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Medical Device Senior Technical Expert (m/f)
Eingestellt von Hays aus Mannheim, Universitätsstadt
Gesuchte Skills: Engineering, Design
Projektbeschreibung
REFERENZNUMMER:
324433/11
IHRE AUFGABEN:
-Compile Design Control documentation and contribute to a high quality Design History file
-Author and review of design history file relevant documents
-Ensure quality and compliance to applicable regulations of the DHF elements of the assigned projects
-Ensure device design development in compliance of the regulations and at high quality
-Advise on the development and/or optimization of the manufacturing processes for medical devices and combination products
-Plan and lead technical activities
-Manage technical development activities in collaboration with internal development partners
-Lead or contribute to risk management activities
-Support in Human Factors Engineering activities
-Review of medical device and/or packaging-related testing documents
IHRE QUALIFIKATIONEN:
-Senior expert in medical device development and combination products
-Knowledge about devices (e.g. syringe, auto-injectors etc.)
-Knowledge about combination products desirable
-Master degree in science/engineering or mechanical engineering or university level engineering education
-Excellent English skills
WEITERE QUALIFIKATIONEN:
Project assistant, Regulatory affairs manager
324433/11
IHRE AUFGABEN:
-Compile Design Control documentation and contribute to a high quality Design History file
-Author and review of design history file relevant documents
-Ensure quality and compliance to applicable regulations of the DHF elements of the assigned projects
-Ensure device design development in compliance of the regulations and at high quality
-Advise on the development and/or optimization of the manufacturing processes for medical devices and combination products
-Plan and lead technical activities
-Manage technical development activities in collaboration with internal development partners
-Lead or contribute to risk management activities
-Support in Human Factors Engineering activities
-Review of medical device and/or packaging-related testing documents
IHRE QUALIFIKATIONEN:
-Senior expert in medical device development and combination products
-Knowledge about devices (e.g. syringe, auto-injectors etc.)
-Knowledge about combination products desirable
-Master degree in science/engineering or mechanical engineering or university level engineering education
-Excellent English skills
WEITERE QUALIFIKATIONEN:
Project assistant, Regulatory affairs manager
Projektdetails
Geforderte Qualifikationen
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Kategorie:
Medien/Design, Ingenieurwesen/Technik