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Zealand Pharma A/S

Regulatory Affairs Clinical Specialist

Søborg

Due to many activities in our exciting clinical development projects, we are seeking two new colleagues to our Regulatory Affairs function.

Your key responsibilities will be to contribute with regulatory expertise to global strategies and execution within your assigned project(s). You will be the regulatory responsible in the clinical trial teams and provide regulatory guidance and support for the planning, execution, and reporting of clinical trials worldwide.

Zealand Pharma A/S

Quality Supporter

Hillerød

Are you THE facilitator of problem solving on a professional level, and THE driver of the handling of deviations, from initial discovery to...

Indrykket:
Viio Technologies APS
Gem

Quality Assurance Engineer

København

We seek a highly skilled Quality Assurance Engineer to join our team.

Indrykket:
Hentet fra The Hub

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