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Medical Device Development Project Lead (m/f)
Eingestellt von Hays aus Mannheim, Universitätsstadt
Gesuchte Skills: Engineering, Design
Projektbeschreibung
REFERENZNUMMER:
331356/11
IHRE AUFGABEN:
-Deliver project according to plan at project milestones
-Plan and lead technical activities
-Manage technical development activities in collaboration with internal stakeholders as well as in the projects teams
-Lead the collaboration with external development partners
-Monitor work progress according to plan
-Monitor, support and challenge technical development as well as test and verification work
-Monitor development and implementation of manufacturing processes
-Coordinate and monitor technical documentation
IHRE QUALIFIKATIONEN:
-Master degree in Science/Engineering or Mechanical Engineering or university level Engineering education
-Experience in leading packaging/device/combination product projects
-Good understanding of medical device regulations (FDA 21CFR 820, EU Medical Device Directive)
-Experience in product design and design for manufacture
-Experience in managing external suppliers
-Experience in leading device development of parenteral delivery systems, e.g. drug/device combination products with main focus on devices for parenteral administration
-Good communication and conflict solving skills
-Good technical knowledge of primary containers development
-General understanding of human factors engineering and risk management
-Good understanding of clinic studies processes and requirements
-Good understanding of pharmaceutical development in general
-Experience in ophthalmic application device development
-Excellent skills in English are required
WEITERE QUALIFIKATIONEN:
Product manager
331356/11
IHRE AUFGABEN:
-Deliver project according to plan at project milestones
-Plan and lead technical activities
-Manage technical development activities in collaboration with internal stakeholders as well as in the projects teams
-Lead the collaboration with external development partners
-Monitor work progress according to plan
-Monitor, support and challenge technical development as well as test and verification work
-Monitor development and implementation of manufacturing processes
-Coordinate and monitor technical documentation
IHRE QUALIFIKATIONEN:
-Master degree in Science/Engineering or Mechanical Engineering or university level Engineering education
-Experience in leading packaging/device/combination product projects
-Good understanding of medical device regulations (FDA 21CFR 820, EU Medical Device Directive)
-Experience in product design and design for manufacture
-Experience in managing external suppliers
-Experience in leading device development of parenteral delivery systems, e.g. drug/device combination products with main focus on devices for parenteral administration
-Good communication and conflict solving skills
-Good technical knowledge of primary containers development
-General understanding of human factors engineering and risk management
-Good understanding of clinic studies processes and requirements
-Good understanding of pharmaceutical development in general
-Experience in ophthalmic application device development
-Excellent skills in English are required
WEITERE QUALIFIKATIONEN:
Product manager
Projektdetails
Geforderte Qualifikationen
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Kategorie:
Medien/Design, Ingenieurwesen/Technik