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Device Technical Expert – Testing (m/f)
Eingestellt von Hays aus Mannheim, Universitätsstadt
Gesuchte Skills: Design, Engineer
Projektbeschreibung
REFERENZNUMMER:
321792/4
IHRE AUFGABEN:
-Analytical method development, validation and transfer
-Define and document design verification testing, including transport verification testing
-Laboratory activities, testing as well as
planning and leading technical activities -Creating Design Control documentation and contributing to a high quality Design History file
-Definition of product requirements for delivery systems
-Managing technical development activities in collaboration with internal development partners
-Leading the collaboration with external development partners
-Monitor work progress according to plan as well as development and implementation of manufacturing processes
-Monitor, support and challenge technical development as well as test and verification work
-Development and documentation of drug/device combination products and medical devices, including Design Control process and other applicable regulatory, QA and GMP aspects
IHRE QUALIFIKATIONEN:
-Experience in analytical method development for design verification as well as for release testing
-Experience in manufacturing process development and validation
-Experience in mid-early stage activities e.g. design verification testing, design for manufacturing (prototype to model, manufacturing feasibility)
-Experience in late stage activities e.g. tool qualification, equipment qualification
-Knowledge of manufacturing activities e.g. instruction process and DHF compilation
-Experience in testing needed for design verification as well as manufacturing validation
-Good training and presentation skills
-Good technical knowledge of parenteral packaging and medical devices
-Experience of managing external suppliers
WEITERE QUALIFIKATIONEN:
Test engineer
321792/4
IHRE AUFGABEN:
-Analytical method development, validation and transfer
-Define and document design verification testing, including transport verification testing
-Laboratory activities, testing as well as
planning and leading technical activities -Creating Design Control documentation and contributing to a high quality Design History file
-Definition of product requirements for delivery systems
-Managing technical development activities in collaboration with internal development partners
-Leading the collaboration with external development partners
-Monitor work progress according to plan as well as development and implementation of manufacturing processes
-Monitor, support and challenge technical development as well as test and verification work
-Development and documentation of drug/device combination products and medical devices, including Design Control process and other applicable regulatory, QA and GMP aspects
IHRE QUALIFIKATIONEN:
-Experience in analytical method development for design verification as well as for release testing
-Experience in manufacturing process development and validation
-Experience in mid-early stage activities e.g. design verification testing, design for manufacturing (prototype to model, manufacturing feasibility)
-Experience in late stage activities e.g. tool qualification, equipment qualification
-Knowledge of manufacturing activities e.g. instruction process and DHF compilation
-Experience in testing needed for design verification as well as manufacturing validation
-Good training and presentation skills
-Good technical knowledge of parenteral packaging and medical devices
-Experience of managing external suppliers
WEITERE QUALIFIKATIONEN:
Test engineer
Projektdetails
Geforderte Qualifikationen
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Kategorie:
Medien/Design, Ingenieurwesen/Technik