Create, develop projects and lead high impact projects backed by strong business cases in complex Image guided therapy systems
As part of Systems Engineering team: Drive continuous improvements across legacy and platform systems to support global product health & performance.
Apply AI, Six Sigma methodologies & continuously improve efficiencies, cost down for improved order intake & margin expansion with cross‑functional collaboration.
Perform DFMEA, risk management, Perform safety assessment of medical device in a cross-functional environment
Develop system level compatibility reports between Philips platform to third party medical devices that form a solution to the customers (patients & hospitals)
Interact with cross functional stake holders to assimilate relevant information to mature the scope of various sustenance problems, 3rd party compatibilities/ideas in the IGT-S business
Left-right look of & analysis of problem/idea under consideration to evaluate the inter-disciplinary engineering impacts and opportunities (interface design specifications, interface usage specifications, signal integrity, speed & power efficiency, system integration, functional system engineering, technology upgrade, EMC, reliability, manufacturability, usability)
Fine tune the requirements, design, verification and integration of module/sub-system in accordance with the higher-level architectural requirements and design specifications
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Ensuring that the design is consistent with the higher-level architecture and requirements
Responsible for ensuring that the design meets the performance, quality and cost criteria
Conduct concept and feasibility studies, address Corrective and Preventive Actions, complete the technical maturity analysis (including design specification availability, assessment of the extent of design efforts required) of the problems / ideas under consideration.
Define the test scopes
Ensuring the release of Design Verification & Validation plan & reports
Norm (Standards) and Regulatory Compliance Impact Analysis
Product Safety Risk impact analysis for the problem/idea under consideration
Report out the technical maturity, risk and mitigation strategies to the relevant stakeholders and facilitate the go/no-go decision about the problem/idea
Partner with project manager to define engineering scope and work breakdown structure
Ensuring that there is proper documentation per relevant standards & Quality Management System for the developed/assessed design
Ensuring the mutual consistency and efficient integration of the separate components in modular design that meets the product specification
Drawing up personal schedule and reports on progress
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
Problem/idea evaluation and efficient verbal/written communication
Handles the integration and optimization of a single component or straightforward subsystem within the system, ensuring seamless transfer and adherence to established quality and performance standards.
Global Collaboration
Work closely with Philips R&D centers across India (Pune, Bangalore) and global teams in the Netherlands and across the worldwide supply base, operations, Service and markets.
Integrate diverse industry technologies, trends (example AI, predictive condition monitoring of installed base) into Philips products, solutions delivered to hospital customers.
Minimum required Education:
Bachelors in engineering in Mechanical / Electrical / Mechatronics/ Bio-medical engineering and with a flair for systems engineering in MedTech devices.
Masters degree is a preference
You're the right fit if:
8 to 12 years of Analog & Digital engineering experience with solid system engineering understanding
Hands-on experience with tools like Track Wise, Clear-quest, Windchill, DOORs or equivalent will be an added advantage
Disciplined & result oriented team player
Ability to work independently under minimal supervision
Ability to present and articulate ideas to key stakeholders and leadership team
Excellent communication skills and a 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
New Product Introduction (NPI) and Product Life Cycle Management
Product Obsolescence Management/Sustenance and Value Engineering
Understanding & on the job application of standards like ISO 14971, ISO 13485, IEC 60601-1
Understanding & exposure to regulatory aspects pertaining to FDA, MDR, NMPA, TGA, HC, MHLW
Understanding & Exposure to D/P-FMEA, Design for Usability, Design for Manufacturing/Assembly, Design for Reliability
Understanding of Supplier Quality Management, Manufacturing Engineering, Operations and procurement will be added advantage
Strong experience in systems engineering within complex mechatronic, imaging, or MedTech systems.
Demonstrated ability to operate in multi-disciplinary technical teams and influence global stakeholders.
Experience in requirements engineering, requirements flow-down to component level, performing DFMEA, product concept development, Element requirements development,
Experience V&V, system integration, and risk management in hardware products
Proven background in sustaining engineering, supply chain improvement, or lifecycle management and driving cost down.
Preferred Experience:
Medical Device Industry Experience
Preferred Skills:
Systems Engineering
Hardware Engineering
Regulatory Compliance
Stakeholder Management
Project Management
Technology Acumen
System Testing
Testing Procedures & Tools
Process Improvements
Supplier Transfer Expertise
Supplier Quality Management
Primary Location
Pune
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 our business.
Discover our rich and exciting history.
Learn more about our purpose.
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 here.
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