דרושים R&d Engineering Technician-ultrasound ב-Philips ב-United States, Cambridge

The Bench Service Technician acts as an integral part of AllParts Medical LLC’s operation by ensuring product availability while meeting business targets, executing test and repair requirements and planned activities according to regulatory guidelines, and providing solutions through diagnostics, troubleshooting, and informed repair operations.

Your role:

• Diagnose and repair a variety of multi-OEM High Voltage Tanks & Generators, field replaceable parts including troubleshooting circuits and components, use diagnostic tools and software to assess performance and verify repairs.

• Disassemble and reassemble products with precision, ensuring no damage to internal or external components while working with small tools and delicate components; strong hand-eye coordination required. Complete High Voltage Tanks & Generators testing on multi-OEM diagnostic imaging equipment, utilize structured documentation to complete repair & refurbishment, and discover product repair-capable growth opportunities.

• Accurately document quality assurance records and work orders, including diagnostics, resolutions, test procedures, and case statuses, using the CRM system for knowledge sharing and quality assurance.

• Demonstrates solid technical knowledge, engineering fundamentals, and the ability to work collaboratively, sharing knowledge and experience while solving technical problems independently and making decisions for optimal customer solutions.

• Maintains a strong work ethic and dependability, adapting to new technologies, understanding empowerment areas, and knowing when to escalate appropriately, while taking ownership and accountability for actions, ensuring cost-effective repairs and minimized test and repair time.

the right fit if:

• Minimum 2 years of experience in IT, Network Diagnosis, System Connectivity, Remote Service within Engineering, Medical, or Science related environment or equivalent.

• Your skills include comprehensive PC knowledge, including proficiency with Microsoft Windows and Office applications, along with competence in IT/network diagnosis, system connectivity, and remote service.

• You have at least a high school diploma, vocational education or equivalent.

• You must be able to successfully perform the following minimum Physical, Cognitive and Environmental job requirements with or without accommodation for this .

• Detail-oriented and interested in data management and analytics, exhibiting strong technical knowledge in engineering fundamentals and the ability to solve logical problems independently.

This is an onsite role.

We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help improve the lives of others.

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The pay range for this position in Nashville is $23.87 to $38.19 hourly.

US work authorization is a precondition of employment. The company will not consider candidates who require sponsorship for a work-authorized visa, now or in the future.

Your role:

Provide high-level administrative and secretarial support two R&D senior leaders(software & systems), including managing calendars, travel arrangements, and communications. Collaborate within the global R&D organization to ensure optimal scheduling and efficient operations.

• Assists in organizing workshops, and conferences including preparing necessary materials, ensuring technical setup, overseeing all logistical elements, liaising with senior stakeholder.

• Event Management for award ceremonies, coffee talks, townhalls, hackathons, team events

• Processes expense reports and ensure compliance with organization policies, assists in managing budgets (including travel expenses) and provide financial insights.

• Manage Purchase request and track department expenses

• Communicates local announcements and important updates to and from Executive(s) within the department.

You're the right fit if:

• You’ve acquired 5+ years of experience in comparable executive assistant roles supporting senior leaders for larger teams (up to 350fte) in a multi-disciplinary, multi-site, multi-time zone environment, preferrable for medical product companies

• Your skills include coordinating activities, managing complex agenda’s and using tools like Microsoft Office applications, Ariba, and Concur

• You have a high school diploma or vocational education.

• You must be able to successfully perform the following minimum Physical, Cognitive and Environmental job requirements with or without accommodation for this .

• You have attention to detail, strong organizational skills, computer proficiency and superb communication skills

How we work together

This is an office role requiring minimally 3 days in the Cambridge, MA office.

We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help improve the lives of others.

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The pay range for this position in Massachusetts is $33-53/hr.

US work authorization is a precondition of employment. The company will not consider candidates who require sponsorship for a work-authorized visa, now or in the future.

R&D Development Engineer – Medical Device (Cambridge, MA)

In this role, you will contribute to a breakthrough cardiac ultrasound imaging solution that revolutionizes minimally invasive image-guided therapies for patients undergoing complex life-saving trans-catheter cardiac procedures.

Your role:

• Work on a collaborative, interdisciplinary, and experienced medical device R&D team, tasked with inventing and launching the next generation of products for Philips’ Image Guided Therapies devices business.

• Work on exciting front-end innovation that involves taking ideas and building them into fully functional prototypes. As ideas iterate, translate functional prototypes into production quality applications.

• Design, implement and document clinical-quality software for the R&D and user facing subsystem of a novel intra-cardiac imaging device in a medical-regulated environment with focus on C++ implementation and integration in an Image-guidance system. Experience with Python is also required.

• Participate in software design discussions and code reviews (both internal and multi-functional) for customer centric features and workflows; coordinate with external software contributors, and follow quality & regulatory processes (ISO13485, ISO14971, IEC 62304).

You're the right fit if:

• You’ve acquired 3+ years of professional experience in developing C++ software for medical devices, preferably in medical imaging.

• You have a BS, or MS in Computer Science, Computer Engineering, Electrical Engineering, Software Engineering, or equivalent.

• You are highly skilled in C++, Python and Windows OS, and experienced with common application frameworks and libraries (threading, logging, QT, etc.), and modern dev tools and toolchains (VS Pro, Nuget, CMake, SonarQube, etc.). Experience with toolkits for image-processing and computer vision (OpenCV), and advance visualization (VTK, ITK).

• You must be able to successfully perform the following minimum Physical, Cognitive and Environmental job requirements with or without accommodation for this , including 10% travel.

• Experience in R&D prototyping, hands-on design, development and troubleshooting of user-facing applications, including relevant design patterns and data structures and architectures for distributed applications, and CI/CD pipelines. Experience in translating system and customer needs into requirements and breaking them down into implementable interfaces and building blocks.

How we work together:

This is an office-based role in Cambridge, MA.

We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help improve the lives of others.

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The pay range for this position in MA is $110,000 to $177,000

Additional Information:

• US work authorization is a precondition of employment. The company will not consider candidates who require sponsorship for a work-authorized visa, now or in the future.

• Company relocation benefits will not be provided for this position. For this position, you must reside in or within commuting distance to Cambridge, MA .

Are you interested in an co-op opportunity with Philips? We welcome individuals who are currently pursuing an undergraduate (BS) or masters (MS) degree to participate in 6 month co-op opportunities at our site in Cambridge, MA.

• Provide Mechanical Engineering support for the development of next generation Intra-cardiac Echocardiography (ICE) ultrasound imaging transducers
• Participate in the development of new tooling and mechanical assemblies using SolidWorks
• Set up and execute experimental evaluation of material designs and fabrication processes
• Work alongside a multidiscipline group of engineers ranging from mechanical, electrical, materials, acoustic, system, and software engineers
• Deep-dive into real engineering problems and learn to implement products through the engineering design process (Design-Build-Test-Learn-Repeat)

the right fit if:

• Currently pursuing a Bachelor’s or Master’s degree in mechanical engineering
• A strong team player (Social skills, collaboration, and teamwork are all integral to a successful product)
• Knowledge and understanding of Solidworks (part, assembly, and drawing skillset)
• An independent, self-sufficient, and responsible student

• You must be able to successfully perform the following minimum Physical, Cognitive and Environmental job requirements with or without accommodation for this

How we work together

This is an office role

We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help improve the lives of others.

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The hourly pay range for this position is

Details about our benefits can be found .

US work authorization is a precondition of employment. The company will not consider candidates who require sponsorship for a work-authorized visa, now or in the future.

R&D Application Software Engineer - C++ & Python for Medical Device (Cambridge, MA)

Join the Breakthrough Innovation Teams (BRITE) at Philips to build next-gen surgical robots and bring better care for more people. BRITE is the embodiment of Philips' approach to driving breakthrough innovation by accelerating innovation to nurture nascent projects from early innovation stage to full ability to scale.

Your role:

• Design, develop, deploy, and release software applications in an FDA-regulated environment for a startup-like medical robotics R&D team, tasked with inventing and launching next-generation medical solutions for Philips' Image Guided Therapies business.

• Build, deploy, and maintain production software for ML and data pipelines.

• Contribute to the system and software architecture.

• Provide technical support to the users of the platform.

• Be part of a team in state-of-the-art R&D labs located at the Philips Innovation Campus in Cambridge, MA.

You're the right fit if:

• You have 5+ years of professional experience in software development with exceptional software skills (proficiency in C++ and Python are required). Experience in medical device is required.

• You have knowledge in medical imaging technologies, with a preference for experience in image-guided therapy or surgery and have worked in a regulated software environment, specifically in medical devices.

• Yourprior experience should include SW requirements, containerization (Docker), computer networks,SW architecture design, DevOps (e.g., CI/CD), API design, parallel programming, and object-oriented design.

• You've earned a Bachelor’s Degree, 3+ years with a Master’s degree, or 1+ years with a PhD degree in Computer Science, Computer Engineering, Electrical Engineering, Robotics, Artificial Intelligence, or a related field.

• You must be able to successfully perform the following minimum Physical, Cognitive and Environmental job requirements with or without accommodation for this .

• You will have a competitive advantage if youare familiar with AI deployment and inference technologies like TensorRT and ONNX Runtime.

How we work together:

We believe that we are better together than apart. For our office-based teams, this means working in-person at least 3 days per week. Onsite roles require full-time presence in the company’s facilities. Field roles are most effectively done outside of the company’s main facilities, generally at the customers’ or suppliers’ locations.

This is an office-based role in Cambridge, MA.

We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody, everywhere, has access to the quality of healthcare that we all deserve. Do the work of your life to help improve the lives of others.

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The pay range for this position in MA is $126,000 to $201,000

The actual base pay offered may vary within the posted ranges depending on multiple factors including job-related knowledge/skills, experience, business needs, geographical location, and internal equity.

In addition, other compensation, such as an annual incentive bonus, sales commission or long-term incentives may be offered. Employees are eligible to participate in our comprehensive Philips Total Rewards benefits program, which includes a generous PTO, 401k (up to 7% match), HSA (with company contribution), stock purchase plan, education reimbursement and much more. Details about our benefits can be found .

At Philips, it is not typical for an individual to be hired at or near the top end of the range for their role and compensation decisions are dependent upon the facts and circumstances of each case.

Additional Information:

• US work authorization is a precondition of employment. The company will not consider candidates who require sponsorship for a work-authorized visa, now or in the future.

• Company relocation benefits will not be provided for this position. For this position, you must reside in or within commuting distance to Cambridge, MA .

This requisition is expected to stay active for 45 days but may close earlier if a successful candidate is selected or business necessity dictates. Interested candidates are encouraged to apply as soon as possible to ensure consideration.

R&D Project Manager - Transducer Hardware (Cambridge, MA)

As a technical program/project manager, responsible for End-to-End technical leadership of transducer projects from the project initiation until Market introduction, or internal delivery. Responsible for gaining agreements on and achieving project scope and objectives while balancing schedule, cost, quality to meet product requirements.

Your role:

• Leading Ultrasound transducer development projects through product development milestones and in support of quality improvements, parts obsolescence, assurance of supply strategies, product cost reduction, performance improvements, and new ultrasound features.

• Working with hardware development and program teams distributed across North America and China to lead the planning, definition, specification, design, implementation, integration, and testing of hardware solutions.

• Working with project stakeholders to effectively communicate and review plans, risks, mitigations, metrics, status, variances to plan, and corrective actions.

• Ensuring project execution is in line with project guidelines and directives, meeting goals for scope, quality, schedule, performance, investment, and product cost and driving project to closure.

• Ensuring compliance to corporate and regulatory agency policies/rules/procedures.

You are the right fit if:

• You’ve acquired 7+ years of professional experience with leading complex new product development projects in medical device regulated environment and proven track record of delivering on time and on budget.

• Your skills include product quality and reliability metrics, risk management, and FMEA in medical device regulated environment.

• You have a Bachelor's / Master's Degree in Electrical Engineering, Mechanical Engineering, Biomedical, or equivalent professional experience. PMP Certification is preferred.

• You must be able to successfully perform the following minimum Physical, Cognitive and Environmental job requirements with or without accommodation for this .

• You’re experienced in Project Management, building bottom-up schedules in MS Project, creating detailed budgets and closely monitoring and tracking projects to those schedules and budgets.

• You have demonstrated experience in stakeholder management, thriving in ambiguity and bringing clarity to lead cross-functional teams. Global exposure will aid in the success of this role.

How we work together:

This is an office-based role.

We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help improve the lives of others.

• Learn more about .

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• Learn more about

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The pay range for this position in (Cambridge, MA) is $130,000 to $223,000.00

Additional Information:

• US work authorization is a precondition of employment. The company will not consider candidates who require sponsorship for a work-authorized visa, now or in the future.

• Company relocation benefits will not be provided for this position. For this position, you must reside in or within commuting distance to Cambridge, MA .

You are a part ofthe R&D Systems Engineering organization of the Philips SRC business. As we consider the System Engineer role as a discipline embedded seamlessly into our overall systems engineering workflow, you will work closely with other roles like systems engineers and subject matter experts from the different domains along the development process.

The Systems Engineering team drives the systems elements of R&D development projects, including systems requirement definition and management, architectural definition, control/software/interface product specification and simulation, build integration, system testing and qualification to meet product level requirements.

In addition, you will lead the systems engineering aspects of Model Based Systems Engineering (MBSE). As System Engineering Expert – MBSE you are responsible for the process, method, and tools in the context of model-based system engineering (MBSE) within projects of the Philips businesses globally utilizing the MBSE Modelling tools like Cameo. These projects can cover every phase of the product life cycle, from development, manufacturing, market deployment, operation, and maintenance to phase out. You will also help to deploy capabilities throughout the global company by providing training and coaching to system engineers and system architects.

You will be involved in all system engineering aspects of the Philips V-model, starting with conceptualization, writing requirements, functional and technical design, check & optimize, verification, integration and finally the validation. In your role, you will support system architects and engineers to integrally manage all system engineering aspects in a model-based way supported by the appropriate tools. You will maintain and develop knowledge and expertise, resulting in state-of-the-art approaches to serving our customers.

Responsibilities:

• Incorporates essential operating mechanisms of systems engineering of medical device design and engineering principles and adheres to medical device regulations.

• Defines system requirements, architecture, and interfaces to meet product requirements, risk analysis and industry standards; conducts system design analysis to select key components and defines control methods; and coordinates build and design integration

• Works together to support product verification and validation planning, resolution of technical integration issues, safety agency interface, system testing and coordination and interfaces with Philips design center.

• Conducts design reviews as part of the product development process to ensure customer requirements are met and the designs are manufacture-able, serviceable, and reliable. In addition, it does the same for subsystem requirements and product integration.

As System Engineering Expert – MBSE (Model Based Systems Engineering) you will:

• Lead and support the development of MBSE content in R&D (Research and Development) projects across the business utilizing MBSE modelling tools like Cameo.

• Manage the system engineering information and its traceability (requirements, risks, design decisions, protocols, results) in the model-based system environment of the business

• Create adequate requirements and designs for solutions, products, services, and testers

• Deploy best practices for MBSE globally in Philips to R&D project teams or organizations via training & coaching to enhance maturity

• Identify improvement opportunities in Philips businesses with respect to the MBSE proposition and develop actionable proposals, plans and tailored training materials or workshops to address these

• Manage your activities and services according to good project management practices

• Coordinate small teams of system (MBSE) engineers if applicable

• The ability to make things happen by encouraging and channeling the contributions of others; recognizing and addressing critical issues in a timely manner and acting as an agent for change and continual improvement when required to achieve results.

• Accountability/Ownership: Work closely with team members and take ownership – be a mentor to junior engineers

• Influence: The demonstrated ability to gain acceptance and commitment from others to one’s own beliefs and ideas.

• Negotiating:The ability to construct and maintain a strong bargaining position to ensure positive response and agreement: striving for win-win situations.

• Adaptability:Must possess the ability to understand new concepts quickly and apply them accurately throughout an evolving environment and organize work assignments to meet established timetables.

• Data-driven decision-making: ability to move teams through vague and complex situations. Present complex ideas in a simple manner to resolve issues.

• Relentlessfocus on Quality and Transparencyas an organizational value.

To succeed in this role, you should have the following skills and experience:

• MS or PhD in relevant field including Electrical, Mechanical Engineering, or other related science.

• A minimum of 6 years of experience successfully developing complex medical device (hardware, software, consumables) products for acute care/hospital markets is necessary.

• A minimum of 3 years of hands-on experience (technical) in ventilation is necessary.

• Hands-on experiences in using Model-Based Systems Engineering (MBSE) Tools, of Cameo and similar tools

• Experience with conducting cross-disciplinary feasibility and trade-off studies to evaluate electronic, mechanical, and pneumatic performance from subsystem to system level for issue resolutions

• Analytical and architectural thinking, system view, physical insight, flexibility, and a hands-on mentality to deliver sustainable results and creative solutions.

• Strong understanding of Controls and Software development process, including Model-based Design approach and Test-Driven design methodologies

• Solid understanding of System Verification and Validation test plan/protocols, executing V&V (Verification and Validation) (Verification and Validation) activities, generating, and analyzing test reports

• Understanding of global medical device regulatory environments and clearance processes.

• Effective communication, computer, documentation, presentation, and interpersonal skills are required, as well as the ability to work both independently and as part of a team.

• Maintains strict confidentiality of sensitive information.

We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help the lives of others.
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