תוצאות חיפוש - Biosense Webster

Innovation, vision, purpose, and social responsibility are the guiding values that make Biosense Webster Inc. (BW) the unique, successful, technology-leading company it is today. Our life-saving technology is used in a wide range of diagnostic and therapeutic medical procedures, improving the quality of care for hundreds of thousands of patients each year in healthcare centers worldwide. A leader in the science and the technology behind the diagnosis and treatment of cardiac arrhythmias, BW pioneered the CARTO® 3 System, an advanced imaging technology that creates real-time, 3D maps of a patient’s cardiac structures, helping electrophysiologists better navigate the heart. Staying true to Johnson & Johnson's Credo and its position as a groundbreaking technology leader in the global marketplace, BW is committed to nurturing a dynamic culture of innovation.

Our Haifa Technology Center (HTC) is a leading innovation center for Johnson & Johnson MedTech. As an innovation hub, it focuses on expanding the capabilities of the CARTO® system and its related catheters. The center works closely with BW’s sister innovation and development center in our technology hub in California. Proactive involvement, entrepreneurial initiatives and out-of-the-box thinking are actively encouraged as part of our culture.

The Head of HR will be responsible for both the Haifa Technology Center (HTC), as well as coordinating the overall HR priorities for Israel in a collaborative setting. The HR leader will partner with local HTC site leadership team to drive the talent agenda and enable business results through capability building, talent management, recruitment, labor relations, total rewards, employee engagement, organizational design, change management, business partnering and social integration in support of business goals. They will address complex organizational challenges by providing HR leadership in support of global business goals, enterprise, and MedTech R&D HR strategies. The Head of HR will be member of the HTC Leadership Team and Management Board, and is responsible for establishing priorities, aligning resources, and leading and mentoring team members as they provide strategic HR support for their respective client organizations.

HTC is a critical technical “HUB” for J&J Medical Tech, as it houses critical capabilities not only for future success of BW. This role will directly report into the Global Head of HR for our Cardiovascular & Specialty Solutions (CSS) Med Tech.

Under and in accordance with all applicable local laws/regulations and Corporate Johnson & Johnson, procedures and guidelines, this position:

General responsibilities:

Enabling growth through creative talent strategies, advancing organizational capabilities, and driving execution through an accountable culture
Demonstrating key HR capabilities in organizational design, leadership planning, career management, performance management, and workforce planning
Drive an innovative, transparent culture through application of organizational development strategies, coaching, talent management, and engagement by crafting “moments that matter” that acknowledges the diversity of our employee needs.
Access and derive insights from talent analytics to inform talent strategies in the development of diverse leadership talent and technical capability across the business
Identify key capabilities aligned with business goals, conducts gap analysis and develops and implements buy/build strategies in partnership with business leaders
Play a consultative role in employee communication in change initiatives within client groups
Enhancing and partnering in leading a clean, healthy, safe, motivating, engaging and indiscriminative work environment.
Responsible for communicating business related issues or opportunities to next management level.


HTC HR Responsibilities:

Support end to end HTC needs – R&D, quality, supply chain, operations, finance, IT, HR, etc.
Develop HR strategy in partnership with CSS R&D HR Head, to drive the achievement of World-Wide strategic objectives in the following areas: Activating our Winning Team, Execution with Excellence, Driving Innovation, and Accelerating Growth.
Clearly outline current and future critical technology capabilities to support future growth
Counseling and support with any HR issues, needs or questions coming from Managers or employees; leading an “open door” policy at Biosense Webster Israel.
Responsible for employee relation issues inquiries including labor relations and ongoing employment issues such as hiring, employment terminations, etc.


Country HR Collaboration Responsibilities:

Ensure ONE HR partnership across the Johnson & Johnson capabilities in Israel to deliver valued solutions for the business and country (e.g. innovative business models and efficiency and effectiveness of current models linked to the business and organizational/talent strategies). This role is the ONE HR Lead for Israel.
Drive the Country cross-Sector HR strategy in alignment with country business strategies and plans, and lead the implementation of processes, programs and policies aligned with Business, HR Business Partner and Shared Services strategies
Lead HR governance for the country, create and direct flexible pool of cross-Sector HR Resources, ensure alignment with Cluster/Regional Sector leads and Global Services.
Drive consistency and change management in global deployment of core processes and program across the country. Establish cadence and rhythm for HR processes with the highest consistency with the global standards across the country.
Develop cross-sector country talent strategy in partnership with stakeholders to grow diverse leadership talent.

• Support R&D Design activities throughout the Product Development process
• Managing Project DHF and providing status to the Project management
• Provide quality inputs for new or modified products development
• Accountable for the Product Risk Management process throughout the PDP
• Support the Design Change process by reviewing the change and performing impact assessments with the team
• Participate and approve the Product Design Reviews
• Review and approval of the Product DHF documents
• Write, review, and implement quality procedures
• Verify the product complies with applicable standards
• Lead quality improvements for product and processes
• Support Internal and External Audits

A Fact: 10% of the older population will suffer from heart rhythm disorder
You can become an expert in the mission of improving their lives!
Design and implement SW components and algorithms for Medical Device products, written in C++ and C# on a multi-threaded system.
This is an exciting opportunity to work with highly talented engineers, working on one of the most cutting-edge technologies.

• Contribute to and help improve CSV processes and practices to maximize the department's productivity
• Considered a subject matter expert (SME) on Q-CSV subject (Quality of Computerized Systems Validation) for GxP computerized systems
• Review and/or approve Change Management forms for GxP CSs
• Work to develop new or improved standard operating procedures and work instructions
• Participate in revision/improvement of procedures and templates governing the Software Development Life Cycle (SDLC) for IT CS
• Provide Quality and Computer System Validation oversight to ensure compliance with regulatory requirements (for example, GxP, Part 11, and Annex 11) and Johnson & Johnson policies and procedures throughout the application life cycle
• Provide independent quality review and approval of validation deliverables and ongoing GxP related change controls
• Confirm validation and SDLC deliverables are outlined in a Compliance/Validation plan and are produced and part of the validation package.
• Partner with global and local IT functions to maintain Computerized Systems Compliance and high level of Data Integrity
• Responsible for Off-the-shelf SW assessment including Supports the assessment process of Off the shelf per FDA 21 CFR 11, as well as supports the validation of customized applications per FDA 21 CFR 11.
• Responsible for GxP automated spreadsheets including spreadsheets assessment support as well as support of the validation of GxP automated spreadsheets.
• Ensure a full compliance with all Company policies, procedures, and guidelines related to Environment, Health & Safety practices
• Establish processes in compliance with applicable international and corporate standards.

In this role you will have the opportunity to take part in the development process of innovative technologies, which improve the quality of care for arrhythmia patients worldwide
We offer you a chance to develop in a challenging role while your studies and a chance to learn and be inspired by professionals in this field.
Key Responsibilities:
In our company, the Automated SW Testing Student role is to ensure that the medical devices and stand-alone software systems, meet their requirements, intended use, and high-quality level.
• Develop, review and execute automated scripts and tools, and document test results
• Perform product testing and defect management throughout the Software Development Lifecycle
• Provide timely and meaningful feedback on the product to the development team
• Plan and design STD documents ensuring that they meet requirements and standards
• Drive innovation; promote knowledge and use of new tools
• Contribute to the company’s team-work and culture

Biosense Webster, Inc., part of the Johnson & Johnson Family of Companies, is a global leader in the science of diagnosing and treating heart rhythm disorders. The company partners with clinicians to develop innovative technologies to improve the quality of care for arrhythmia patients worldwide.

We are looking for a Quality Engineer to join our talented team and support product development processes!

Responsibilities:
• Supports Product Development process compliance; verify that product is being tested per applicable standards and essential requirements are met, and product is properly being transferred to manufacturing and initiate product improvements
• Supports Risk Management methodology and problem investigation
• Reviews Defect Meetings and Clinical Readiness Results and escalate potential Regulatory/Safety
• Supports design controls of class III devices, including Design History File management of the products
• Supports Quality activities during product development, including design changes and assessment and transfer from R&D to production
• Supports and implements quality processes and standards for new product introduction (including internal Johnson & Johnson standards and processes)
• Supports Non-conformances, Corrective and Preventative Actions, Audits, Training and Quality System activities as needed and ensures compliance to all applicable due dates
• Serves as Extended Team Member on Product Development Projects; Leads Quality activities for tools and jigs development

A great opportunity to join the finance department of a Medical Device global leading company, as a finance manager you will lead cross-company processes, work closely with WW Supply Chain and commercial teams, and will be responsible for FP&A, Cost accounting and financial reporting activities.
As a finance manager you will lead the team to provide deep and detailed analysis to create an added value for the business, you will need to provide accurate forecast for local operations and affiliate gross profit, you will provide ongoing support of the operations division in all financial matter and address proper accounting methodology and processes, you will need to work closely with various teams in EMEA, North America and LATAM.

Responsibilities:
• Leading and managing the cost accounting team
• Become the finance partner of Supply Chain teams and Operation business partners – both locally and globally
• Lead the annual business plan and forecasts including affiliate sales, COGS and Affiliates GP for the business and direct inventories.
• Responsibility for the fixed assets management in the company
• Supervise the activities of the cost accounting team and ensure proper implementation as per J&J accounting procedures
• Prepare and maintain inventory reserves analysis
• Work closely with local and global tax departments and support financial annual audit.
• Ensure timely & accurate monthly, quarterly, and year-end period close activities
• Support various projects from financial perspective
• Work closely with various teams around the globe

Biosense Webster, a dynamic and successful company, is looking for a professional, well-organized Executive Assistant to provide support to CFO performing various administrative tasks and supporting them, their departments, and team members. This is an exciting opportunity to establish working relationships with high-level executives and contribute to the overall efficiency of our organization.

The role includes:
• Providing a high level of administrative and operational support in a fast-paced global environment.
• Managing calendars, including appointment scheduling, sending reminders, optimizing, and prioritizing as needed.
• Acting as the primary point of contact for other executives, employees, and external partners.
• Coordinating special global projects within the team, including assistance in the planning and support of on-site and off-site events.
• Participating in Staff meetings, taking minutes during meetings, and following up on action items.
• Making travel and logistic arrangements, working with the travel agency; setting the agenda for business trips, including all documentation; booking meeting rooms, restaurants, etc.
• Preparing and submitting expense reports.
• Scheduling, organizing, and managing department team building activities.

A Fact: 10% of the older population will suffer from heart rhythm disorder.
You can become an expert in the mission of improving their lives!
Design and implement SW components and algorithms for Medical Device products, written in C++ and C# on a multi-threaded system.
This is an exciting opportunity to work with highly talented engineers, working on one of the most cutting-edge technologies.

We are looking for an experienced technical writer for a full time position, responsible for creating technical and regulatory documents in accordance with procedures, Medical Device regulations and requirements.
Work, to be performed both remotely and in our offices with some flexibility, requires standard technical communication services, including technical writing activities, involvement in product development, GUI review, support of translation processes, labeling content awareness, Managing document release through the company’s PLM, etc.

• Provide technical support and maintenance to the production lines and production sites.
• Develop production support systems, testers and tools.
• Investigate and support production issues, customer complaints.
• Lead Proof Of Design activities for HW, SW and process updates.
• Responsibilities include solving technical issues for improving production processes in-house, at BW
• worldwide, affiliates and for subcontractors; reducing company costs by cost reduction project leading,
• reviewing and evaluating production yield;
• On-site support and training
Traveling: expected traveling once a quarter (4 time a year).

Key Responsibilities:
In our company, the SW Testing Engineer’s role is to ensure that the medical devices and stand-alone software systems meet their requirements, intended use, and are high-quality.

Other responsibilities include:
Plan and design STD, STP and STR documents, and ensure that they meet requirements and standards.
Review, execute, and document Software Verification Protocols and test results.
Take part in the Project Development team; Interact with multiple groups within the company: development, clinical, regulatory, quality, documentation, etc.
Support complaint investigation, analyze and identify opportunities for continuous improvement.

This position leads Quality of Class III Product Development to ensure that Company develops its products in compliance with quality assurance system throughout the product lifecycle.
Position includes:
• Leading a team of QA Engineers
• Responsibility for Product Development process compliance with standards and regulations, implementation of methodologies and initiation of improvements
• Leading Risk Management methodology and problem investigation, Reviewing Defect Meetings and Clinical Readiness Results and escalate potential RA/safety issues
• Leading Risk Management processes and activities, as well as design controls of class III devices
• Leading Quality activities during transfer from R&D to production, design changes and assessment
• Supports NC, CAPA, Audits, Training and QS activities as needed and ensures compliance to all applicable due dates

Biosense Webster is looking for a leading Engineering position to leads the Testers & Calibration group; manage the design, development, and production of the test equipment for the company's developed products.

This function will manage the following activities:
• Development and update of testers and calibration systems
• Develop testing methodology for Biosense products
• Life Cycle management of all the systems
• Project management and periodical reporting to Management Board on projects' status
• Suppliers' management – build commercial relations vendors, build agreements and SOWs to support R&D and Life Cycle Management needs
• Lead long term strategy for Testers & Calibration systems in the company aligned with R&D needs, as well as internal and external costumers

We are looking for A Computer Graphics Algorithm Engineer, for designing and implementing Computer Graphics Algorithms for various projects.
This is your exciting opportunity to work with a special team of highly talented engineers. Working with us you'll be exposed to variety of cutting edge technologies and the development of lifesaving products!
In this position you will:
• Design SW components related to computer graphics algorithms for Medical Device products written in C++
• Design and improve computer graphics algorithms based on system requirements
• Develop, implement and evaluate algorithms for new features

A Fact: 10% of the older population will suffer from heart rhythm disorder.
You can become an expert in the mission of improving their lives!
Design and implement 3D SW components and computer graphics algorithms for Medical Device products, written in C++ and C# on a multi-threaded system.
This is an exciting opportunity to work with highly talented engineers, working on one of the most cutting-edge technologies.

Responsible for the development of new products to meet clinical requirements:
• Work with the R&D department throughout all stages of product / project development
• Conduct research and provide solutions to clinical problems
• Performing preclinical tests
• B Testing - Responsibility for site delegates, their guidance and evaluation
• Work with leading physicians throughout the project
• Writing research papers and tutorial presentations

We are looking for a Cloud Architect to join our Digital Platform team that develop cloud solutions that are connected to our medical systems.
The cloud-based system provides the physicians with AI based Big Data analytics tools to improve the EP procedures.
In this role you must demonstrate high professional skills, fast technology adoption, and ability to work on an Azure cloud environment.

Responsibilities:
• Design state of the art cloud solution on the Azure cloud including:
• Managing cloud solution with 100's servers
• Managing Big Data
• Operating and optimizing AI based analysis
• 3D presentation solutions based on GPUs, rendering technology
• Adopting latest Cybersecurity and Privacy technology
• Solution for the clinical needs as presented by our customers (Leading Physicians) and algorithm team
• Explore new technologies and tools to maintain cutting edge solutions
• Guiding the developers with the leading technologies
• Working with partners to define integrated solutions
• Developing the most complex component in the solution
• Being the technology expert is Agile development with emphasis on optimal architect, scalability, performance, Cybersecurity, code quality, and answering regulations.
• Work with Cybersecurity & Privacy team, Regulation and Quality functions to ensure alignment with medical device and data standards.