PHILIPS Hiring Biomedical Development Engineer in Across Global Salary starts from 2,28,000$/year Apply Online

Company:	PHILIPS
Job Role:	Biomedical Development Engineer.
Experience:	(1-3 years).
Vacancy:	10+
Qualification:	BE/B.Tech, ME/M.Tech, MS , PhD, In Biomedical Or Related Degree.
Salary:	2,28,000$/year.
Location:	Across Global.
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Apply Mode:	(Online)
Deadline:	Not Mentioned

About the Company:

Philips began as a small company in Eindhoven, over 125 years ago. The founders had no idea it would become the driving force behind global innovation, dedicated to improving millions of lives worldwide. However, it did.

Philips is today one of the world's leading health technology companies, committed to improving life for people around the world. Our enthusiasm, inspiration, collaboration, and diversity are what will enable us to deliver on this promise.

We have over 80,000 talented people in over 100 countries, and we are always seeking more. A healthy, more connected world requires like-minded, motivated, focused minds to transform themselves personally and professionally while creating a healthier society.

Having a job at Philips means more than just working. You will gain lasting and positive transformations from this experience full of unexpected moments. Assist us in making the world a better place while building a career you could never have imagined. You as well.

Job Description:

In this role, you have the opportunity to:

• Your responsibility as the Development Engineer at Compass Venture is to design, check, optimize, integrate, manage life cycles, and verify (elements, parts, and a complete solution) products, systems, and software.
• Your work is developed based on business and user requirements, compliance, quality, and cost considerations. As well as develop detailed designs according to Philips reference architecture requirements and product requirements.
• Engineering developers combine purchased and/or existing parts and elements into (elements of) products, systems, and/or solutions. Verifies the developed elements and parts according to verification plans, and finalizes the design and integration.
• Further, the design is tested, analyzed, and verified.
• It is expected that you will approach the designs created from the outside in. During the planning process, you will deliver input to the system architect or venture manager.
• Using a structured and methodical approach, you'll be able to prepare personal schedules and progress reports.
• I2M processes provide templates that must be followed for documentation.

  To succeed in this role, you should have the following skills and experience:

• PhD in Biomedical Engineering
• 3+ years of relevant experience in verification, validation, and supply chain management of new medical products.
• The ability to create partly and sometimes wholly new products, processes, or technologies where the objective may not be clear.
• Compelling skills for the role include: planning and aligning, managing conflict, adapting to changing situations, and collaborating
• The Netherlands and England.

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