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Product Engineer (Pharmaceutical)
Eingestellt von Randstad (Schweiz) AG
Gesuchte Skills: Engineer, Engineering, Design
Projektbeschreibung
Product Development Engineer
Randstad Professionals is actively looking for a Product Engineer to join their pharmaceutical client in the area of Solothurn, Switzerland. The project will start beginning of January 2016, ending end of June 2016
Role description:
-You will have the responsibility for the maintenance of existing implants and instruments, as well as the responsibility for the maintenance of existing Technical File and Design History File documentation.
-You need to be able to understand and comprehend existing techfile documentation in English
-Writing Standard Evaluation EN ISO 14630:2012 and EN ISO 14602:2011
-Writing Design and Clinical Risk Management
-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).
Requirements:
-Team player with strong initiative
-Higher degree in engineering
-Practical experience in a regulated industry
-Creative Problem-solver
-Strong leadership ability
-Communication skills in German are preferred
If you're up for a new project, please don't hesitate to send in your CV!
Good to know you
(see below)
Randstad Professionals is actively looking for a Product Engineer to join their pharmaceutical client in the area of Solothurn, Switzerland. The project will start beginning of January 2016, ending end of June 2016
Role description:
-You will have the responsibility for the maintenance of existing implants and instruments, as well as the responsibility for the maintenance of existing Technical File and Design History File documentation.
-You need to be able to understand and comprehend existing techfile documentation in English
-Writing Standard Evaluation EN ISO 14630:2012 and EN ISO 14602:2011
-Writing Design and Clinical Risk Management
-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).
Requirements:
-Team player with strong initiative
-Higher degree in engineering
-Practical experience in a regulated industry
-Creative Problem-solver
-Strong leadership ability
-Communication skills in German are preferred
If you're up for a new project, please don't hesitate to send in your CV!
Good to know you
(see below)
Projektdetails
Geforderte Qualifikationen
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Kategorie:
Medien/Design, Ingenieurwesen/Technik