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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

Recovery and Purification Supporter

Kalundborg

Are you someone who excels in a dynamic and fast-paced setting where teamwork is essential for success?

Indrykket:

Associate Research Scientist - In Vivo pharmacology

Måløv

Are you passionate about in vivo liver disease research, performing decision making pharmacology studies, digital transformation and being involved in drug discovery?

Indrykket:

Scientist - Mammalian Cell Cultivation

Bagsværd

Do you have experience with mammalian cell cultivation at a pilot scale or motivated to learn?

Indrykket:

Senior Analytical Technician

Ballerup

Are you our experienced analytical technician in the small molecule Pharmaceutical Development?

Indrykket:

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