Philips
Safety Risk Engineer(m/w/x)
Full-timeWith HomeofficeExperienced
Böblingen
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PHPhilips Medizin Systeme Böblingen GmbH
Engineering Responsible Manager/Technical Product Owner(m/w/x)
Böblingen
Full-timeWith Home OfficeExperienced
Nejo AI Summary
Managing design documentation and compliance for emergency and intensive care patient monitoring systems at a global medical device manufacturer. Experience with medical technology products in regulated industry, especially IEC 60601-1, required. Direct responsibility for product compliance in global medical device audits.
Requirements
- Degree in engineering, preferably electrical engineering
- Several years of professional experience with medical technology products
- Very good understanding and experience in regulated industry
- Good understanding of external standards, especially IEC 60601-1
- Very high level of quality awareness
- High ability to self-organize
- Experience in project management of smaller projects in cross-functional teams
- German language skills
Tasks
- Own the product design documentation
- Ensure compliance of product documents with internal specifications
- Maintain traceability of requirements within change frameworks
- Represent the product in internal and external audits
- Verify that changes do not negatively impact product quality
- Lead problem-solving discussions with experts
- Participate in product-related CAPAs
Work Experience
- approx. 1 - 4 years
Education
- Bachelor's degree
Languages
- German – Business Fluent
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Philips Medizin Systeme Böblingen GmbH 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 Medizin Systeme Böblingen GmbH
Engineering Responsible Manager/Technical Product Owner(m/w/x)
Böblingen
Full-timeWith Home OfficeExperienced
Nejo AI Summary
Managing design documentation and compliance for emergency and intensive care patient monitoring systems at a global medical device manufacturer. Experience with medical technology products in regulated industry, especially IEC 60601-1, required. Direct responsibility for product compliance in global medical device audits.
Requirements
- Degree in engineering, preferably electrical engineering
- Several years of professional experience with medical technology products
- Very good understanding and experience in regulated industry
- Good understanding of external standards, especially IEC 60601-1
- Very high level of quality awareness
- High ability to self-organize
- Experience in project management of smaller projects in cross-functional teams
- German language skills
Tasks
- Own the product design documentation
- Ensure compliance of product documents with internal specifications
- Maintain traceability of requirements within change frameworks
- Represent the product in internal and external audits
- Verify that changes do not negatively impact product quality
- Lead problem-solving discussions with experts
- Participate in product-related CAPAs
Work Experience
- approx. 1 - 4 years
Education
- Bachelor's degree
Languages
- German – Business Fluent
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Philips Medizin Systeme Böblingen GmbH 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 Medizin Systeme Böblingen GmbH
Industry
Healthcare
Description
Das Unternehmen entwickelt und produziert Patientenüberwachungssysteme für den weltweiten Markt, insbesondere in der Notfall- und Intensivmedizin.
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