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Device Development Project Manager
Eingestellt von RM IT Professional Resources AG
Gesuchte Skills: Engineering, Design
Projektbeschreibung
Device Development Project Manager wanted for our Basel based client in the pharmaceutical sector.
YOUR EXPERIENCE/SKILLS:
- University degree in Science, Engineering, Mechanical Engineering or equivalent
- 8+ years' working experience in leading device development for parenteral delivery systems
- Proficiency in Project Management as well as product design and design for manufacture
- Good understanding of medical device regulations (FDA 21CFR 820, EU Medical Device Directive)
- Familiarity with Human Factors Engineering and Risk management
- Languages: fluent English both written and spoken
YOUR TASKS:
- Planning and leading technical activities
- Managing technical development activities in collaboration with internal stakeholders as well as leading collaboration with external development partners
- Monitoring and supporting technical development and test and verification work
- Ensuring development and implementation of manufacturing processes
- Coordinating and monitoring technical documentation
START: ASAP
DURATION: 6MM+
LOCATION: Basel, Switzerland
REF.NR.: BH11864
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:
- University degree in Science, Engineering, Mechanical Engineering or equivalent
- 8+ years' working experience in leading device development for parenteral delivery systems
- Proficiency in Project Management as well as product design and design for manufacture
- Good understanding of medical device regulations (FDA 21CFR 820, EU Medical Device Directive)
- Familiarity with Human Factors Engineering and Risk management
- Languages: fluent English both written and spoken
YOUR TASKS:
- Planning and leading technical activities
- Managing technical development activities in collaboration with internal stakeholders as well as leading collaboration with external development partners
- Monitoring and supporting technical development and test and verification work
- Ensuring development and implementation of manufacturing processes
- Coordinating and monitoring technical documentation
START: ASAP
DURATION: 6MM+
LOCATION: Basel, Switzerland
REF.NR.: BH11864
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:
Medien/Design, Ingenieurwesen/Technik