System Engineer - Medical Devices

Job Title

Job Description

The Supplier Transfer Excellence System Engineer is responsible for meticulously testing system integration and functionality, ensuring adherence to technical specifications and project requirements, developing comprehensive test designs and protocols, and facilitating seamless supplier transfer with a focus on operational efficiency and reliability across all components. The role executes tests using a risk-based approach to validate functionality against design input requirements and formalizes findings in documented reports. The role compiles data on release readiness and quality assessment to evaluate seamless supplier transitions. The role ensures comprehensive and up-to-date documentation of test plans, protocols, and reports using structured methods and tools.

Your role:

• Collaborate across functions to refine problem scopes and third-party integration ideas

• Evaluate interdisciplinary impacts on design, usability, reliability, power, and performance

• Shape subsystem requirements and ensure alignment with system architecture and design standards

• Conduct feasibility studies, technical maturity assessments, and risk analyses

• Define test scopes and oversee Design Verification & Validation documentation

• Ensure compliance with regulations, standards, and safety requirements

• Report risks, readiness, and go/no-go recommendations to stakeholders

• Partner with project managers on scope definition and work planning

• Ensure documentation aligns with QMS and regulatory standards

• Support modular integration, trace progress, and stay current with technical trends

You're the right fit if you have :

• BE/BTech/ME/M-Tech in Electrical & Electronics Engineering from a reputed institute

• 5 to 7 years of Analog & Digital engineering experience with solid system engineering & system integration understanding

Technical Skills:

• Hands-on experience with tools like Track Wise, Clear-quest, Windchill, DOORs or equivalent will be an added advantage

• 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

• New Product Introduction (NPI) and Product Life Cycle Management

• Quality mindset in design and documentation 

Soft Skills:

• 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 

• Global and Cross-functional Experience/Skills in a Matrix Organization will be an added advantage

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 is an office 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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