דרושים Architect - Test Verification Engineering ב-Philips ב-India, Pune

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

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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.
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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 .

Senior Engineering Manager

Experienced Senior Engineering Manager to lead our R&D X-ray Image Chain (Detectors, Grids, Collimator, Tubes and Generators etc.) team and oversee our Norm Compliance Officers. This dual role requires a blend of technical acumen and people leadership to ensure the successful development and compliance of our diagnostic X-ray systems.

Engineering Management

• Lead and mentor the R&D Image Chain Components (flat panel X-ray detectors, anti-scatter grids, generators, collimators and tubes)

• Oversee pre-development, product introductions, and lifecycle management of Image Chain Components.

• Manage Image Chain components road mapping in collaboration with external suppliers & releases with an international, cross-functional team.

• Coordinate technical investigations into customer complaints.

• Supervise Image chain advanced development activities.

• Ensure product quality through thorough tests and requirements engineering.

• Collaborate on software development projects.

Norm Compliance Leadership

• Review product requirements related to safety, EMC, and environmental standards like IEC, EN, and ISO.

• Oversee compliance test plans, including standards such as IEC60601 series and ISO 10993.

• Oversee risk assessment and mitigation for product safety.

• Support usability and software teams in creating certification documentation.

• Ensure third-party component compliance and liaise with certification agencies (like TUV/CSA).

• Oversee technical file deliverables for MDD, MDR, RED, REACH, and RoHS regulations.

• Support audits and regulatory submissions (FDA, Notified Body, INMETRO).

• Maintain DXR compliance lab qualifications according to ISO17025.

• Train and guide cross-functional teams on regulatory standards and compliance execution.

• Stay updated on regulatory changes and timely closure of standards gap assessments.

Job Knowledge, Skills and Experience:

• Educational Background : BE, BTech, ME, or MTech degree, preferably in Biomedical, Electrical, Electronics, or Instrumentation.

Experience:

• Minimum 15 years in R&D and engineering roles, with 3 to 5 years in System Engineering (preferably in product safety and norm compliance)

• Minimum 3 years of people management experience

Technical Skills:

• Medical device design and development experience in imaging modalities (like X-Ray, CT, MRI, Ultrasound)

• System Engineering - preferred experience with Image Chain/Acquisition, product safety and compliance

• Proficiency in regulatory submissions and relevant compliance standards (e.g., CE Marking, FDA, Health Canada).

• Preferred experience in product design and managing compliance documentation.

• Preferred familiarity with IEC62304, ISO14971, IEC60601 series and ISO 10993

Leadership Skills:

• Proven leadership and mentoring abilities.

• Strong problem-solving and project management skills.

• Excellent communication and stakeholder management capabilities.

• Ability to train and develop team members on compliance and regulatory standards.

Personal Traits:

• Detail-oriented with high ethical standards.

• Adaptability to regulatory changes and proactive learning approach.

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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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Your role:

• Creates high quality working software to deliver with excellence towards customer’s expectations

• Features driven development in an agile approach

• Actively participates in sprint planning, daily stand-up meetings, sprint reviews, sprint retrospectives and backlog refinement

• Contributes to continuous improvement of the team, software and processes

• Designs, codes, documents, tests (automated), maintains and deploys software

• Supports DevOps in deploying software

• Sets, monitors and ensures to meet own performance metrics

• Defines, monitors and meets performance and quality metrics

• Provides technical solutions that conform to requirements with a strong focus on end-users, high quality (QMS/regulatory standards), performance, safety and security

• Keeps abreast of technical knowledge by studying and implementing state-of-the-art programming techniques and development tools, participating in educational opportunities, participating in communities of practice, reading professional publications and maintaining personal networks

• Software is developed to log / store performance data, usage, errors etc. and enable continuous monitoring of solution and product

• Develop software APIs / plug and play for integrating the latest AI models in a seamless fashion in products and solution

• Leverage data driven insights and AI enabled tools to improve code quality and performance

• Knows the customers well and uses that knowledge in the role

• Takes data driven decisions

• Participates in full process, working in pairing mode with equal

• Is the technical coach of a team or domain, recognized and approached by team members and shares knowledge across teams

• Understands clinical/application domain and systems

• Able to generate new solutions from vague problem statements. Full ownership for creating requirements

You're the right fit if:

• BE/BTech/MCA/MTech with 9-14 Years of exp in Embedded Systems

• As a Senior Engineer with expertise in Embedded Systems, you will play a crucial role in designing, developing, and maintaining Device software.

• This role is focused on hands-on work, but it also requires the ability to own things, direct others and architect solutions.

• Software design and development in embedded applications using C/C++ is required.

• Experience in Real-time operating systems (RTOS).

• Experience in software development in medical industry or highly regulated industry.

• Experience with IEC 62304, FDA guidance for medical device development and other relevant medical device regulatory standards is highly preferred

• Experience in Agile SW Development practices.

• Experience in scaled agile framework (SAFe) is preferred Demonstrated experience working with real time operating systems.

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 .
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