Responsible for the investigation, coordination, and resolution of assigned tasks related to Health Hazard Evaluations, Quality Holds, and Field Actions
Support functional areas to resolve product and process issues
Strong knowledge of medical device requirements
Strong knowledge of compliance with the applicable international regulatory requirements (ie, FDA QSRs, ISO 13485, MEDDEV)
Ensure an efficient and compliant PMS processes
Post Market Surveillance Engineer (f/m)
Bachelor's degree in natural sciences, engineering or similar
3-5 years of experience within a Medical Device industry with a Quality/ Regulatory Affairs background
Knowledge of PMS is of advantage
Fluent in English and German
Good communication and writing skills
Permanent position in an international company
Possibility to start as soon as possible or on agreement
Flexible working hours and a team-oriented environment
The opportunity to develop your international experience and improve your carrer
Are you interested in this position, or a similar role? Then I am eager to receive your application and discuss the position with you!
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Your contact Frau Natasa Emmisberger, Teamleader Delivery & Sourcing, looks forward to answering your questions by phone +41 58 233 4513 or eMail.
You can apply directly online, or by eMail. Please mention reference JN -112017-47534 in your application.