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:
- Ideally 8+ years' of experience in device development of parenteral delivery systems
- Advanced technical writing skills eg with use of Design Controls
- Know-how of medical device regulations such as FDA 21CFR 820, EU Medical Device Directive and of combination products
- Familiarity with product design, design for manufacturing as well as technical knowledge of primary containers development and autoinjector development
- Experience in generating DHF documentation, including design input requirements, technical specifications, design verification, design transfer and design validation would be an asset
- Languages: fluent English both written and spoken
YOUR TASKS:
- Leading technical development activities for medical devices such as Autoinjector, Safety syringes
- Working with third party suppliers and specifying requirements of device components to guarantee that components are delivered and controlled to the required quality for clinical trials as well as commercial production
- Reporting technical aspects related to the device development project to the device project leader as well as coordinating technical activities responsible for packaging, human factors engineering, verification testing and risk management
- Contributing to a high-quality Design History File for parenteral delivery injection systems by ensuring quality and compliance to applicable regulations
- Ensuring device design development in compliance with the regulations and in a high quality as well as analysing of out-of-specification product and developing solutions to prevent re-occurrence
- Supporting to prepare medical device registration documents and answering health authority questions
START: ASAP
DURATION: 06MM+
LOCATION: Basel, Switzerland
REF.NR.: BH12414
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:
- Ideally 8+ years' of experience in device development of parenteral delivery systems
- Advanced technical writing skills eg with use of Design Controls
- Know-how of medical device regulations such as FDA 21CFR 820, EU Medical Device Directive and of combination products
- Familiarity with product design, design for manufacturing as well as technical knowledge of primary containers development and autoinjector development
- Experience in generating DHF documentation, including design input requirements, technical specifications, design verification, design transfer and design validation would be an asset
- Languages: fluent English both written and spoken
YOUR TASKS:
- Leading technical development activities for medical devices such as Autoinjector, Safety syringes
- Working with third party suppliers and specifying requirements of device components to guarantee that components are delivered and controlled to the required quality for clinical trials as well as commercial production
- Reporting technical aspects related to the device development project to the device project leader as well as coordinating technical activities responsible for packaging, human factors engineering, verification testing and risk management
- Contributing to a high-quality Design History File for parenteral delivery injection systems by ensuring quality and compliance to applicable regulations
- Ensuring device design development in compliance with the regulations and in a high quality as well as analysing of out-of-specification product and developing solutions to prevent re-occurrence
- Supporting to prepare medical device registration documents and answering health authority questions
START: ASAP
DURATION: 06MM+
LOCATION: Basel, Switzerland
REF.NR.: BH12414
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