דרושים Director - Mr R&d Components Hardware Engineering ב-Philips ב-India, Pune

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.
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• 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.
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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 .

As a Senior Hardware Engineer for high-volume consumer medical devices, you should be capable of architecting, designing, documenting, and implementing high-quality electronics on multiple platforms across multiple product ranges.

• This includes but is not limited to:

  • Hardware development using 8-bit micro-controllers up to 32-bit microcontrollers, battery charging circuits, and BLE radios.

  • Document, manage, and help to define/obtain/refine requirements, design docs, design reviews, and verification procedures,

  • Help establish consistent ways of working with respect to embedded system electronics/software/firmware.

  Requirements:

  • Degree in Electrical or Electronics Engineering.8+ years of experience in electronics hardware development in a professional organization, ideally in the Medical Device industry.

  • Hands-on knowledge of small micro-controllers and analog interfaces.

  • Mastery of oscilloscopes, function generators, power supplies, IDE’s and emulators for debugging and test.

  • Technical leadership skills in a multi-discipline engineering project environment.

  • Understanding of board and system-level technologies and the ability to read, interpret and review analog and digital circuit schematics.

  • Experience with electronics simulation tools such as PSpice.

  • Experience in wireless technologies such as BLE, Wi-Fi, Zigbee, etc.

  Desirable:

  • Experience in a regulated industry (FDA strongly preferred).

  • Six Sigma Black Belt certification.

  • Experience with Altium and Mentor Graphics tools for PCBA design.

  • Experience in defining, designing, documenting, testing, and implementing embedded firmware for 8-bit up to 32-bit microcontrollers using C.

  • Basic concepts of system architecture, systems engineering, and model-based design.

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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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As the Senior Director, Global Sustaining Engineering, you will lead a large, dynamic R&D team focused on sustaining and optimizing Philips' Medical and Personal Health product portfolio at our Pune site. You will drive innovation, enhance product lifecycle management, and ensure operational excellence across the supply chain, BOM productivity, and sourcing. This role demands a strategic leader with an entrepreneurial mindset, capable of transforming the organization and contributing to significant business growth. You will build and develop a global capability center, establishing Pune as a center of excellence.

Your role:

• Develop and implement R&D strategies aligned with Philips' global objectives, contributing to the 5-year Strategic Plan of Record.

• Establish and grow Centers of Excellence (CoE) for critical technologies (e.g., Plastics, PCBA, Sheet Metal, Systems Engineering, Power Distribution Unit).

• Define and execute the Pune site's strategic roadmap, driving organizational transformation.

• Manage and influence changes to operational processes and procedures across a global matrix organization.

• Shape the future of Philips’ product portfolio by leading R&D strategies that enhance product lifecycle management, supply chain efficiency, and cost optimization.

• Lead a high-performing team of 300-400+ engineers, collaborating with global business leaders, R&D teams, supplier quality, and regulatory stakeholders.

• Provide technical leadership and guidance, ensuring projects meet regulatory requirements and quality standards.

• Manage budgets, CAPEX, and resource allocation effectively, defining function-level budgets with multiple cost centers.

• Oversee Life Cycle Management (LCM) activities, factory SCR/ECR management, CoNQ management, and supply chain de-risking strategies.

• Establish and lead a dedicated factory-sustaining engineering team, performing a skill gap analysis and defining ways of working.

• Drive BOM productivity and assurance of supply, contributing to significant cost savings.

• Manage product performance, regulatory compliance, and product reliability.

Key Performance Indicators:

Including but not limited to:

• Technical growth/leadership

• Stakeholder management

• On-time delivery to commitments

• LCM Ownership (workstream ownership)

• Funnel BOM Productivity & Assurance of Supply

You're the right fit if, you:

• Have 20+ years of experience in engineering leadership, preferably in the medical or healthcare industry.

• Possess strong technical expertise in lifecycle management, supply chain strategies, and operational excellence.

• Hold a master’s degree in a relevant technical field or equivalent.

• Demonstrated a proven track record of leading large, cross-functional teams in a global matrix organization and driving business transformation.

• Have strong financial acumen and experience in managing budgets and resources.

• Deep understanding of PDLM/MLD processes and V-model product development.

• Have experience building and leading global capability centers.

• Have advanced knowledge of Radio Frequency Coils, Magnetic Resonance, Computed Tomography, and Digital X-ray systems or equivalent product development & R&D capabilities managed in various industries.

Onsite roles require a full-time presence in the company’s facilities.This role is onsite-based.• Learn more about
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