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Orifarm

Specialist, Regulatory Affairs (Temporary Position)

Odense S and Søborg

As Regulatory Affairs Specialist, you will be responsible for lifecycle management of products manufactured at Orifarm’s own manufacturing sites. Therefore, you will collaborate closely with colleagues across functions, such as chemists, formulation specialists and co-workers within Quality, Supply Chain, Manufacturing and Sales.

Further, your main responsibilities include to:

  • Gather information and documentation for variation applications
  • Update dossier sections
Orifarm

Postdoc on the DANIDA-funded “Cities of Youth” project on migration and health in Uganda

Odense M

The Danish Centre for Health Economics (DaCHE) and Danish Institute for Advanced Study (DIAS), University of Southern Denmark, seeks to...

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