דרושים System Architect ב-Philips ב-India, Pune

• Analyzes and troubleshoots testing failures, documenting them in the anomaly database, initiating corrective actions as necessary and ensuring respect for established protocols, working under general supervision.
• Executes targeted development assignments within the defined scope, complies with working agreements with teams, making timely and effective decisions to achieve closure on work items.
• Synthesizes proven approaches and integrates multiple strategies to solve complex problems or optimize solutions in product designs and manufacturing processes.
• Develops and implements new product designs and design improvements for instrumentation in the medical device field, ensuring alignment with customer requirements.
• Participates in the technical development of a Continuous Integration and Continuous Deployment framework for multiple initiatives, ensuring process optimization and efficiency.
• Conducts preliminary studies and modifies subsystem designs to address complex problems, deriving specifications from customer requirements and ensuring adherence to regulatory standards and company quality systems..
• Collaborates with engineers to devise integration phases, criteria, and tests, assists in the designing of features for digitally-assisted medical solutions and supports installation, integration, and monitoring of external clinical sites.
• Keeps abreast of developments within the field, exchanges information effectively to promote cross-functional collaboration, interacts with stakeholders to ensure alignment on project goals and timelines.
• Conducts experimental activities related to test project outcomes, analyzes data, and evaluates results to inform decision-making and implementation of improvements.

• Specify image chain requirements as part of a development project and Test and verify image chain component (Generator, Tube, Collimator, Detector, Monitor etc) against the requirement
• Be responsible for integrating image chain components, adjustment & calibration and verifying the system with respect to meeting the safety, functional, performance and reliability.
• Be responsible for selection of image chain components and subsystems to achieve target cost and image quality.
• Be responsible for detailed technical design for the components including DFMEA, Risk assessment.
• Lifecycle management of image chain components including obsolescence management.
• Collaborate with cross-functional/cross regional teams to release design changes and customer support
• Align with supplier on the requirements and design aspect to ensure products quality.
• Evaluate New and competitive technology for image chain subcomponents.
• Good team player with ability to work independently and act pro-actively.

Minimum required Education:

• Electrical/ Electronic/Biomedical background (B.Tech/M.tech) with 8+ years’ experience
• Solid experience with Power electronics and electronics product design and development
• Analog and Digital circuit design. familiar with Operational amplifiers, Inverter design ( SiC technology) , H- bridge design , Power transformers design
• Understanding X-ray Physics, having Generator, Tube, Collimator, Detector or Monitor knowledge is plus
• Strong understanding of Medical QMS and lifecycle management processes.
• Strong Communication skills: Ability to present technical data/concepts concisely and effectively to various audiences/stakeholders
• Understanding medical standards like IEC 60601-1, IEC 60601-1-3, IEC 60601-2-54
• Detailed/ Structured documentation practices and decision making
• Analytical/Fact Based/Logical problem solver

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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If you’re interested in this role and have many, but not all, of the experiences needed, we encourage you to apply. You may still be the right candidate for this or other opportunities at Philips. Learn more about our culture of impact with care .

Test and Verification Engineer

Be part of a multidisciplinary team of highly skilled technical specialists working on innovative (automated) test solution projects. These projects can cover every phase of the product life cycle, from development, manufacturing (manufacturing test development, fitness for use, MSA’s) and maintenance. In your role, you will work with together with Test architects, the SW architects (automation) and other T&V Engineers from within our own organization as well as from our customers organization.

You are responsible for

• Software Development for ATE(Automated Test Equipment), test setup, tools in the technologies like LabVIEW, Test Stand, MATLAB, Python language
• Designs, develops, evaluates, and conducts integration, testing, and verification activities of (elements of) products with focus on electrical, electronics, mechatronics and (embedded) software aspects and concludes this with formal reporting.
• Developing, executing, and documenting test protocols (for elements, (sub)system integration, functional and non-functional tests) against the test requirements by using established test methods, techniques and tools.
• Take ownership on developing and conducting tests to verify functionality (performance, reliability, safety, security, compliance) and formally reporting the results.
• Analyzing and post-processing of measurement data by using statistical techniques (Minitab) and providing technical documentation in compliance with internal procedures and regulations/ standards applicable (e.g. according to ISO 13485, ISO 17025 21CR820 and GDP, IEC 60335)
• Prepare test documents, technical reports, presentations, as required.
• Setting up and maintaining both large and small scale device testing

To succeed in this role, we are looking for a System Test & Verification Engineer with following characteristics:

• Batchelor’s or Masters degree in electronics, Electrical, mechatronics engineering
• 4 - 6 years of experience in R&D area or manufacturing (design engineering, test development, manufacturing, quality assurance or research) Good understanding of product development and or design verification process of industrial products, medical business is plus
• 3+ years of experience in System/Product test automation , test designing, executing, reporting and excellent documentation skills.
• Experience in LabVIEW, Test Stand, HIL, MIL, MATLAB, Python / Arduino, scripting languages
• Experience in using test & measurement hardware like Function Generator, Multimeter and power supplies, Industrial Sensors and transducer etc.
• Knowledge of Advanced LabVIEW software architecture development skills.
• Working Experience in Industrial automation protocols like Ethernet, UDP, TCPIP, RS232, RS485, MODBUS, OPC Server, CAN, LIN, I2C.
• Working experience on NI Hardware like cDAQ, cRIO.is plus
• Professional in Execution of detail test plan from system to component level in the domain of functional Performance, Reliability, and compliance
• Good at applying concepts and implementing in test and verification field.
• Structured approach in planning, test execution and defect identification and closure.
• Knowledge of medical device regulations and standards (e.g., IEC 60601-1, EU-MDR, FDA cGMP) is plus
• Exposure on Requirements analysis, Traceability Matrix and Risk Management
• Affinity with Systems engineering and Requirement engineering is plus
• Open to travel at different sites on an occasional basis
• Excellent working with others with a strong sense of teamwork and collaboration
• Strong desire to learn and adapt to new technologies and challenges
• Good communication skills analytical thinking, physical insight, continuous learning mindset

Good to have

• Knowledge of Machine Vision strategies.
• Knowledge to understand electric wiring diagram Participating in the development of verification test plans for HW and SW domain.
• Understanding of embedded architecture and hardware interfaces

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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Job Description

, you are responsible for the development and maintenance of X-ray generators. Together with a multidisciplinary team of engineers, you play a crucial role in getting the X-ray generators to the required performance, by owning the design, development, testing, and maintenance of embedded systems and safety/mission critical embedded software and firmware, that control various functions of X-ray generators.

You are responsible for:

• Requirements, design, implementation, test and integration of module/sub-system in accordance with the higher-level architectural requirements and design specifications
• Ensuring that the design is consistent with the higher-level architecture and requirements
• Ensuring that the proposed design would have the safety, reliability and quality features built-in
• Responsible for ensuring that the design meets the performance, quality and cost criteria
• Conduct concept and feasibility studies. Leads the introduction of new technologies
• Ensuring that there is proper documentation per standards for the developed design
• Ensuring the mutual consistency and efficient integration of the separate components in modular design that meets the product specification
• Ensuring that his design modules meet the product certification requirements
• Drawing up personal schedule and reports on progress
• Defining and assessing the Work Breakdown Structure/planning/costs of his/her area
• Being abreast of technical developments in own field through study of literature and technical contacts
• Mentoring/guiding/hand-holding young engineers in the team and helping them ramp-up well
• Maintaining product and company reputation by complying with country specific regulations

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

• Completed engineering studies at University level; BE/BTech/ME/M-Tech in Electronics or Electrical Engineering, with 12 to 15 years of experience
• Experience in complete life-cycle management of embedded software, preferably for medical products
• Expert in C, C++ and other embedded programming languages
• Proficient in hardware description languages like VHDL, Verilog etc.
• Knowledge of Software Design Life Cycle (SDLC)
• Good knowledge of modern OS coding techniques, IP protocols and hardware interfaces
• Experience in 16/32-bit microcontroller-based design and programmable devices (FPGA/CPLD/SoC etc.) and their interface
• Knowledge of communication interfaces like RS232, RS485, CAN, EtherCAT, Ethernet and USB
• Hands-on experience in developing control software for close-loop systems.
• Hands-on experience in using simulation and implementation tools such as MATLAB and SIMULINK
• Excellent debugging skills - ability to understand and debug problems across hardware/software boundaries
• Experience in printed circuit board bring up and testing
• Knowledge of software tests and static code analyses
• Knowledge of firmware development environments such as IAR or Eclipse as well as version control systems like GIT
• Should have experience in DFMEA and design of Fail-Safe Systems and Sub Systems
• Knowledge of IEC 60601 standards will be an added advantage
• Knowledge of Global Medical Quality and Regulatory Standards e.g. IEC, FDA, UL, CE, CSA etc.
• Hands-on experience with tools like Agile, Clear-quest, Windchill or equivalent
• Disciplined team worker, ability to work independently
• Result oriented team player
• Ability to present and articulate ideas to key stakeholders and leadership team
• Excellent communication skills and Positive ‘can do’ attitude
• Quality mindset in design and documentation
• Global and Cross-functional Experience/Skills in a Matrix Organization will be an added advantage.

Onsite roles require full-time presence in the company’s facilities.Indicate if this role is an office/field/onsite role.
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• BE/BTech/ME/MTech with 10-15years of experience in Software architecture, design and development in embedded software/firmware using C and C++ is required
• Experience in software development in medical industry; experience with IEC 62304, FDA guidance for medical device development and other relevant medical device regulatory standards is highly preferred
• Experience with RTOS (MUST) and BareMetal based Embedded Software. Preferred knowledge in Linux Environment
• Microprocessor development Hands on Knowledge of System - (domain knowledge for designs SW, HW, Mech system)
• Experience with Platform initialization, Board support package integration, low level drivers for peripherals such as PCIe, I2C, eMMC, SPI, USB, UARTs as well as Memory Management, Scheduling, Interrupts and multi-threading
• Aware of SDLC. Good grasp of Design Patterns/ Multithreading, Code Reviews
• Experience in Agile SW Development practices; experience in scaled agile framework (SAFe) is preferred

• Technical Documentation
• Agile Methodology
• Software Development Life Cycle (SDLC)
• Business Acumen
• Strategic Planning
• Escalation Management
• Systems Integration
• Quality Specifications
• Software Architectures
• Stakeholder Management
• Resource Planning & Allocation
• Software Design
• Code Reviews
• Requirements Management
• Regulatory Requirements

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.
• Learn more about .
• Discover .
• Learn more about .
If you’re interested in this role and have many, but not all, of the experiences needed, we encourage you to apply. You may still be the right candidate for this or other opportunities at Philips. Learn more about our culture of impact with care .

Your challenge

As Test and Verification Architect you are responsible for the realization and management of Product testing and verification in product creation and its lifecycle maintenance projects. These projects can cover every phase of the product life cycle, from development, manufacturing, market deployment, operation and maintenance to phase.

You will be mainly involved in develop and implement test strategies, design for testability (DFT), Design for manufacturing test (DfMT) guidelines for systems ,subsystems ,parts , PCBA designs. Additionally, the definition and review of testable requirements and the development of an optimization, integration, and testing strategy towards product realization.

In your role, you will support system architects to integrally manage the design, development, execution and reporting of tests. You will maintain and develop knowledge and expertise resulting in state-of-the-art approaches to serve our customers with the test and verification service proposition.

You will help to deploy best practices throughout the global company by providing training and coaching to development engineers and system architects.

You are responsible for

• The management and realization of product test and verification in R&D projects and projects covering life cycle maintenance of product across the businesses.

• Integrally manage the design, development, execution and reporting of all test and verification engineering activities.

• Defining and reviewing testable requirements and the development of an optimization, integration and testing strategy ,Test Methodology ,Test protocols towards product realization.

• Support project leaders, system architects and lead engineers to develop a risk-based integration and testing strategy

• Review of (quality of) Design verification documentation, FMEAs, Risk Assessments and being able to perform gap analysis with respect to standards and regulations.

• Create, supervise and/or review test protocols

• Create actionable integration and verification plans to release products and processes according to specified requirements.

• Prepare and set up the test base in line with the project plan.

• Take ownership for test execution, sample management and test reporting.

• Liaise with test centers, lab facilities to execute the verification plan.

• Develop and implement design for testability (DFT),Design for manufacturing test (DfMT) guidelines and ensure guidelines are followed throughout the design process.

• Develop and implement test strategies, Define testability metrics for PCBA designs.

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

• Coordinate small teams of test & verification engineers if applicable.

• Deploy best practices for risk and test and verification management 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 Test and Verification proposition and develop actionable proposals and plans to address these.

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

• Master or Bachelor’s degree in Electronics/ E&TC /Electrical Engineering

• Around 15 yrs. of experience with a minimum 8 years of experience as a Test and Verificationlead/architectin an industrial product R&D environment.

• Experience working in a regulated environment or a medical device company has a strong preference

• In-depth knowledge and a proven track record in implementing and applying concepts in test and verification and test management field.

• Experience in risk-based test strategy development and implementation.

• Experience with functional tester developments for systems, modules ,PCBA and Components.

• Experience in DFT guidelines, Test Coverage and test methodologies.

• DfSS green Belt or equal by experience and manufacturing quality control knowledge.

• Experience / ability to design-develop, test and debug Test automation applications.

• Experience in Test automation using Python , Labview , other platforms /tools is plus

• Good understanding of PCBA mfg process and in-process control techniques is plus

• Good understanding of commercially available PCBA test techniques is plus

• Working Experience in Industrial automation protocols is plus

• You combine analytical and architectural thinking, physical insight, a continuous learning mindset and ability to create structure that leads to deliver sustainable results and creative solutions.

• Strong communication skills, gathering relevant information, bringing strategies to results of teams and convincing various stakeholders.

• Excellent reporting and documentation skills.

• Good project management skills.

Furthermore to be successful in this role you are :

• Motivated, self-driven with a determination to succeed and the ability to adapt to change.

• Analytical, you are open to new ideas and believe in continuous learning in order to develop new competencies.

• A critical but constructive reviewer

• Customer focused, have excellent communication skills and you are a team player.

• Leadership: Provides guidance and enables development in own team. Mentors junior staff within own team.

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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You will be responsible for driving meaningful and innovative product development, generating ideas/concepts in feature development to improve quality and reduce cost, as well as performing the role of a technical lead in taking the product development through manufacturing release while transferring products between suppliers and manage sustaining of different devices by following PDLM/MLD process.

To be part of an exciting team and contribute to the design, development and maintenance of Diagnostic Imaging (MRI, CT/AMI, DXR etc.) components and products. In this role of Mechanical System Designer, you are responsible for the development and maintenance of Image Acquisition Platform (IAP) - Hardware Systems/Subsystems and will gain substantial knowledge of complex systems in medical imaging environment. Together with a multidisciplinary team of engineers, you play a crucial role in getting these systems/sub-systems to the required performance, by understanding the electrical, electronics and controls and looking for the best solutions within those boundaries. This requires broad orientation, conceptual skills and a “can do” mentality, keeping abreast with all trends

Your role:

• Leading the development and release of system/ electro-mechanical modules or reverse engineer existing products to improve overall long-term system quality, reliability, yield rates, and cost effectiveness.
• Working with a cross-functional team to ensure the design and development of electromechanical components to meet the needs of the internal and external customers.
• Working with design partners/suppliers and lead product development activities from design concept to manufacturing release.
• Using modelling and simulation tools to create and modify architectures, 3D designs, and 2D drawings.
• Drive continuous improvement projects related to design implementation, manufacturing process, product quality and reliability.
• Requirements, design, implementation, test and integration of module/sub-system in accordance with the higher-level architectural requirements and design specifications
• Ensuring that the design is consistent with the higher-level architecture and requirements
• Ensuring that the proposed design would have the safety, reliability and quality features built-in
• Responsible for ensuring that the design meets the performance, quality and cost criteria
• Conduct concept and feasibility studies. Leads the introduction of new technologies
• Ensuring that there is proper documentation per standards for the developed design
• Ensuring the mutual consistency and efficient integration of the separate components in modular design that meets the product specification
• Ensuring that his design modules meet the product certification requirements
• Drawing up personal schedule and reports on progress
• Defining and assessing the Work Breakdown Structure/planning/costs of his/her area
• Being abreast of technical developments in own field through study of literature and technical contacts
• Maintaining product and company reputation by complying with country specific regulations
• Supplier evaluation and communication

You're the right fit if you have :

• M.Tech / B.E/ B.Tech in Mechanical/ Electrical/ Electronics or Equivalent Engineering
• 10+ years of relevant experience in design & development of electro-mechanical subsystems & systems.
• Strong communication and collaborative abilities proactively seeks out expertise and advice and input from others in a collaborative team-environment.
• Experience in developing the requirements for electro-mechanical assemblies.
• Knowledge in part qualification and statistical process studies such as CP and CPK and be able to work with suppliers to improve part process capability.
• Experience in lifecycle testing and verification activities of cables to meet functional and lifecycle requirements.
• Experience working with suppliers and design partners, including part/module development and resolving technical issues.
• Strong technical writing/ documentation skills for regulated medical device design environment, including requirements definition.
• Knowledge of good design practices and experienced with DFMEA.
• Knowledge of EMI/EMC standards and testing for conformance • Knowledge of mechanical design compatibility aspects
• Knowledge of IEC 60601 standards will be an added advantage
• Knowledge of Embedded Software Programming will be an added advantage
• Ability to understand and debug problems across hardware/software boundaries
• Knowledge of Global Medical Quality and Regulatory Standards e.g. IEC, FDA, UL, CE, CSA etc.
• Demonstrated ability to effectively work with cross-functional stakeholders to ensure the design meets their expectations and needs, and that the needs/requirements are properly documented.
• Experience with document control systems (E-Matrix, Agile) and FDA/ISO regulated medical device design environment.

Onsite roles require full-time presence in the company’s facilities.
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System Architect

design, develop and maintain CT/AMI (Computed Tomography / Advanced Molecular Imaging) products and solutions. This opening is for India Product Engineering group of CT/AMI at HIC Pune.

Your role:

• Carrying out all System Engineering activities of assigned product(s)/product line(s) as per the global system engineering process
• Analyze product(s) issues from the field (post market) and take complete ownership in providing relevant solution(s)
• Provide solutions for Hardware/ Software obsolescence management
• Be interface to and take complete ownership in managing the hardware/software deliverable from internal and external supplier
• Improving customer satisfaction through providing excellent solutions to existing customers
• Participate and perform risk analysis according to applicable medical device standards
• Deep understanding of US and international regulatory requirements and standards for a heavily regulated product (ISO 14971, IEC60601-1, IEC62336 EMC standard, etc.) preferred

You're the right fit if:

• Master/bachelor’s in engineering – Computer Science/Information Technology/Electronics/ Controls Engineering
• 10+ of experience in designing & developing medical devices / products with Minimum 5 years of experience in end-to-end design and development for subsystems (Control systems preferred)
• Experienced in design / development of complex technological products / systems / subsystems in functional area.
• Experienced in control system/Imaging software design and development preferred
• Experience is CT / Nuclear Medicine product development is preferred
• Experience in hardware/ software obsolescence management is preferred
• Knowledge of IEC standards, risk management, verification and validation of medical devices
• Knowhow of design control processes for medical device design
• Fast learner and interest to learn new technologies/business/systems
• System thinking mindset and domain expertise in the related area
• Excellent communication skills, Team player, Leadership skills and drive for results
• Mindset to simplify and reach to solutions with speed
• Knowledge of IEC 60601, IEC62304 standards, risk management, verification and validation of medical devices
• Develop a plan for the orderly phase-out of the software, ensuring users transition smoothly to new versions or alternatives.
• Prior experience with Installed base/LCM group preferred

This role 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 the lives of others.
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• Discover .
• Learn more about .