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Human Factors Engineer
Eingestellt von RM IT Professional Resources AG
Gesuchte Skills: Engineering, Design, Engineer, Usability
Projektbeschreibung
Human Factors Engineer with good understanding of medical devices development processes wanted for our Basel based client in the pharmaceutical sector.
YOUR EXPERIENCE/SKILLS:
- University Degree in Engineering, Ergonomics, Human Factors, Usability or in a related area with good understanding of medical devices development processes in general
- At least 8 years' experience in applying Human Factors Engineering to medical devices development, preferably in the pharmaceutical industry
- Specific knowledge on applying Human Factors Engineering processes to medical device development from concept generation to health authority submission
- Expertise in Project/Program management as well as Risk management and in developing and documenting Human Factors activities for medical devices as required by regulation
- Proven track record of successfully managing interfaces to other functions along with experience in managing external suppliers for user studies (formative and summative studies)
Languages: fluent English both written and spoken, knowledge in French and German advantageous
YOUR TASKS:
- Providing human factors support throughout the product development life cycle including user needs identification, development of user profiles and use scenarios, etc.
- Organising and managing formative and summative user studies as well as reporting and presenting design recommendations to the project team
- Cross-examining and suggesting design optimisation to enhance ergonomic, usability and safety as well as leading IFU design and development
- Liaising with cross-functional stakeholders like Risk management, Drug Regulatory Affairs, clinical development, etc.
- Assisting Human Factors related documentation for Health Authority registration in collaboration with Drug Regulatory Affairs
- Managing external vendors and working against self-targets
START: ASAP
DURATION: 6MM+
LOCATION: Basel, Switzerland
REF.NR.: BH10817
Does this sound like an interesting and challenging opportunity to you?
Then take the next step by sending us your CV as a Word document and a contact telephone number.
DUE TO WORK PERMIT RESTRICTIONS WE CAN UNFORTUNATELY ONLY CONSIDER APPLICATIONS FROM EU OR SWISS CITIZENS AS WELL AS CURRENT WORK-PERMIT HOLDERS FOR SWITZERLAND.
GOING THE EXTRA MILE
NEW TO SWITZERLAND?
In case of successful placement, we support you with:
- All administrative questions
- Finding an apartment
- Health - and social insurance
- Work permit and much more
YOUR EXPERIENCE/SKILLS:
- University Degree in Engineering, Ergonomics, Human Factors, Usability or in a related area with good understanding of medical devices development processes in general
- At least 8 years' experience in applying Human Factors Engineering to medical devices development, preferably in the pharmaceutical industry
- Specific knowledge on applying Human Factors Engineering processes to medical device development from concept generation to health authority submission
- Expertise in Project/Program management as well as Risk management and in developing and documenting Human Factors activities for medical devices as required by regulation
- Proven track record of successfully managing interfaces to other functions along with experience in managing external suppliers for user studies (formative and summative studies)
Languages: fluent English both written and spoken, knowledge in French and German advantageous
YOUR TASKS:
- Providing human factors support throughout the product development life cycle including user needs identification, development of user profiles and use scenarios, etc.
- Organising and managing formative and summative user studies as well as reporting and presenting design recommendations to the project team
- Cross-examining and suggesting design optimisation to enhance ergonomic, usability and safety as well as leading IFU design and development
- Liaising with cross-functional stakeholders like Risk management, Drug Regulatory Affairs, clinical development, etc.
- Assisting Human Factors related documentation for Health Authority registration in collaboration with Drug Regulatory Affairs
- Managing external vendors and working against self-targets
START: ASAP
DURATION: 6MM+
LOCATION: Basel, Switzerland
REF.NR.: BH10817
Does this sound like an interesting and challenging opportunity to you?
Then take the next step by sending us your CV as a Word document and a contact telephone number.
DUE TO WORK PERMIT RESTRICTIONS WE CAN UNFORTUNATELY ONLY CONSIDER APPLICATIONS FROM EU OR SWISS CITIZENS AS WELL AS CURRENT WORK-PERMIT HOLDERS FOR SWITZERLAND.
GOING THE EXTRA MILE
NEW TO SWITZERLAND?
In case of successful placement, we support you with:
- All administrative questions
- Finding an apartment
- Health - and social insurance
- Work permit and much more
Projektdetails
Geforderte Qualifikationen
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Kategorie:
Medien/Design, Ingenieurwesen/Technik