R&D Engineer Medical Devices (m/f/d)
Permanent
About Heraeus
Making displays foldable Helping hearts beat with medical innovations Or breathing new life into precious metals As a family-owned global technology group we help our customers to always being one step ahead.
About Heraeus Medevio
Together we improve lives. At Heraeus Medevio we bring lifesaving and life-changing medical devices to market through partnerships with medical device manufacturing companies. Backed by Heraeus Group we are committed to the growth of our teams and organization by providing an open space for open minds.
To reach our vision of improving 100 million lives every year we foster a culture of curiosity that thrives on challenge continuous learning growth and the opportunity to try new things. With sites in the United States European Union and Asia and over 2200 employees worldwide together we will meet tomorrows challenges today.
The following challenges await you:
In this role you will contribute to the development of interventional medical devices that enhance patient safety and therapeutic outcomes worldwide. Your key responsibilities include:
- Contribute to customerspecific product development projects from concept freeze through detailed design and transfer to manufacturing.
- Working in many areas of interventional devices including access devices advanced diagnostic and therapeutic catheters and complex delivery systems applying state-of-the-art technology.
- Working collaboratively in crossfunctional and international teams including program managers design and process engineers prototyping specialists and RA/QA representativesas well as with external business partners and customers.
- Developing and building prototypesboth at the conceptual drafting stage and handsonaligned with safety usability and clinical performance requirements.
- Developing test methods for design verification and simulateduse validation defining manufacturing processes and documenting all work in our paperless PLM environment.
- Ensuring full and compliant documentation according to regulatory frameworks standards and industry best practices under our design control policies.
Your profile
- Bachelors degree in a scientific or engineering discipline with a focus on Mechanical Plastics or Biomedical Engineering; an advanced degree is preferred.
- Minimum of 3 years of experience in the interventional device industry.
- Strong technical expertise in medical devices applied materials functional product design designformanufacturability and prototyping.
- Excellent communication skills in English both written and spoken.
- Familiarity with Good Documentation Practice Design Control and relevant standards such as ISO 13485 and FDA requirements.
- Willingness to travel occasionally to customers or clinical study locations worldwide.
Curious Apply now!
We are interested in finding the best candidates and they may come from a nontraditional background. So please dont hesitate to apply even if you arent an exact fit. We look forward to getting you started on your employment journey with Heraeus Medevio!
Any further questions
Our Recruiting Team Heraeus Medevio is happy to assist you by email: . Or visit us at .
Required Experience:
IC
R&D Engineer Medical Devices (m/f/d)PermanentAbout HeraeusMaking displays foldable Helping hearts beat with medical innovations Or breathing new life into precious metals As a family-owned global technology group we help our customers to always being one step ahead.About Heraeus MedevioTogether we i...
R&D Engineer Medical Devices (m/f/d)
Permanent
About Heraeus
Making displays foldable Helping hearts beat with medical innovations Or breathing new life into precious metals As a family-owned global technology group we help our customers to always being one step ahead.
About Heraeus Medevio
Together we improve lives. At Heraeus Medevio we bring lifesaving and life-changing medical devices to market through partnerships with medical device manufacturing companies. Backed by Heraeus Group we are committed to the growth of our teams and organization by providing an open space for open minds.
To reach our vision of improving 100 million lives every year we foster a culture of curiosity that thrives on challenge continuous learning growth and the opportunity to try new things. With sites in the United States European Union and Asia and over 2200 employees worldwide together we will meet tomorrows challenges today.
The following challenges await you:
In this role you will contribute to the development of interventional medical devices that enhance patient safety and therapeutic outcomes worldwide. Your key responsibilities include:
- Contribute to customerspecific product development projects from concept freeze through detailed design and transfer to manufacturing.
- Working in many areas of interventional devices including access devices advanced diagnostic and therapeutic catheters and complex delivery systems applying state-of-the-art technology.
- Working collaboratively in crossfunctional and international teams including program managers design and process engineers prototyping specialists and RA/QA representativesas well as with external business partners and customers.
- Developing and building prototypesboth at the conceptual drafting stage and handsonaligned with safety usability and clinical performance requirements.
- Developing test methods for design verification and simulateduse validation defining manufacturing processes and documenting all work in our paperless PLM environment.
- Ensuring full and compliant documentation according to regulatory frameworks standards and industry best practices under our design control policies.
Your profile
- Bachelors degree in a scientific or engineering discipline with a focus on Mechanical Plastics or Biomedical Engineering; an advanced degree is preferred.
- Minimum of 3 years of experience in the interventional device industry.
- Strong technical expertise in medical devices applied materials functional product design designformanufacturability and prototyping.
- Excellent communication skills in English both written and spoken.
- Familiarity with Good Documentation Practice Design Control and relevant standards such as ISO 13485 and FDA requirements.
- Willingness to travel occasionally to customers or clinical study locations worldwide.
Curious Apply now!
We are interested in finding the best candidates and they may come from a nontraditional background. So please dont hesitate to apply even if you arent an exact fit. We look forward to getting you started on your employment journey with Heraeus Medevio!
Any further questions
Our Recruiting Team Heraeus Medevio is happy to assist you by email: . Or visit us at .
Required Experience:
IC
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