Biomedical Engineer with Visa Sponsorship

About the Company

Philips is a global leader in health technology, focused on improving people’s health and enabling better outcomes across the health continuum from healthy living and prevention, to diagnosis, treatment and home care. With a century of innovation, Philips harnesses advanced technology and deep clinical and consumer insights to deliver integrated solutions. Our purpose is to improve the lives of 2.5 billion people a year by 2030, through meaningful innovation. We are committed to fostering an inclusive and diverse workplace where every individual can thrive and contribute to our mission.

Job Description

We are seeking a highly motivated and skilled Biomedical Engineer to join our innovative R&D team in Seattle, WA. This is an exceptional opportunity for an experienced engineer to contribute to the development of cutting-edge medical devices and solutions that transform healthcare. As a Biomedical Engineer at Philips, you will play a crucial role in the design, development, testing, and implementation of new products, working closely with cross-functional teams including software, hardware, clinical, and regulatory experts. This position requires a strong understanding of engineering principles applied to biological systems and a passion for improving patient outcomes through technology. We are proud to offer visa sponsorship for qualified international candidates.

Key Responsibilities

• Design, develop, and test medical devices and systems, ensuring compliance with regulatory standards.
• Conduct research and analysis to identify and evaluate new technologies and materials for product improvement.
• Collaborate with clinical specialists and product managers to define user requirements and translate them into technical specifications.
• Perform risk analysis, FMEA, and verification/validation activities for medical devices.
• Participate in all phases of the product development lifecycle, from concept to commercialization.
• Document design specifications, test protocols, and reports accurately and thoroughly.
• Provide technical support for existing products and assist in troubleshooting and problem resolution.
• Mentor junior engineers and contribute to a culture of continuous learning and innovation.

Required Skills

• Bachelor's or Master's degree in Biomedical Engineering, Electrical Engineering, Mechanical Engineering, or a related field.
• 4+ years of experience in medical device development or a highly regulated industry.
• Proficiency in CAD software (e.g., SolidWorks, AutoCAD).
• Strong understanding of medical device regulations (e.g., FDA, MDR, ISO 13485).
• Experience with risk management tools and processes (e.g., FMEA).
• Proven ability to work effectively in cross-functional teams.
• Excellent problem-solving, analytical, and communication skills.
• Demonstrated experience in design control and product lifecycle management.

Preferred Qualifications

• Ph.D. in Biomedical Engineering or a related discipline.
• Experience with specific medical device technologies such as imaging systems, patient monitoring, or diagnostic equipment.
• Familiarity with programming languages (e.g., Python, MATLAB) for data analysis and prototyping.
• Certified Professional for Medical Software (CPMS) or similar certification.
• Experience with biological signal processing or biomechanics.
• Previous experience in a global R&D environment.

Perks & Benefits

• Comprehensive health, dental, and vision insurance.
• Generous paid time off and holidays.
• 401(k) matching and retirement planning.
• Tuition reimbursement and professional development opportunities.
• Employee wellness programs and on-site fitness facilities.
• Parental leave and family support programs.
• Opportunity to work on life-changing healthcare innovations.
• Relocation assistance and visa sponsorship provided.

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