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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:
- At least 8 years of experience in device development of parenteral delivery systems, eg, drug/device combination products with main focus on medical devices for parenteral administration
- Excellent technical writing skills (eg, Design Controls)
- Solid understanding of medical device regulations (FDA 21CFR 820, EU Medical Device Directive) paired with competency of Product Design and Design for Manufacturing
- Good technical knowledge of primary containers development and autoinjector development
- General understanding of Human Factors Engineering, Risk management, clinical trial processes and requirements and pharmaceutical development
- Languages: fluent English both written and spoken
YOUR TASKS:
- Running and leading technical development activities for medical devices
- Preparing design controls documentation while contributing to a high-quality Design History File (DHF)
- Reviewing and changing the DHF documents while guaranteeing quality and compliance to applicable regulations of the DHF elements of the assigned projects
- Ensuring device design development in compliance with the regulations and delivered at a high quality
- Consulting the development of medical devices and combination products
START: ASAP
DURATION: 06MM+
LOCATION: Basel, Switzerland
REF.NR.: BH10919
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
YOUR EXPERIENCE/SKILLS:
- At least 8 years of experience in device development of parenteral delivery systems, eg, drug/device combination products with main focus on medical devices for parenteral administration
- Excellent technical writing skills (eg, Design Controls)
- Solid understanding of medical device regulations (FDA 21CFR 820, EU Medical Device Directive) paired with competency of Product Design and Design for Manufacturing
- Good technical knowledge of primary containers development and autoinjector development
- General understanding of Human Factors Engineering, Risk management, clinical trial processes and requirements and pharmaceutical development
- Languages: fluent English both written and spoken
YOUR TASKS:
- Running and leading technical development activities for medical devices
- Preparing design controls documentation while contributing to a high-quality Design History File (DHF)
- Reviewing and changing the DHF documents while guaranteeing quality and compliance to applicable regulations of the DHF elements of the assigned projects
- Ensuring device design development in compliance with the regulations and delivered at a high quality
- Consulting the development of medical devices and combination products
START: ASAP
DURATION: 06MM+
LOCATION: Basel, Switzerland
REF.NR.: BH10919
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
Projektdetails
Geforderte Qualifikationen
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Kategorie:
Medien/Design, Ingenieurwesen/Technik