Philips
Systems Test Engineer – Product Safety(m/w/x)
Full-timeOn-siteSenior
Böblingen
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PHPhilips
Systems Test Engineer – Product Safety(m/w/x)
Böblingen
Full-timeOn-siteSenior
Nejo AI Summary
Overseeing regulatory compliance for patient monitoring devices. Deep knowledge of IEC 60601-1 and FDA/UL regulations for patient monitoring devices required. Work with global impact on 3 billion lives.
Requirements
- At least 5-10 years of industry experience
- Deep knowledge of product safety standards (IEC 60601-1, IEC60601-1-x, IEC/ISO 60601-2-xx, IEC/ISO80601-2-xx)
- Deep knowledge of relevant regulations (UL, FDA, CSA, IEC, GB)
- Experience with patient monitoring devices
- Knowhow of design control processes for medical device design
- System thinking mindset and domain expertise
- Ability to manage and prioritize multiple projects
- Outstanding communication skills
- Proven leadership in project management
- International perspective and eagerness to collaborate
- Structured and self-organized
- Good team player and ability to work independently
Tasks
- Serve as the subject matter expert on product safety standards
- Lead and manage complex system testing projects
- Ensure compliance with safety and regulatory requirements
- Act as the primary liaison with external safety test agencies
- Develop and maintain documentation of test procedures and results
- Guide cross-functional teams in integrating product safety considerations
Work Experience
- 5 - 10 years
Education
- Bachelor's degreeOR
- Master's degree
Languages
- English – Business Fluent
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Philips and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
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PHPhilips
Systems Test Engineer – Product Safety(m/w/x)
Böblingen
Full-timeOn-siteSenior
Nejo AI Summary
Overseeing regulatory compliance for patient monitoring devices. Deep knowledge of IEC 60601-1 and FDA/UL regulations for patient monitoring devices required. Work with global impact on 3 billion lives.
Requirements
- At least 5-10 years of industry experience
- Deep knowledge of product safety standards (IEC 60601-1, IEC60601-1-x, IEC/ISO 60601-2-xx, IEC/ISO80601-2-xx)
- Deep knowledge of relevant regulations (UL, FDA, CSA, IEC, GB)
- Experience with patient monitoring devices
- Knowhow of design control processes for medical device design
- System thinking mindset and domain expertise
- Ability to manage and prioritize multiple projects
- Outstanding communication skills
- Proven leadership in project management
- International perspective and eagerness to collaborate
- Structured and self-organized
- Good team player and ability to work independently
Tasks
- Serve as the subject matter expert on product safety standards
- Lead and manage complex system testing projects
- Ensure compliance with safety and regulatory requirements
- Act as the primary liaison with external safety test agencies
- Develop and maintain documentation of test procedures and results
- Guide cross-functional teams in integrating product safety considerations
Work Experience
- 5 - 10 years
Education
- Bachelor's degreeOR
- Master's degree
Languages
- English – Business Fluent
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Philips and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
About the Company
Philips
Industry
Healthcare
Description
Das Unternehmen trägt durch innovative Lösungen zur Verbesserung der Lebensqualität von 3 Milliarden Menschen bei.
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