דרושים Associate Ux Designer ב-Philips ב-India, Bengaluru

The Electrical Designer will also be responsible for Electronics/ Electrical component obsolescence management, Reactive and Proactive obsolescence management, Redesign for cost reduction and improved reliability, Redesign for obsolescence mitigation, Failure, and root cause analysis, Alternate component sourcing, limited software release support, and regulatory updates are common sustaining activities.

Your role:

• Drive product development activities including development of design concepts, prototype testing, engineering specs, and module/system level tests.
• Drive continuous improvement projects related to design implementation, manufacturing process, product quality and reliability
• Work with Systems Engineering, Electrical and other cross functional team members to design electronic enclosures to meet system level functional and architectural requirements.
• Assess & create a Product Change Notification document for each change request/product defect.
• Root cause investigation of electrical issues that involves analysis of Schematics, board layout, assembly drawing and Bill of Materials.
• Assist in evaluating alternate components that are going in EOL, and lead design and qualification of alternate components at the system level.
• Create Module Requirements/Char Specification document for electrical modules
• Develop Test protocols which includes Module Verification plan & report
• Execute module verification testing and log results
• Perform release activities includes Design Verification Review, Design History File (DHF) update and write Memo’s as needed

You're the right fit if you have:

• Masters/ Bachelors in Electrical / Electronics Engineering from an accredited university
• 10 years minimum of experience in product design and development.

Skills

• Extensive experience in Analog and Digital circuit design experience preferably from Medtech industry
• Hands - on experience in component obsolescence management primarily in medical devices, consumer electronics, Automotive OEMs
• Expertise in design and deployment of test fixtures for module and system verification
• Experience with medical device standards (IEC 60601, ISO 13485, FDA 21 CFR Part 820)
• Cross-functional collaboration
• Root cause analysis and failure investigation by using Methodical, effective troubleshooting/problem solving skills.

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 the lives of others.
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to make life better

In this role you will bring innovative clinical solutions in 2D and 3D imaging and to our customers around the world. We help physicians to decide, guide, treat and confirm the right care in real time during a minimal invasive procedure to enable better outcomes for each patient. We touch patients’ lives when it matters most and we aim to do it in the most reliable, effective and sustainable way.

You are responsible for

Leading a full product(s) release cycle to ensure quality and compliance

Translation of user and business requirements into product requirements

Managing complexity of products in a multi-disciplinary and international set-up

Lead technically the requirements, design & product specifications for the system / subsystem

Monitoring and managing that the requirements and design is implemented correctly by the Agile Release Train

Drive design for Quality, Reliability and Serviceability of the system / subsystem

Performing safety analysis according to applicable medical device standards

Complying to all applicable medical standards / regulations such as CE (EU-MDR) and FDA

Support regulatory submissions activities

Support project manager on realization, planning and budgets

Contributes to future studies, technical concepts and program roadmap

Support post market surveillance activities

To succeed in this role, you’ll need a customer-first attitude and the following

Master's degree or equivalent in Engineering

Overall 15+ years of experience in the industry,several years of experience in designing & developing medical devices / products

Knowledge of IEC standards, risk management, verification and validation of software medical devices

Knowhow of design control processes for medical device design.

System thinking mindset and domain expertise in the related area.

Excellent communication skills

Leadership skills and drive for results

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and answers to some

Indicate if this role is an office/field/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 the lives of others.
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• Discover .
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You are responsible for

• Supporting product verification through the phases of the Medical Device lifecycle.

• Providing technical support and leadership on a cross-functional team

• Define, document, and continuously improve verification tests including conducting peer reviews and maintaining traceability to requirements

• Perform verification tests and conduct analysis of the test results to ensure complete verification of the requirements

• Identifying, analyzing and driving technical issues to resolution

• Perform work with little to no supervision as department subject-matter expert

• Participates in design reviews, including reviews of design verification plans, reports, and test artifacts.

• Development and execution of validation test plans , test records and Test fixtures

• Keeps abreast of new developments in all relevant technological domains.

• Provides technical leadership to ensure overall product development success.

• Keeps abreast of new developments in all relevant technological domains.

• Contributes to technology roadmaps and other strategic related activities

• Provides technical leadership to ensure overall product development success.

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

• Bachelor’s degree in Electronics/Computer Science/Electrical Engineering or related field, good to have a Master’s degree.

• Total 5+ years’ experience with Minimum 3 years of experience in medical device or other similar industry

• Demonstrated knowledge of global quality and regulatory environment for medical devices including FDA CFR 21 part 820.30 and IEC 60601-1-1 (CE mark), ISO 13485, and risk management requirements and development dependencies.

• Solid understanding of medical device product development, preferably Design Control experience with Class-III/Class-3 medical devices (FDA CFR Title 21, 820.30)

• Experience specific to product verification.

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

• Experience in designing and assessing compliance to national/international standards.

• Strong technical writing/documentation skills for a regulated medical device design environment, including requirements definition

• Proven ability to communicate in both verbal and written form to technical and non-technical customers, stakeholders, and various levels of management.

• Possess strategic agility/vision: Sees ahead clearly; can anticipate future concerns.

• Develops and maintains effective relationships and is capable of quickly earning trust and respect.

• Ability to study and understanding of Schematics and PCBA

• Board bring up experience.

• Good Knowledge of EMI/EMC (IEC- 60601-1-2)artifacts and testing , ISO 14971 (Risk Management), IEC 62304 (Software Lifecycle).

• Strong knowledge of embedded systems, real-time operating systems (RTOS), and microcontroller-based architectures.

• Proficient in test development tools, scripting languages (Python, Shell, etc.), and test automation frameworks.

• Experience with communication protocols (I2C, SPI, UART, CAN, BLE, etc.).

• Experience with hardware-in-the-loop (HIL) and system simulation environments.

• Experience with version control systems (Git) and requirements management tools.

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Job title: Senior Usability Designer

Usability designers and engineers ensure that products are intuitive: developing high-quality propositions that are safe, effective, efficient and satisfactory in use.

You are responsible for

• Work with other senior experts in the central Usability Excellence team to define enterprise level strategy, including KPI’s and measurement plans.

• Provide ad-hoc senior support for businesses regarding processes and regulations (FDA, IEC 62366.1, EU-MDR, NMPA)

• Be the first point of contact and escalation path for use related safety and quality concerns in Bangalore, safeguarding psychological safety.

• Work directly with business leads in Bangalore to raise awareness, develop capabilities, and align on processes, RACI’s, and timely involvement of usability specialists.

• Decide on changing scope or identify challenges and drive and initiate strategic roadmaps.

• Stay on top of developments and insights regarding medical device regulations for all markets, and pro-actively advise teams and leadership on developing needs.

• Help set the internal quality bar, define mechanisms and drive tactics to assess and hold underperforming teams accountable

• Contribute to enterprise level narrative, and leverage opportunities to engage, and evangelize internally

• Mentor more junior team members

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

• Bachelor's/Master's degree in a relevant field

• Minimum 12 -14 years of work experience with at least 7 years progressive experience as usability specialist or related, with at least 3 years of experience managing stakeholders in complex environments

• A usability rockstar who is highly specialized in one area of usability and/or very broadly experienced. Acknowledged expert (internally and externally) in their specific area of expertise.

• Academic background in industrial design, product design or cognitive science/psychology with focus on Human-Computer Interaction or human factors;

• Relevant medical domain knowledge, also on relevant side domains.

• Expert knowledge of usability methodologies, processes and standards, particularly regulatory standards (FDA, IEC 62366.1, EU-MDR);

• Understanding of (academic) design of experiments and statistical analysis;

• Experience in the end to end process of creation of products from requirements analysis to validation;

• Great communication, collaboration and leadership skills to perform with multidisciplinary and international (management-) teams.

Beneficial skills:

• Understanding of Quality System Regulations (QSR);

• Understanding of Risk Management process;

• Understanding of Agile product development;

• A getting-things-done mentality;

• Pro-active mindset.

• 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.Indicate if this role is an office/field/onsite role.About Philips
  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 commitment to diversity and inclusion .

You are responsible for:

• Driving project scope and outcomes as the main point of contact for product managers, developers, and other stakeholders, ensuring alignment and effective communication.

• Managing the entire design process, including concept ideation, wireframing, prototyping, final UI design, design specifications, implementation support, and design Quality Assurance (QA).

• Applying user-centered design principles and best practices to create consistent, high-quality user experiences aligned with the Philips brand and Design Language System (DLS).

• Supporting usability testing and leveraging insights to continuously refine and improve designs.

• Supporting UX telemetry efforts, identifying key metrics, event taxonomies, and tracking performance to measure design impact.

• Creating and maintaining standard design documentation in alignment with internal Quality Management Systems (QMS).

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

• Bachelor's or Master’s degree in Design, Interaction Design, Human-Computer Interaction, or a related field.

• Minimum 6-10 years of experience in UX design, preferably in the health tech industry.

• Proficiency in design tools like Figma, Sketch, and InVision, with the ability to adapt to emerging tools and trends.

• Familiarity with agile methodologies and tools.

• Strong analytical and problem-solving abilities for tackling complex design challenges.

• Ability to navigate ambiguity and propose innovative, user-centered solutions.

• Excellent communication skills, including proficiency in written and spoken English, to effectively collaborate with diverse teams, present ideas to stakeholders, and document processes. Proactive mindset for advocating user needs and driving design decisions that align with Philips' mission to deliver better care to more people

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 .

Our hybrid working model is defined in 3 ways:

Your role:

You will have the opportunity to shape how our software and digital services will improve the care and wellbeing of millions of people across the globe.

You apply a systems thinking approach to design and deliver superior experiences and interactions that work at the micro and macro levels. Your experience of working in cross-functional teams, in combination with your knowledge of industry standards and heuristics, allows you to efficiently deliver qualitative and scalable solutions from software applications to digitaldevices.​​​​​​​​​​​​​

• A nalysis/research: You are focused on understanding people, business and societies, framing the problem with a strong focus on user needs and requirements.
• Creation/validation: You are creating user focused strategies, innovations, solutions and experiences and the user testing and validation of these, considering usability, sustainability and appropriate visual and verbal articulation in line with DLS and Brand guidelines.
• Process/delivery: You are executing on scope, driving own efficiency, delivering appropriate design quality within budget and project parameters.
• Stakeholder focus: You are focusing on the customer, collaborating, partnering and co-creating with internal and external stakeholders, with clear and impactful communication and articulation of design decision making.
• Team: You are contributing to effective teamwork, receiving guidance and being a pro-active team player, offering a point of view.

You're the right fit if:

• You have a Bachelor’s degree in Design, Design Research or related discipline or equivalent professional Design training experience.
• You have min. 8 years of professional experience, preferably in the healthcare domain.
• You understand the context of design challenge and are empathetic to user and stakeholder needs and requirements.
• You generate proposals or solutions that meet the requirements, with appropriate visual and verbal articulation, applying relevant guidelines.
• You work with speed and within budget and time constraints set by the project and safeguard design quality.
• You work together with business stakeholders, using clear and concise communication.
• You contribute effectively as part of a team, receiving guidance from project or organizational lead.
• You have professional training and knowledge in UX/UI competence area, you can apply that in the context of a given assignment and continuously learns about latest trends and skills.
• You have good teamwork skills, and you clearly communicate and defend a point of view.
• You apply analysis skills to understand the problem, define an approach and apply diverging problem-solving skills.
• You apply innovative thinking from a User Experience perspective, you are pro-active, inquisitive and thinks out of the box.
• You have strong visualization, interaction, and prototyping skills (eg. Figma).
• You have good communication and presentation skills.
• You have the ability to collaborate with multidisciplinary professionals and stakeholders, from around the globe.
• You are excellent in verbal and written English.

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 .

to make life better

In this role you will bring innovative clinical solutions in 2D and 3D imaging and to our customers around the world. We help physicians to decide, guide, treat and confirm the right care in real time during a minimal invasive procedure to enable better outcomes for each patient. We touch patients’ lives when it matters most and we aim to do it in the most reliable, effective and sustainable way.

You are responsible for

Leading a full product(s) release cycle to ensure quality and compliance

Translation of user and business requirements into product requirements

Managing complexity of products in a multi-disciplinary and international set-up

Lead technically the requirements, design & product specifications for the system / subsystem

Monitoring and managing that the requirements and design is implemented correctly by the Agile Release Train

Drive design for Quality, Reliability and Serviceability of the system / subsystem

Performing safety analysis according to applicable medical device standards

Complying to all applicable medical standards / regulations such as CE (EU-MDR) and FDA

Support regulatory submissions activities

Support project manager on realization, planning and budgets

Contributes to future studies, technical concepts and program roadmap

Support post market surveillance activities

To succeed in this role, you’ll need a customer-first attitude and the following

Master's degree or equivalent in Engineering

Overall 15+ years of experience in the industry,several years of experience in designing & developing medical devices / products

Knowledge of IEC standards, risk management, verification and validation of software medical devices

Knowhow of design control processes for medical device design.

System thinking mindset and domain expertise in the related area.

Excellent communication skills

Leadership skills and drive for results

Visit our careers website to explore what it’s like, read stories from our, find information
and answers to some

Indicate if this role is an office/field/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 the lives of others.
• Learn more about .
• Discover .
• Learn more about .