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Regulatory Affairs Manager
Medical Devices
This is an opportunity to work in a key role with a broad spectrum of responsibilities in a listed medical device company and to contribute to the growth of the company.

The company is active in a field, highly contributing to save patients lives world wide.
Your responsibilities will be among other listed below.

• Creating and submitting product registrations worldwide. New product submissions.
• Country registrations worldwide.
• Project planning and coordination of regulatory submissions.
• Take part in the creation and in continuous improvements of electronic documentation system with regard to regulatory documentation.
• Surveillance of new and changed Regulatory requirements worldwide, and to communicate such changes to relevant staff.
• Take part in clinical evaluation projects as responsible RA.
• Take part in project development /improvement projects as responsible RA.
• Take part in global production development as responsible RA.
• Approval of marketing material as responsible RA.

Success factors
As a person you are humble, responsible, independent and committed to your work. You are thorough and structured in your work and have very good cooperation and communication skills.

Please contact Erik Düring for more information.
Rekryteringsspecialisten AB
Mobil 0708-999 469