standards
• Plan and monitor work plans, coordinate, develop, document, and maintain robust and extensible software.

• Bachelor’s degree or global equivalent in Engineering or Computer Sciences.
• 40% hands-on
• Minimum of five years of experience in software development.
• Experienced with real-time multidisciplinary systems
• Experienced with SOA application design
• Experienced with complex software architectures   

Advantage:

• Experienced with .Net development
• Experienced with Medical device development

About Memic

Memic has set out to transform robotic-assisted surgery, with proprietary technology that has the potential to far surpass today’s best solutions. Providing unprecedented access and maneuverability, our Memic’s Hominis® surgical platform features miniature, humanoid-shaped robotic arms with human dexterity, superhuman flexibility, and 360˚ articulation. In addition to these features, the system will be sold at a significantly lower price compared to other marketed robotic surgery systems potentially allowing more medical facilities including hospitals and ambulatory surgical centers to access and adopt surgical robotics. Beyond the current applications for transvaginal procedures, Memic is further developing this technology to explore use in abdominal single and multi-port surgery, as well as other transluminal indications.

Note: The following are meant to be representative but not necessarily all inclusive of the duties and responsibilities for this position title.

Core Job Responsibilities

We offer you a position where you would be:

●      Providing technical leadership and oversight of diverse, distributed teams of engineers in development of complex medical device HW, and SW from concept to release

●      Translating customer unmet needs into actionable UI/UX and system technical requirements, supporting platform architectures, and associated project execution plans

●      Translating technical results into easily understood recommendations that will influence senior stakeholders

●      Work across multidisciplinary teams to create, verify, manage, and track system- and subsystem-levels of requirements and specifications

●      Demonstrating leadership and advanced knowledge of SW, HW and electronics development methodology (Waterfall, Agile, interactive etc’)

●      Plan and oversee tasks breakdown and execution within the relevant design teams and designated projects and account for the project development execution in quality on time

●      Work with development teams to support risk analysis, design FMEA, and identify proper risk mitigation solutions to the complex robotic surgical system and subsystems

●      Provide technical leadership in system integration, testing, verification, problem solving and product improvements

●      Oversee and be deeply acquainted with development processes regulated by relevant standards – Risks, usability etc. Ensuring systems design and documentation complies

●      Hands-on work on system HW components and SW when developing new capabilities and features

●      Attend R&D labs and surgeries observation for in-depth clinical knowledge

●      Work closely with relevant stakeholders: PMO, Product, Clinical, Service, QA, DA etc.

●      Support key processes in the development life cycle, such as: sustainability investigations, SW and HW optimization, technical experiments, Risk management, usability validation and UI/UX specifications

Qualifications

Note: The following are meant to be representative but not necessarily all inclusive of the duties and responsibilities for this position title.

Must Haves

●      B.Sc or M.Sc from a known institute in the fields of: Biomedical/electrical/Software/robotics/algorithms System engineering

●      Experience through full product development cycle of complex medical device systems, or other regulated fields, from initial concept to release to market  

●      Demonstrated technical leadership and ownership

●      Proven ability of analytical problem solving, troubleshooting and issues investigations

●      Ability to provide guidance and direction to less experienced technical personnel

●      Track record of strong cross-functional collaboration, influence, and management capabilities enabling highly effective project teams         

●      Self-driven, Can-Do attitude (a kick-starter)

●      2+ years of work experience as system eng. in medical devices or other highly regulated industries

●      3+ years of hands-on technical\+ development experience on either Electrical/ SW/ Biomedical/ robotics

●      Great team player with engagement creation skills

●      Fluent in technical english – verbal & written 

●      Ability for travel up to 20% of the time

●      Driver’s license

Nice to Haves/Advantage

●      System engineering of a complex medical device experience – Big advantage

●      Experience in Electro-surgery - Big advantage

●      Development experience in a regulated environment – advantage

●      SW/HW/electronics/Algo characterization and requirements writing – big advantage

●      System performance modeling, simulation, and test (python, Matlab…)

●      Global company experience - advantage

Image processing background - advantage

Energetic and passionate Technical Service / Quality Engineer with an entrepreneurial spirit and strong technical writing and communication skills who will support Quality activities of the Technical Services Engineering team. Support process in compliance with ISO 13485 and FDA 21 CFR 820 Quality Systems Regulation. Work with Technical Services and Quality Assurance teams to implement and support processes.

·        Work with SMEs to author and edit Quality Management System (QMS) processes as required

·        Participate in Feedback process (field service reports, clinical case reports, customer satisfaction surveys, etc.) and ensure proper documentation.

·        Support the documentation and review of service work orders (Service Records, Customer feedback tickets, etc.) and activities for QA compliance and disposition.

·        Ensure proper handling & closure of support and commercialization related CAPAs incl. task tracking, root-cause analysis, and completion of documentation.

·        Support and provide input to continuous improvement process resulting from lessons learned.

·        Travel to and participate in service calls, installations, and cadaver labs as necessary to maintain practical field service process knowledge.

·        Ensure Service tooling is calibrated and maintained in accordance with SOPs.

·        Support achievement of quality objectives and requirements by working with the cross-functional team

·        Assist with the implementation, validation, and maintenance of software systems, including but not limited to: Service Management Software (SMS), Customer Relationship Management (CRM), Complaint, Training, etc.

·        Support documentation of logbooks as needed for Quality Records, such as Feedback, Complaints, CAPAs, Training, etc.

·        Support external audits through back-room documentation retrieval and SME prep, or front room scribe duties.

·        Facilitate and support quality and engineering in the investigation and resolution of complaints.

·        Support maintenance of training records for Employees and Customers

·        Support overall cross-functional compliance to Good Documentation Practices (GDP) & Good Manufacturing Practices (GMP).

• Bachelor’s degree or equivalent in an engineering field, or current enrollment in a Bachelor’s of Engineering program.

• Experience in the medical device industry an asset.

• Familiarity with ISO 13485 and FDA 21 CFR 820

• Strong technical writing and communication skills

• Strong organizational and project management skills

• An appreciation for the documentation supporting successful process execution

Computer and edge equipment technician operates multimedia equipment, HD

• Work as a computer technician
• Working in collaboration with external suppliers including contact, escalation and operation
• Responsibility for installation, maintenance and management of computers, telephony and audio-visual equipment
• Technical support for computing equipment, end equipment, projector, smart boards, scanners, printers and more
• Technical support for professional staff and their training combined with useful computerization in their work
• Technical support for the operation and use of software
• Execution of any task directed by the direct supervisor

• Computer technician or computer practical engineer or holder of a certification certificate for the maintenance of computers and / or communication networks from a recognized institution for at least 150 hours.
• Proven experience with multimedia equipment (smart screens, conference rooms) from the companies Logitech and Cisco.
• Proven knowledge and experience of at least 3 years in locating, handling and repairing hardware and software problems, controlling installations and troubleshooting Microsoft Windows and Office software.
• Graduate of Microsoft Computer Network Management Course - an advantage.
• MCSA certification, A + - a significant advantage.
• 
  

Additional requirements:

• Hebrew - Fluent
• English - High level

Additional talents:

• Good interpersonal communication, orientation and service.
• Has the ability to express himself in writing and speaking in Hebrew / English at a high level.
• Ability to organize and plan tasks with meticulousness and accuracy and ability to meet deadlines.
• Willingness to work beyond normal hours and at short notice in response to exceptional cases.
• Work documentation and LLD performance prior to assignment

We are looking for a skilled V&V Engineer to design and implement test procedures for our robotic systems.

Gain in-depth knowledge in system requirements, system architecture, and features and work with all R&D disciplines.

Roles and Responsibilities

• Design system testing to verify the design output
• Draft testing protocols and reports
• Lead testing projects under design control procedure
• System Bench Testing development
• System integration testing
• Fixtures development and qualification
• Perform basic statistical analysis on collected data and present results
• Execute test cases in accordance with system test plans to ensure product compliance with applicable standards.
• Work according to the full product lifecycle including design, testing, documentation and ECOs implementation.

• Bachelor’s Degree in an engineering discipline
• At least 4 years of experience in the medical device industry (multidisciplinary products - advantage)
• Experience in system R&D and system verification teams
• Familiarity with Sterilization validation, biocompatibility testing – Advantage
• Knowledge of testing methodologies
• Experience in testing according to medical standards - an advantage
• Multitasker, responsible, hands-on approach
• Ability to work within tight deadlines
• High communication skills (written and interpersonal)
• Fluent English
• The position is full-time