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Embedded Software Medical Device Technical Expert
Eingestellt von Harvey Nash IT Recruitment Switzerland
Gesuchte Skills: Design, Engineering
Projektbeschreibung
For our client in BASEL we are looking for an EMBEDDED SOFTWARE MEDICAL DEVICE TECHNICAL EXPERT for a 6-MONTH contract.
DURATION: 01/10/2018 TO 31/03/2019 (EXTENSION PLANNED)
LOCATION: BASEL
WORKLOAD: 90% - 100%
WE ARE LOOKING FOR A CANDIDATE WHO HAS:
* Excellent technical writing skills (eg, Design Controls)
. Good understanding of medical device regulations (FDA 21CFR 820, EU Medical Device Directive)and of combination products (US) and standards
. Good organization and communication skills in English
. General understanding of Human Factors Engineering and Risk management
. General understanding of pharmaceutical development
MAIN TASKS:
. Lead technical development activities for Embedded software components of medical devices used in combination products, eg auto-injectors, pumps.
. Specify requirements (DIR) of software components and define architecture for future platforms, including liaison with teams developing Digital Ecosystem.
. Working with human factors engineers to define the appropriate HMI and activities.
. Collaborate with electronics experts to ensure appropriate hardware defined for software requirements.
. Manage suppliers in the detailed software design, coding and documentation with consideration of medical device classification.
. Ensuring fail-safe operation through architectural design as well as Real Time error checking to prevent logical, numerical or HMI errors.
. Applying security protocols for wireless communication to pair and operate components of the system.
. Ensuring data security and integrity with consideration of FDA CFR Part 11.
. Planning and reviewing the verification and validation of the software to ensure safe and secure operation with attention to hardware and operating system environment and versions.
. Report in to the Device Project Leader and Delivery System Leader on all technical aspects related to the device development project.
. Generate Design Controls documentation while contributing to a high-quality Design History File (DHF) for parenteral delivery injection systems. Author and Reviewer of DHF documents such as Design Input Requirements, Component Specifications, Design Verification Plan and Verification Summary Report. Ensure quality and compliance to applicable regulations of the DHF elements of the assigned projects.
. Ensure device design development in compliance with the regulations and delivered to a high quality.
. Root cause analysis of out-of-specification product and develop robust solutions to prevent re-occurrence.
For further details please contact Beata Arciszewska:
email: (see below)
DURATION: 01/10/2018 TO 31/03/2019 (EXTENSION PLANNED)
LOCATION: BASEL
WORKLOAD: 90% - 100%
WE ARE LOOKING FOR A CANDIDATE WHO HAS:
* Excellent technical writing skills (eg, Design Controls)
. Good understanding of medical device regulations (FDA 21CFR 820, EU Medical Device Directive)and of combination products (US) and standards
. Good organization and communication skills in English
. General understanding of Human Factors Engineering and Risk management
. General understanding of pharmaceutical development
MAIN TASKS:
. Lead technical development activities for Embedded software components of medical devices used in combination products, eg auto-injectors, pumps.
. Specify requirements (DIR) of software components and define architecture for future platforms, including liaison with teams developing Digital Ecosystem.
. Working with human factors engineers to define the appropriate HMI and activities.
. Collaborate with electronics experts to ensure appropriate hardware defined for software requirements.
. Manage suppliers in the detailed software design, coding and documentation with consideration of medical device classification.
. Ensuring fail-safe operation through architectural design as well as Real Time error checking to prevent logical, numerical or HMI errors.
. Applying security protocols for wireless communication to pair and operate components of the system.
. Ensuring data security and integrity with consideration of FDA CFR Part 11.
. Planning and reviewing the verification and validation of the software to ensure safe and secure operation with attention to hardware and operating system environment and versions.
. Report in to the Device Project Leader and Delivery System Leader on all technical aspects related to the device development project.
. Generate Design Controls documentation while contributing to a high-quality Design History File (DHF) for parenteral delivery injection systems. Author and Reviewer of DHF documents such as Design Input Requirements, Component Specifications, Design Verification Plan and Verification Summary Report. Ensure quality and compliance to applicable regulations of the DHF elements of the assigned projects.
. Ensure device design development in compliance with the regulations and delivered to a high quality.
. Root cause analysis of out-of-specification product and develop robust solutions to prevent re-occurrence.
For further details please contact Beata Arciszewska:
email: (see below)
Projektdetails
Geforderte Qualifikationen
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Kategorie:
Medien/Design, Ingenieurwesen/Technik