Dieses Jobangebot ist archiviert und steht nicht mehr zur Verfügung.
Vakante Jobangebote finden Sie unter Projekte.
Vakante Jobangebote finden Sie unter Projekte.
Medical Device Technical Expert
Eingestellt von RM IT Professional Resources AG
Gesuchte Skills: Design, Engineering
Projektbeschreibung
Medical Device Technical Expert wanted for our Basel based client in the pharmaceutical sector.
YOUR EXPERIENCE/SKILLS:
- 8+ years' experience in software development with main focus on medical devices for parenteral administration and generating DHF documentation, including designing input requirements, technical specifications, design verification, validation, and transfer.
- Excellent technical writing skills, ideally in Design Controls
- Good understanding of medical device regulations, such as FDA 21CFR 820 and EU Medical Device Directive coupled with combination products (US) and standards
- General understanding of Pharmaceutical Development, Human Factors Engineering and Risk management
- Good organisation and communication skills
- Languages: fluent English both written and spoken
YOUR TASKS:
- Specifying requirements of software components and defining architecture for future platforms
- Collaborating with human factors engineers and electronics experts to ensure appropriate hardware defined for software requirements
- Ensuring data security and integrity as well as fail-safe operation through architectural design and Real Time error checking, errors as well as device design development in compliance with the regulations and delivered to a high quality
- Managing suppliers in detailed software design, coding and documentation with consideration of medical device classification
- Applying security protocols for wireless communication as well as planning and reviewing the verification and validation of the software to ensure safe and secure operation
- Generating Design Controls documentation, authoring and reviewing documents and ensuring the quality and compliance to applicable regulations
START: 10/2018
DURATION: 6MM+
LOCATION: Basel, Switzerland
REF.NR.: BH13220
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:
- 8+ years' experience in software development with main focus on medical devices for parenteral administration and generating DHF documentation, including designing input requirements, technical specifications, design verification, validation, and transfer.
- Excellent technical writing skills, ideally in Design Controls
- Good understanding of medical device regulations, such as FDA 21CFR 820 and EU Medical Device Directive coupled with combination products (US) and standards
- General understanding of Pharmaceutical Development, Human Factors Engineering and Risk management
- Good organisation and communication skills
- Languages: fluent English both written and spoken
YOUR TASKS:
- Specifying requirements of software components and defining architecture for future platforms
- Collaborating with human factors engineers and electronics experts to ensure appropriate hardware defined for software requirements
- Ensuring data security and integrity as well as fail-safe operation through architectural design and Real Time error checking, errors as well as device design development in compliance with the regulations and delivered to a high quality
- Managing suppliers in detailed software design, coding and documentation with consideration of medical device classification
- Applying security protocols for wireless communication as well as planning and reviewing the verification and validation of the software to ensure safe and secure operation
- Generating Design Controls documentation, authoring and reviewing documents and ensuring the quality and compliance to applicable regulations
START: 10/2018
DURATION: 6MM+
LOCATION: Basel, Switzerland
REF.NR.: BH13220
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
-
Kategorie:
Medien/Design, Ingenieurwesen/Technik