Electrical Designer - Pune, India - Philips
Description
Job Title:
Electrical Designer
Philips is a global leader in health technology, committed to improving billions of lives worldwide and striving to make the world healthier and more sustainable through innovation.
But it's not just what we do, it's who we are. We are 80,000, wonderfully unique individuals, with two things in common. An unwavering sense of purpose and a relentless determination to deliver on our customers' needs.
It's what inspires us to create meaningful solutions - the kind that make a real difference - when it matters most.
The world and our customers' needs are changing faster than ever before and while we are proud of what we do already, we know we can do more.
That's why we need you, to help us tackle increasingly complex challenges posed by ever evolving health and well-being needs.
In this role, you have the opportunity to make life better
Looking at the challenges the world is facing today Philips' purpose has never been more relevant.
So whatever your role, if you share our passion for helping others, you'll be working towards creating a better and fairer future for all.
In this role, you have the opportunity to
- Enrich global experience within medical domain and build expertise in medical device electronics engineering
- Invasive and Non-Invasive Class II/III medical device electronics hardware Design History Files (DHFs) remediation
- Design, develop and maintain electronics engineering aspects for sleep and respiratory care products like Hospital/Home Ventilators
- Identifying appropriate technologies solutions for overall system, subsystem and component levels
- Ensure solutions are consistent with the higherlevel architecture and requirements and complies with global regulatory and safety requirements.
- Manage EOL/Obsolescence issue in proactive manner
You are responsible for
- Design History File (DHF) remediation for electronics engineering deliverables which includes
- DHFs responsibilities for embedded systems, controllers & processors, digital and analog circuitry, power supplies, connectivity interfaces
- Develop and document designs in compliance with Quality Management System requirements
- Authoring and reviewing design documentation including requirements specification, design docs, engineering analysis, schematic capture, test plans, test procedures, test records
- Design and development of new circuitry to replace aging/obsolete parts
- Develop new platforms, Integrate new technology, simplify designs, improve reliability to improve performance of sophisticated respiratory care medical equipment
- Create robust, reliable electrical board/system designs for critical care medical (respiratory care) equipment with complex electromechanical, electropneumatic, user interface, patientresponse control, fault tolerance and regulatory requirements
- Support the assurance of supply of our products by resolving component obsolescence issues
- Drive the quality and performance of products by identifying opportunities for improvement from field, supplier and manufacturing data
- Support the manufacturing engineering team in troubleshooting and resolving issues discovered during production
- Work with Design for Excellence (DfX) mindset to plan and execute Design for Manufacturability (DFM), Design for Testability (DfT) and Design for Serviceability (DfS)
To succeed in this role, you should have the following skills and experience
- M.Tech /B.E/B.Tech Electronics Engineering from reputed institute
- 7+ years of relevant experience in electromechanical devices electronics hardware design, development and maintain. Nice to have medical devices electronics engineering experience
- End to end electronics hardware design & development, implementation, testing and documentation for electromechanical products
- Handson experience with embedded systems, controllers & processors, digital and analog circuitry, power supplies, connectivity interfaces
- Expertise in design documentation including requirements specification, design docs, engineering analysis, schematic capture, test plans, test procedures, test records
- Well versed with New Product Introduction (stage gate process) & Life Cycle Sustenance of medical product
- Exposure to Risk assessment tools & DFMEAs
- Handson experience in medical device documentation: DHF, DMR, BOM and Spec release
- Exposure to Modeling tools PSPICE, HyperLynx
- Exposure to International Quality and Regulatory Standards e.g. IEC, FDA, CFR, MDD, UL, CE, CSA, BIS
- Experience in IEC , IEC , IEC and IEC Safety standards.
- Experience in IEC EN 61326, FCC 15 EMC Standards
- Fluent in verbal and written English, proactive, cando attitude, team player, decisive and entrepreneurial attitude
- Display perseverance & agility wit
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