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Product Development Engineer
Eingestellt von Harvey Nash IT Recruitment Switzerland
Gesuchte Skills: Engineer, Design
Projektbeschreibung
Role: Product Development Engineer
Place of work: Oberdorf, Baselland
Project start date: 16.01.2017
Project end date: 30.06.2017
Workload/weekly working hours: 100%/40 hours
Product Development/Quality Engineer
Overall Responsibilities:
*Remediation of existing Risk Management documentation (Design & Clinical Risk Management, Risk Management Report, and Risk Management Plan) to the Product Risk Management Process.
Functional Experience Requirements
. Three or more years experience with prior experience in the design and development of medical devices or pharmaceuticals preferred.
. Strong background in Product Risk Management with experience in creation, review, and approval of risk management documentation (DFMEAs and PFMEAs).
. Strong analytical skills.
Additional Requirements and Competencies:
Information exchange and collaboration between internal, local, external and foreign partners is essential. Close cooperation with internal departments, domestic and international authorities as well as the conscientious preparation of the required documents ensures compliance with Medical Device Regulations (EU MDD, US FDA, JP PAL).
Proficiency in Microsoft Office (Excel, Word, etc.) and the ability to effectively manage multiple priorities and tasks.
Place of work: Oberdorf, Baselland
Project start date: 16.01.2017
Project end date: 30.06.2017
Workload/weekly working hours: 100%/40 hours
Product Development/Quality Engineer
Overall Responsibilities:
*Remediation of existing Risk Management documentation (Design & Clinical Risk Management, Risk Management Report, and Risk Management Plan) to the Product Risk Management Process.
Functional Experience Requirements
. Three or more years experience with prior experience in the design and development of medical devices or pharmaceuticals preferred.
. Strong background in Product Risk Management with experience in creation, review, and approval of risk management documentation (DFMEAs and PFMEAs).
. Strong analytical skills.
Additional Requirements and Competencies:
Information exchange and collaboration between internal, local, external and foreign partners is essential. Close cooperation with internal departments, domestic and international authorities as well as the conscientious preparation of the required documents ensures compliance with Medical Device Regulations (EU MDD, US FDA, JP PAL).
Proficiency in Microsoft Office (Excel, Word, etc.) and the ability to effectively manage multiple priorities and tasks.
Projektdetails
Geforderte Qualifikationen
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Kategorie:
Medien/Design, Ingenieurwesen/Technik