דרושים Sr Product Quality Engineer ב-Philips ב-India, Pune

Work on achieving a state of high quality performance at our Supplier partners. You will pursue continuous quality improvement through the application of Quality Engineering practices on Philipsproducts/parts/services

You are responsible for

• Reviewing Supplier Quality Agreements
• Analyze defects to determine if they are supplier caused and notify accordingly
• Managing/Issuing/Following up on Supplier Corrective Action Requests
• APQP execution, monitoring and control as part of Sustaining Changes (Life Cycle Engineering)
• Supplier performance monitoring, reporting, improvement and development
• Support Supplier quality risk assessment and mitigation
• Acceptance of products that have gone through NPI process before official release
• Support Supplier audit schedule development and maintenance for audits related to supplier processes, supplier selection,corrective/preventiveaction verification
• Assess and coordinate Supplier Change Requests
• DEFOA analysis and securing reoccurrence

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

• Bachelor’s degree in Electrical/Electronic/Mechanical Engineering (Prefer E&E) or other scientific field, or equivalent experience
• Minimum 10+ years’ experience in supplier quality in a highly regulated industry (PCB/Coils experience is a must, having IPC standard knowledge is added advantage)
• Detailed knowledge and experience of APQP and related PPAP tools
• Well versed in Quality Engineering and Continuous Improvement techniques
• Participated in several NPIs from start to finish
• Direct shop-floor production engineering sustaining experience
• Strong negotiation skills and ability to lead through influence
• Experience having direct working relationships with suppliers
• Flexible mindset and proactive approach
• Excellent communication skills in English
• Willingness to travel up to 20% of the time

In return, we offer you

We welcome you to a challenging, innovative environment with great opportunities for you to explore.

Our benefits are very competitive and designed around your preferences:

• A market conform salary
• 25 Days of leave and the possibility to purchase up to 20 extra days off annually
• A variable bonus based on both Philips results and personal performance
• Extensive set of tools to drive your career, such as a personal development budget, free training and coaching
• Solid company pension scheme and attractive collective health insurance package
• Opportunity to buy Philips shares and products with discount
• Healthy work-life balance

Job title:
Data Analyst- Design Quality Engineer

Your role:

• In partnership with other functions, execute on defines defining and manages managing the holistic patient/ and consumer user safety, quality and reliability strategy and approach, overseeing execution with focus on data quality and quality of results, driving to sufficient confidence in the product/service prior to and post release to market.​
• On request of the organization, provide the relevant data analytics and effectively analyze and utilize post-market data on the product’s field performance to identify system performance trends and/or improvement opportunities to continuously enhance Patient Safety and product quality and reliability.
• Be a contributing member of the data analytics organization and community.
• Identify opportunities for standardization of data analytics requests, based on frequency of business requests and their impact and priority.
• Align on the standardization of data analytics and drive automation with the team(s) that perform complex data analytics computations and develop advanced, effective and robust data solutions to support the business.
• Execute testing to support the validation of data and data analytics solutions.
• Validating key design inputs like e.g useability, reliability, performance, safety, quality and their related test strategies to ensure appropriate statistical confidence and reliability levels.​​
• Leading quality related problem solving.
• Developingand maintainingthe knowledge and expertise resulting in state-of-the-art approaches to structured, data-driven product development, manufacturing and maintenance strategies that increase confidence and reliability of the safety and quality characteristics of our products. You will help to deploy best practices throughout the business by providing training, coaching and support to relevant functions.

You're the right fit if: (4 x bullets max)
1. Experience.- 8+ of industry experience in field of data analyst for Quality function, understand ISO 13485, preparing Dashboard and analysis.
2. Skills.- SQL, Python, Statistical Methodology, ML Experience
3. Education.- Any engineering
4. Anything else.- Good Communication and presentation skill, experience in SAP/Aries will be added advantage. This is an individual contributor role.
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.
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Job Responsibilities:

• Facilitates technical capability assessments of potential new suppliers, ensuring they meet the company's quality standards, and contributes to the supplier selection.

• Conducts & reviews DFMAT (Design for Manufacturing and Assembly Technique), SRPQP, PFMEA (Process Failure Mode and Effects Analysis), Control Plan, SPC (Statistical Process Control), PV&V (Process Validation(IQ/OQ/PQ/TMV) and Verification), FAI (First Article Inspection), LRA (Line Readiness Assessment), and SICR (Supplier Initiated Change Request).

• Develops, executes, monitors, and controls APQP (Advanced Product Quality Planning) plans as part of the NPI process to ensure consistent product quality.

• Contributes to the content of the Supplier Project Book, documenting detailed quality requirements and expectations for suppliers.

• Facilitates collaboration between R&D and suppliers in Design for Excellence (DfX) initiatives to enhance product design quality and innovation.

• Focuses that Critical to Quality (CtQ) characteristics are effectively communicated to suppliers and rigorously maintained throughout the production process.

• Coordinates Part Submission Warrant plans, deliverables, line releases, and completion, ensuring all parts meet specified quality standards before approval.

• Executes supplier improvement and development initiatives on APQP(Advanced Product Quality Planning), providing guidance and resources to enhance supplier processes, ensuring they meet the high standards required for production quality and efficiency.

• Assists with the process of making additions, changes, or deletions to the Approved Supplier List, ensuring that only qualified suppliers are retained.

• Supports in end to end performance management of suppliers, conducts detailed analysis of defects to determine if they are supplier-caused, and acts as an independent reviewer for Supplier Corrective Action Requests.

Bachelor's/Master's Degree in Engineering Science, Mechanical, Electrical Engineering, Electronic Engineering or equivalent.
Minimum 12-15 years of experience with Bachelor's in areas such as Quality Engineering, Safety Engineering, Process Engineering, Process Validation, Continuous Improvement TechniquesB.E Electronics/Mechanical/Electrical

LEAN Six Sigma or equivalent.
• Supplier Quality Management
• Quality Management Procedures and Methodologies
• Supplier Evaluation Methodologies
• Data Analysis & Interpretation
• DfX Methodology
• Supply Chain Management (SCM)
• ISO13485:2016, FDA 21CFR 820
• CAPA Methodologies
• Statistical Process Control (SPC)
• Measurement Systems Analysis (MSA)
• Process Validation(IQ/OQ/PQ/TMV)
• First Article Inspections
• Documentation & Reporting
• Regulatory Requirements
• Continuous Improvement

Our hybrid working model is defined in 3 ways:

Quality Manager - MR Coils/OEM

Your role:

• Establishes operational objectives and work plans, delegates assignments to subordinates to ensure smooth execution and efficient distribution of tasks within the organization and fosters collaboration and productivity while aligning with overarching goals.
• Reviews and monitors operational key performance indicators (KPIs) to evaluate the success of operations, actively participates in the development, modification, and execution of company policies impacting immediate operations, with potential implications across the organization.
• Utilizes wide-ranging experience and professional expertise, creatively resolves complex issues aligned with company objectives, distinguished by additional specialized knowledge and recognized as an expert in the field.
• Guides the review and approval of finished products manufactured for and by the company, manages all inspections and inquiries regarding the operation of manufacturing sites and collaborates with relevant company groups to ensure compliance with company standards, regulations and approved manufacturing process specifications.
• Manages talent across the quality assurance team, while driving employee selection, performance management, compensation management, career development, and ensuring effective operational management.
•Oversees material and spare part qualification, coordinates enhancements in supplier processes for critical-to-quality parameters, ensures implementation of supplier process control plans with control limits and tolerances
• Implements quality assurance policies and strategies to determine methods, techniques, and evaluation criteria in quality assurance, ensuring alignment with organizational objectives for optimal outcomes.
•
• Owns supplier qualification, audits, and assessments processes, supports in external and internal audits, aids in regulatory compliance gap closure, monitors supplier quality metrics, agreements, and records, and participates in supplier quality-related communication and feedback.
• Manages talent across the team, while driving employee selection, performance management, compensation management, career development, and ensuring effective operational management.(4 x bullets max)
1. Experience- 8+years of Medical device (Medtech) industry experience
2. Skills- End- End Quality Management experience, CAPA Management, Quality Assurance, Risk Management, Quality Control, Regulatory Compliance
3. Education- Bachelor's degree in Any engineering
4. Anything else- People Management Experience, Business Acumen, Good communication Skill, Coordinating/hosting audits and inspections,problem Solver, Result oriented

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.
• Learn more about .
• Discover .
• Learn more about .

Your role:

• Drives supplier participation in BoM RFPs for technical fit and cost competitiveness

• Leads DfX initiatives to optimize cost, quality, and product performance

• Facilitates early supplier innovation and integrates it into design

• Partners with Engineering to leverage supplier expertise and influence specifications

• Champions product cost and quality strategies across the portfolio

• Ensures supplier readiness for New Product Introductions

• Builds cost roadmaps post-launch, driving continuous improvements

• Shapes cost engineering strategies through cross-functional collaboration

• Executes impactful sourcing, cost, and risk reduction projects

You're the right fit if you have:

• Bachelor's/ Master's Degree in Electrical, Electronics, Mechanical Engineering.

• 10+ years of proven expertise in Product Sourcing, Supplier Innovation, and Cost Engineering, consistently driving value through strategic supplier engagement, technical insights, and process optimization.

Key Skills:

• DfX (Design for Excellence) – cost, quality & risk optimization

• BoM RFP Leadership – supplier engagement & pricing strategy

• Cost Roadmapping – lifecycle cost planning & control

• Supplier Innovation – early collaboration & integration

• New Product Introduction (NPI) – supplier readiness & ramp-up

• Manufacturing Know-how – process capability & industrialization

• Cost Engineering – analysis & reduction strategies

• Cross-Functional Collaboration – engineering, innovation & sourcing teams

• Project Management – strategic sourcing initiatives

• Supplier Relationship Management – partnerships & performance

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 .

Sr Norm Compliance Officer

As a multi-business modality hub, HIC innovates across product lines, including Image-Guided Therapy (IGT), Precision Diagnosis, and Connected Care. Teams of R&D, design, software developers, mechatronics & product marketing work together to build a product starting from market requirement understanding until delivery. Products innovated and manufactured at HIC are launched/ shipped in both Indian and global markets.

Your role:

In this role, you have the opportunity tosupport the Norm Compliance activity for IGT-MoS products with all relevant mandatory international and national regulations including MDD & MDR and Philips Healthcare processes.

• Own norm compliance portfolio for IGT MoS products and execute end to end activities in accordance with regulations.
• Work on the project deliverables related to Norm Compliance release evidence –Generate Technical File for MDD & MRDR certification.
• Identification of relevant clauses from standards for (sub)system,Standards mainly includes IEC60601-1, IEC60601-1-2, IEC60601-1-3 etc.
• Definition of product requirements to assure norm-compliance.
• Decomposition towards the individual (sub)system elements.
• Secure the implementation and verification of all specified legal requirements.
• Support with respect to technicalrealization/engineeringof norm compliance of the (sub) system.
• Support the verification (testing, witnessing and reporting and approval) of all specified legal requirements.
• Be the intermediary between development andcertifying/regulatoryagencies (UL/CSA/FDA/BSIetc).
• Test lab interaction experience.
• Support arrangements for and completion of submission to certifying agencies.
• Review standard updates and deploy revised standards.
• Identification of approbation consequences due to change requests. (Notified Body Audits)
• Train and inculcate design and cross functional teams on regulatory standards, update and execution.
• Contributing to Technology Roadmaps
• Build norm compliance team and coach them on various activities with the portfolio

You're the right fit if:

• B Tech / M.Tech/ME in bio-medical engineering having IQ specialization with ~12+ years of experience withminimum 5 years of experience in the X-ray system/subsystem design & development (or at least two end to end X-ray product development)
• In depth understanding of system wide IQ, combining IQ related theory (e.g. x-ray physics, image processing, visual perception, etc.) with understanding of relevant products and the application by the end-user.
• Knowledge of relevant regulations (UL, CSA, IEC, ISO, MDD, CE, etc.) and relevant standards (General Safety, EMC, Radiation Safety, Risk Management, Environmental, Sustainability, etc.).
• Knowledge on project organization, PCP and ISO 13485.
• Knowledge of IEC 60601 standards, risk management, verification and validation of medical devices
• Knowhow of design control processes for medical device design
• Working knowledge of cabling design, design for EMI/EMC, Design for reliability
• Good team player and ability to work independently & act pro-actively.
• Analytical, creative and abstract thinker.
• Ability to communicate (both written and verbal) on different levels.
• Is capable to introduce efficiency improvements on project level (change management).
• System thinking mindset and domain expertise in the related area
• Fast learner and interest to learn new technologies/business/systems
• Be structured and self-organized
• Excellent communication skills
• Team player, leadership skills and drive for results
• Mindset to simplify and reach to solutions with speed
• Intercultural sensitivity
• Self-motivation

How we work together

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.
• Learn more about .
• Discover .
• Learn more about .