Dieses Jobangebot ist archiviert und steht nicht mehr zur Verfügung.
Vakante Jobangebote finden Sie unter Projekte.
Vakante Jobangebote finden Sie unter Projekte.
Human Factors Engineer (m/f)
Eingestellt von Hays aus Mannheim, Universitätsstadt
Gesuchte Skills: Engineering, Design, Usability, Engineer
Projektbeschreibung
REFERENZNUMMER:
352223/11
IHRE AUFGABEN:
-Provide human factors support throughout the product development lifecycle including user needs identification, development of user profiles and use scenarios, task analysis, use-related risk analysis, generation of hardware and software design concepts
-Plan and execute formative and summative user studies, reporting and presenting design recommendations to the project team
-Define appropriate sample sizes and statistical methods for analysis
-Perform anthropometric, biomechanical, ergonomic, and systems safety analyses to identify and assess risk in product development
-Cross-examine and optimize developmental prototypes and provide ergonomic, usability and safety assessments for consumer healthcare products, medical devices and pharmaceutical packaging
-Lead IFU design and development including validation
-Closely collaborate with cross functional stakeholders (e.g. risk management, Drug Regulatory Affairs, clinical development)
-Supporting Human Factors related documentation for Health Authority registration in collaboration with Drug Regulatory Affairs
-Work independently against self-set targets when necessary
-Management of external vendors
IHRE QUALIFIKATIONEN:
-Bachelor’s or Master degree in engineering, ergonomics, human factors, usability or related discipline
-Excellent skills in English, verbal and written are required, other language skills are advantageous
-Profound experience in applying Human Factors Engineering to medical devices development, preferably in the pharmaceutical industry
-Good understanding of medical devices development processes in general
-Specific knowledge on applying Human Factors Engineering processes to medical device development from concept generation to health authority submission
-Experience in project/program management
-Experience in developing and documenting Human Factors activities for medical devices as required by regulation
-Experience in managing external suppliers for user studies (formative and summative studies)
-Good communication and problem solving in the team and across organizational boundaries
WEITERE QUALIFIKATIONEN:
Project manager
352223/11
IHRE AUFGABEN:
-Provide human factors support throughout the product development lifecycle including user needs identification, development of user profiles and use scenarios, task analysis, use-related risk analysis, generation of hardware and software design concepts
-Plan and execute formative and summative user studies, reporting and presenting design recommendations to the project team
-Define appropriate sample sizes and statistical methods for analysis
-Perform anthropometric, biomechanical, ergonomic, and systems safety analyses to identify and assess risk in product development
-Cross-examine and optimize developmental prototypes and provide ergonomic, usability and safety assessments for consumer healthcare products, medical devices and pharmaceutical packaging
-Lead IFU design and development including validation
-Closely collaborate with cross functional stakeholders (e.g. risk management, Drug Regulatory Affairs, clinical development)
-Supporting Human Factors related documentation for Health Authority registration in collaboration with Drug Regulatory Affairs
-Work independently against self-set targets when necessary
-Management of external vendors
IHRE QUALIFIKATIONEN:
-Bachelor’s or Master degree in engineering, ergonomics, human factors, usability or related discipline
-Excellent skills in English, verbal and written are required, other language skills are advantageous
-Profound experience in applying Human Factors Engineering to medical devices development, preferably in the pharmaceutical industry
-Good understanding of medical devices development processes in general
-Specific knowledge on applying Human Factors Engineering processes to medical device development from concept generation to health authority submission
-Experience in project/program management
-Experience in developing and documenting Human Factors activities for medical devices as required by regulation
-Experience in managing external suppliers for user studies (formative and summative studies)
-Good communication and problem solving in the team and across organizational boundaries
WEITERE QUALIFIKATIONEN:
Project manager
Projektdetails
Geforderte Qualifikationen
-
Kategorie:
Medien/Design, Ingenieurwesen/Technik