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Product Development Engineer: EU MDD, FDA, PAL, Engineer, CAD
Eingestellt von Sentinel IT LLP
Gesuchte Skills: Engineer, Engineering, Cad, Design
Projektbeschreibung
Product Development Engineer: EU MDD, FDA, PAL, Engineer, CAD, Implants, German
I have a great opportunity for a product development engineer to work for an innovative and ground breaking medical device company on an exciting long term freelance basis in Switzerland. the project is currently running until the end of 2015 but it potentially could get extended (due to the size/scope of the work), right up until the end of 2016! I am looking for a GERMAN/ENGLISH speaker for this role.
Please find details of the role below:
In this position you will:
- be responsible for technical engineering support of different initiatives driven by manufacturing (transfers, harmonization, process changes, etc.).
- update registration relevant documentation of the Design History File to meet current standards and requirements (eg risk management documents, functional & design requirements, verification & validation activities).
- technically lead optimizations and design changes and ensure proper communication and timing with manufacturing and shared services.
- collaborate with the technical engineering office, write test methods and setups, complete testing requirements and write verification & validation reports.
Information exchange and collaboration between internal, local, external and foreign partners is essential. Close cooperation with internal departments, domestic and international authorities as well as the conscientious preparation of the required documents ensures compliance with Medical Device Regulations (EU MDD, US FDA, JP PAL).
Product Development Engineer: EU MDD, FDA, PAL, Engineer, CAD, Implants, German
I have a great opportunity for a product development engineer to work for an innovative and ground breaking medical device company on an exciting long term freelance basis in Switzerland. the project is currently running until the end of 2015 but it potentially could get extended (due to the size/scope of the work), right up until the end of 2016! I am looking for a GERMAN/ENGLISH speaker for this role.
Please find details of the role below:
In this position you will:
- be responsible for technical engineering support of different initiatives driven by manufacturing (transfers, harmonization, process changes, etc.).
- update registration relevant documentation of the Design History File to meet current standards and requirements (eg risk management documents, functional & design requirements, verification & validation activities).
- technically lead optimizations and design changes and ensure proper communication and timing with manufacturing and shared services.
- collaborate with the technical engineering office, write test methods and setups, complete testing requirements and write verification & validation reports.
Information exchange and collaboration between internal, local, external and foreign partners is essential. Close cooperation with internal departments, domestic and international authorities as well as the conscientious preparation of the required documents ensures compliance with Medical Device Regulations (EU MDD, US FDA, JP PAL).
Product Development Engineer: EU MDD, FDA, PAL, Engineer, CAD, Implants, German
Projektdetails
Geforderte Qualifikationen
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Kategorie:
Medien/Design, Ingenieurwesen/Technik