דרושים System Designer - Image Chain ב-Philips ב-India, Pune

Your role:

• In this role, you have the opportunity toKey Requirement:
  ▪▪
  End to End engineering support for supplier-initiated change requests includes part design, tooling, and manufacturing location changes·
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  Follow design controls governed by FDA· Should have hands on experience of Design verification, Validation, protocol documentation.
  ▪▪
  Conduct DFM, DFA reviews with suppliers.
  ▪
  Should have hands on experience on Windchill

You're the right fit if you have:

• To succeed in this role, you should have the following skills and experience
• •B.S. in Mechanical Engineering with 8-12 years of proven design engineering and product development experience
  Experience supporting supplier transfer & sustaining projects
• •Demonstrated strong analytical and problem-solving skills
  •Knowledge of manufacturing quality systems and working in a regulated industry
  •Experience with geometric dimensioning and tolerance
  •Strong English written and verbal communication skills required
  •Creates 3D models, assembly and detailing including drawing conversions
  •Apply GD&T and perform Tolerance stack-up analysis for components/Sub-system.
  •Review and ensure adequacy of supplier part qualification activities
  •Performing hand calculations for design feasibility
  •Shall have hands-on expertise in Engineering change Management
  •Provide technical support to suppliers & other departments to fulfil project/productions

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 .

• 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.
• 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 .

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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Mechanical Engineer

Job Description-

You are responsible for executing engineering requirements analysis, developing, and validating test plans, and ensuring compliance with regulatory standards, working under general supervision. The role documents design specifications and results, implementing design improvements, and troubleshooting technical issues, while mentoring junior team members. The role participates in design reviews, provides insights for continuous improvement, and adheres to company policies and quality standards. The role evaluates external vendors and technologies for integration, maintains component performance and reliability, and fosters strategic partnerships to enhance product innovation

Your role:

• Design and detail components and systems
• Obtain parts and create prototypes.
• Successfully interact with associates in other departments, such as Manufacturing Operations, Procurement, and engineering staff, to achieve project and product objectives.
• Be a highly motivated, self-disciplined, open-minded individual possessing hands-on skills.

• Requirements detailing, design specification preparation, implementation, test, and integration of Unit per the higher-level Requirement and - Design specifications/architectures.
• Ensures the mutual consistency and efficient integration of the separate modules in modular, easy-to-maintain units that meet the product specification.
• Understands and communicates the consequences of their design on the architecture.
• Determines the Unit interfaces (HW/SW) in close consultation with relevant disciplines.
• Ensures that there is proper documentation for his/her design.
• Keeps abreast of technical developments in own field through study of the literature and technical contacts and propagates it.
• Define, execute, and take the lead in concept and feasibility studies with a limited scope to investigate the usability of new technologies.
• Contributes to technology roadmaps and other strategic-related activities.
• Takes technological or process-related improvements initiatives within the scope of at least the mechanical development group.
• Contributes to the Work Breakdown Structure/ the planning process of his/her area.
• Draws up personal schedule and reports on progress.
• Inspires team members to get the job done.
• Performs work in line with the processes that have been agreed in the department.

You're the right fit if:

• Bachelor's Degree/ Vocational Education in Engineering, (8 to 10 years exp)
• 8-10 years of relevant experience in design & development of electro-mechanical sub-systems & systems.
• Strong communication and collaborative abilities proactively seek out expertise and advice and input from others in a collaborative team-environment, Project Management skills (Dealing with suppliers)
• In-depth knowledge and 8+ years of experience in the development of mechanical design
• Experience in creating design concepts and mechanical designs of complex parts or assemblies.
• Strong knowledge and experience in CAD/CAE. such Creo, NX,, LCM- Life cycle management.
• Experience in metal or plastic crafts would be appreciated
• Experience in PDM/ PLM (Windchill)
• Good knowledge of Development methodology
• Six Sigma green belt is a plus

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 sustain and maintain labeling system software, hardware and processes in a medical device manufacturing environment.

Your role:

• Develop and maintain a complete labeling system (software, processes and equipment) for complex medical devices.

• You are responsible for: the development sustaining of a complete labeling system solution software; the quality and compliance of medical device labeling; internal and external database management; validation activities (software and hardware); and departmental work instructions/processes.

• Deployment and administration of a complete labeling system, including documented Work Instructions (WIs) and departmental Standard Operating Procedures (SOPs).

• Ensuring timely change management of labeling and Instructions For Use (IFUs), working with labeling technicians/label coordinators, and performing labeling changes.

• Quality management and all life-cycle phases of product labeling and IFUs. Leadership, both direct and indirect, will be an expectation of this role as a growth path.

You're the right fit if:

• You’ve acquired 1+ year of engineering experience in medical device or other highly regulated industry.
  Your skills include supporting quality related investigations and changes involving labeling materials and/or labeling processes, such as NCRs, CAPA, SICRs, IIAs, Audit Support questions, Equipment Events, Regulatory Gap Assessments, etc.

• You have a B.S. in Engineering.

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

• You’re an excellent communicator that is detail oriented and well organized.

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.

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The pay range for this position in CO is $71,250 to $114,000

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 Plymouth, MN .

Your role:

• Lead and execute multi-disciplinary programs, ensuring alignment with scope, timelines, and budgets.
• Drive end-to-end Supply Chain transformation initiatives , from strategy to execution.
• Apply entrepreneurial thinking and structured problem-solving to drive innovation and efficiency.
• Leverage your knowledge of supply chain, market dynamics, and business functions to influence decision-making.
• Identify gaps, assess business priorities, and tap into internal networks to deliver results.

You're the right fit if you have:

12–15 years in industrial environments with strong expertise in Supply Chain Management (Supply Chain Management)
Supply Chain Management (SCM), Inventory Management, Project & Program Management.
Bachelor’s in engineering (Mechanical, Electrical, or Electronics) , PMP Certification preferred
Strong communication skills, a positive attitude, and a proactive approach , excellent stakeholder management

Why Join Us?

• Work on impactful programs that shape the future of our supply chain.
• Collaborate with passionate professionals in a dynamic, growth-oriented environment.
• Be part of a company that values innovation, integrity, and continuous improvement.

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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