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Medical Device Expert - Human Factor
Eingestellt von RM IT Professional Resources AG
Gesuchte Skills: Client, Design
Projektbeschreibung
Medical Device Expert - Human Factor wanted for our Basel based client in the pharmaceutical sector.
YOUR EXPERIENCE/SKILLS:
- Degree in a proper subject along with relevant working experience in the pharmaceutical or medical device industry
- Experience in planning and writing technical documentation with Medical Device Design Control for Medical Devices and product combinations
- Excellent Project Management skills
- Experince in ISO 13485, ISO14971, MDD and QMS for Medical Devices
- Ideally know-how of Auto-Injectors and Safety Devices
- Languages: fluent German and English both written and spoken
YOUR TASKS:
- Writing, reviewing and approving deliverables (eg procedures) and related tools (eg IT) to ensure GMP compliance
- Managing quality problems and technical matters as well as ensuring global standards and policies
- Releasing of Medical Devices for clinical studies and commercial use
- Supporting Medical Device Risk Management to minimize impact on global supplies and patients as well as representing MD Quality in initiatives and cross-divisional projects
- Meeting internal and external guidelines regarding quality and safety (quality manuals, regulatory cGMP guidelines, health authority requirements, SOPs, HSE, etc.)
- Contributing to internal compliance policy and commenting to regulations
START: ASAP
DURATION: 12MM+
LOCATION: Basel, Switzerland
REF.NR.: BH11622
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:
- Degree in a proper subject along with relevant working experience in the pharmaceutical or medical device industry
- Experience in planning and writing technical documentation with Medical Device Design Control for Medical Devices and product combinations
- Excellent Project Management skills
- Experince in ISO 13485, ISO14971, MDD and QMS for Medical Devices
- Ideally know-how of Auto-Injectors and Safety Devices
- Languages: fluent German and English both written and spoken
YOUR TASKS:
- Writing, reviewing and approving deliverables (eg procedures) and related tools (eg IT) to ensure GMP compliance
- Managing quality problems and technical matters as well as ensuring global standards and policies
- Releasing of Medical Devices for clinical studies and commercial use
- Supporting Medical Device Risk Management to minimize impact on global supplies and patients as well as representing MD Quality in initiatives and cross-divisional projects
- Meeting internal and external guidelines regarding quality and safety (quality manuals, regulatory cGMP guidelines, health authority requirements, SOPs, HSE, etc.)
- Contributing to internal compliance policy and commenting to regulations
START: ASAP
DURATION: 12MM+
LOCATION: Basel, Switzerland
REF.NR.: BH11622
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:
IT Entwicklung, Medien/Design