Dieses Jobangebot ist archiviert und steht nicht mehr zur Verfügung.
Vakante Jobangebote finden Sie unter Projekte.
Vakante Jobangebote finden Sie unter Projekte.
Product Development Engineer
Eingestellt von Randstad (Schweiz) AG
Gesuchte Skills: Engineer, Design, Engineering
Projektbeschreibung
Product Development Engineer
We are pleased to present this opportunity to you on behalf of our client. They are one of the world's most reputable Pharmaceutical Institutions.
In this position you will:
be responsible for the maintenance of existing implants and instruments.
be responsible for the maintenance of existing Technical File and Design History File documentation.
able to understand and comprehend existing techfile documentation in English
write Standard Evaluation EN ISO 14630:2012 and EN ISO 14602:2011
write Design and Clinical Risk Management
Additional Tasks
Information exchange and collaboration between internal, local, external and foreign partners
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).
Your Profile
For this position we are looking for a team player with strong initiative.
You will have earned a higher degree in engineering and would preferably have some practical experience in a regulated industry.
You are self-motivated and take responsibility in your projects.
You are a creative problem-solver with excellent communication skills and strong leadership ability.
You should have a keen interest in the interrelations between medicine and technology and a strong desire to work in a global company.
Ability to communicate in both spoken and written English is required. Communication skills in German are highly preferred.
With this opportunity, you will have a great opportunity to work in a global and will have good exposure in the business.
We are pleased to present this opportunity to you on behalf of our client. They are one of the world's most reputable Pharmaceutical Institutions.
In this position you will:
be responsible for the maintenance of existing implants and instruments.
be responsible for the maintenance of existing Technical File and Design History File documentation.
able to understand and comprehend existing techfile documentation in English
write Standard Evaluation EN ISO 14630:2012 and EN ISO 14602:2011
write Design and Clinical Risk Management
Additional Tasks
Information exchange and collaboration between internal, local, external and foreign partners
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).
Your Profile
For this position we are looking for a team player with strong initiative.
You will have earned a higher degree in engineering and would preferably have some practical experience in a regulated industry.
You are self-motivated and take responsibility in your projects.
You are a creative problem-solver with excellent communication skills and strong leadership ability.
You should have a keen interest in the interrelations between medicine and technology and a strong desire to work in a global company.
Ability to communicate in both spoken and written English is required. Communication skills in German are highly preferred.
With this opportunity, you will have a great opportunity to work in a global and will have good exposure in the business.
Projektdetails
Geforderte Qualifikationen
-
Kategorie:
Medien/Design, Ingenieurwesen/Technik