Systems Engineer

3 - 6 years

5 - 8 Lacs

Posted:9 hours ago| Platform: Naukri logo

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Job Description

Job Title Systems Engineer
Job Description
Emergency Care Business:
In late January, we announced that Bridgefield Capital signed an agreement to acquire Philips Emergency Care business which includes leading brands and products like HeartStart AEDs, Intrepid and DFM100 monitor defibrillators, Tempus monitor and Tempus ALS systems, and Corsium and ECI informatics solutions. We expect the transaction to close at the end of 2025.
With Bridgefield s support and building on our 40+ year legacy of growth and innovation in emergency medical technology, the Emergency Care business will continue passionately pursuing our mission of saving lives, lowering the cost of healthcare, and advancing the science of resuscitation while serving the public access AED, EMS, military, and hospital market segments.
Systems Engineer
In this role, you have the opportunity to
Be an integral part of the Emergency Care and Resuscitation (ECR) R&D team, actively participating in cardiac defibrillator product development. ECR team has a broad product portfolio of advanced life support solutions, automated external defibrillators, monitoring and data management solutions. Our mission is to design, produce, and deliver every solution as if the life of someone we love depends on it. Every day, we empower and enable our customers from clinicians to paramedics, first responders to the everyman to save lives using our innovative, market-leading technology.
We are looking for a passionate Systems Engineer to join us as we strengthen our product portfolio, expand our services and solutions, and bring game-changing technology to the market. This team member will be responsible for working collaboratively with a team of cross-functional engineers.
Your role:
  • Translation of user and business requirements into product requirements, high-level product design, check, and optimize integration and verification.
  • System decomposition and allocation of derived requirements down to HW/SW element and part level, and related traceability.
  • Trade-off of product/system design specifications and interfaces, determine the feasibility of potential solutions, and lead technical & design reviews.
  • Ensuring full Product Safety Risk Management in a regulation-compliant manner.
  • Managing technological complexity of products in multi-disciplinary settings. Develops products, independently and according to ones own judgement, using the latest technologies and resources, often realizing systems based on unverified specifications.
  • Makes a substantial contribution to the innovation of products and processes.
  • Makes independent choices regarding aspects of the design. Gives reasons for changes in specifications.
  • Formulates assignments in dialogue with the customer or user.
  • Submits ideas for future developments and provides tangible input for Technology roadmaps.
  • Develops partly and sometimes wholly new products, processes, or technologies.
  • Elicits, reviews, and characterizes stakeholder feedback; creates and reviews system-user interaction model with various Systems Engineering related Methods/tools
Youre the right fit if:
  • Bachelors in a relevant field, including Electrical, Electronics, or other related science.
  • A minimum of 5 years of experience successfully developing complex medical devices (hardware, software, consumables) Products for acute/emergency care/hospital markets are necessary.
  • Have Systems Engineering certification
  • Hands-on experience in ISO 13485, ISO 14971, ISO 20417, IEC 60601-1, and collateral
  • Hands-on experience in requirements management, including developing, deriving, flow down, tracing, and prioritizing requirements.
  • Hands-on experiences in using Model-Based Systems Engineering (MBSE) Tools of Cameo and similar tools.
  • Experience with conducting cross-discipline feasibility and trade-off studies to evaluate electronic and mechanical performance from subsystem to system level for the issue
  • Analytical and architectural thinking, system view, physical insight, flexibility, and a hands-on mentality to deliver sustainable results and creative solutions.
  • Strong understanding of Controls and Software development process, including Model-based Design approach and Test-Driven design methodologies.
  • Solid understanding of System Verification and Validation test plan/protocols, executing V&V (Verification and Validation) (Verification and Validation) activities, generating and Analyzing test reports.
  • Understanding of global medical device regulatory environments and clearance
  • Effective communication, computer, documentation, presentation, and interpersonal skills are required, as well as the ability to work both independently and as part of a team.
  • Maintains strict confidentiality of sensitive information.
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.
This role is an office-based role.
About Philips

We are a health technology company. We built our entire company around the belief that every human matters, and we wont 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 .
#LI-PHILIN

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Philips

Healthcare Technology

Amsterdam

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