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Medical Device Technical Expert - Human Factor, Switzerland
Eingestellt von Michael Bailey Associates - UK Contracts
Gesuchte Skills: Engineering, Usability, Design, Engineer
Projektbeschreibung
For our Life Sciences client in Switzerland, we care seeking for a Medical Device Senior Technical Expert - Human factor.
JOB TITLE: MEDICAL DEVICE TECHNICAL EXPERT - HUMAN FACTOR
START DATE: 02/01/2017
END DATE: 30/06/2017
LOCATION: Basel, Switzerland
LANGUAGE: Excellent skills in English, verbal and written are required. Other language skills, eg French, German are advantageous.
YOUR ROLE:
- The Human Factors Engineer will be responsible for independently leading the planning, execution and reporting of human factors studies and user interface design, according to current regulations and guidelines within the medical device and pharmaceutical industries.
- Performs anthropometric, biomechanical, ergonomic, and systems safety analyses to identify and assess risk in product development.
- Cross-examines and optimizes developmental prototypes and provides ergonomic, usability and safety assessments for consumer healthcare products, medical devices and pharmaceutical packaging.
- Leads IFU design and development including validation.
- Supporting Human Factors related documentation for Health Authority registration in collaboration with Drug Regulatory Affairs.
YOUR EXPERIENCE:
Minimum requirements:
- Bachelor's or Master degree in engineering, ergonomics, human factors, usability or related discipline.
- At least 3 years of experience in applying Human Factors Engineering to medical devices development, preferably in the pharmaceutical industry, including.
- 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.
- Proven track record of successfully managing interfaces to other functions.
- Experience in managing external suppliers for user studies (formative and summative studies)
- Good understanding of the risk management activities
We welcome applications of consultants' who match most of the above requirements and are available on a short notice. There is a competitive Hourly rate available for the contract; alternative market rates are also welcome.
We hope that the role will be of interest to you and understand that further information may be required prior to an application to the end client, please feel free to email or call me at anytime with any questions you may have.
Looking forward to hear from you soon,
Kind regards,
Neha Sharma
Pharmaceutical & Life Sciences Business Developer
Recruiting Team MBA,
Michael Bailey Associates
Michael Bailey International is acting as an Employment Business in relation to this vacancy.
JOB TITLE: MEDICAL DEVICE TECHNICAL EXPERT - HUMAN FACTOR
START DATE: 02/01/2017
END DATE: 30/06/2017
LOCATION: Basel, Switzerland
LANGUAGE: Excellent skills in English, verbal and written are required. Other language skills, eg French, German are advantageous.
YOUR ROLE:
- The Human Factors Engineer will be responsible for independently leading the planning, execution and reporting of human factors studies and user interface design, according to current regulations and guidelines within the medical device and pharmaceutical industries.
- Performs anthropometric, biomechanical, ergonomic, and systems safety analyses to identify and assess risk in product development.
- Cross-examines and optimizes developmental prototypes and provides ergonomic, usability and safety assessments for consumer healthcare products, medical devices and pharmaceutical packaging.
- Leads IFU design and development including validation.
- Supporting Human Factors related documentation for Health Authority registration in collaboration with Drug Regulatory Affairs.
YOUR EXPERIENCE:
Minimum requirements:
- Bachelor's or Master degree in engineering, ergonomics, human factors, usability or related discipline.
- At least 3 years of experience in applying Human Factors Engineering to medical devices development, preferably in the pharmaceutical industry, including.
- 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.
- Proven track record of successfully managing interfaces to other functions.
- Experience in managing external suppliers for user studies (formative and summative studies)
- Good understanding of the risk management activities
We welcome applications of consultants' who match most of the above requirements and are available on a short notice. There is a competitive Hourly rate available for the contract; alternative market rates are also welcome.
We hope that the role will be of interest to you and understand that further information may be required prior to an application to the end client, please feel free to email or call me at anytime with any questions you may have.
Looking forward to hear from you soon,
Kind regards,
Neha Sharma
Pharmaceutical & Life Sciences Business Developer
Recruiting Team MBA,
Michael Bailey Associates
Michael Bailey International is acting as an Employment Business in relation to this vacancy.
Projektdetails
Geforderte Qualifikationen
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Kategorie:
Medien/Design, Ingenieurwesen/Technik