Regulatory Affairs Specialist
- Arbeidsgiver
- Laerdal Medical AS
- Stillingstittel
- Regulatory Affairs Specialist
- Frist
- 15.02.2019
- Ansettelsesform
- Fast
The Company
Laerdal Medical is an international market leader in training and therapy solutions for emergency medicine and critical care. Our products and services are used by hospitals, ambulance services, first aid organizations, educational institutions and others, around the world. We are a dynamic and energetic organization consisting of people from a wide variety of cultures and backgrounds. By 2020, we have a goal of helping save 500,000 more lives. Every year.
What you will do
As a Regulatory Affairs Specialist, you will be part of the Corporate Quality and Regulatory department, located in Stavanger. In your role you will develop strategies and plans to ensure product approvals of new and existing electronic products and software applications. Furthermore, you will:
•Provide regulatory support on compliance with applicable product regulations;
•Issue EU Declaration of Conformity for CE marked products;
•Manage relationship with 3rd parties in product approval activities;
•Provide internal training related to regulatory compliance;
•Perform internal audits of the Laerdal Quality System.
About you
You have a University degree in natural science, engineering or in law and 2-3 years relevant experience.
•Experience from product development and/or product approval of electronic products;
•Fluent in English and with excellent written and oral communication skills;
•Able to work independently and to be proactive;
•Well organized with attention to details.
About your colleagues
You will work in a diverse multi-cultural and international environment with people who strive to help save lives. We value each other’s professionalism and enthusiasm and enjoy solving complex challenges together.
Accepting the challenge
For more information about the position contact Mari Kaada, mari.kaada@laerdal.com,
or phone +47 51511630.
Send your application and CV marked “Regulatory Affairs Specialist” to HR@laerdal.no. Application deadline is 15 February 2019.
Om arbeidsgiveren
Laerdal Medical is an international market leader in training and therapy products for emergency medicine and critical care. Our products and services are used by hospitals, ambulance services, simulation centers, educational institutions and others around the world. We are a dynamic and energetic organization consisting of people from a wide variety of cultures and backgrounds. By 2020, we have a goal of helping save 500,000 more lives. Every year.
- Sektor
- Privat
- Sted
- TANKE SVILANDS GATE 30, 4007 Stavanger
- Bransje
- Industri og produksjon
- Stillingsfunksjon
- Annet
Spørsmål om stillingen
- Kontaktperson
- Mari Kaada
- Stillingstittel
- Corporate Regulatory Affairs Manager
- Telefon
- 51 51 16 30
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TANKE SVILANDS GATE 30, 4007 Stavanger