Lead, CMC

Vor 4 Tagen

Bubendorf, Schweiz CARBOGEN AMCIS Vollzeit

A pharmaceutical company in Switzerland is seeking a Regulatory Affairs Specialist to maintain registration documents and assist with the submission of change documentation. Ideal candidates should have a Master’s or Ph.D. in a relevant field, with at least 5 years of experience in regulatory affairs, specifically in CMC development for biologics. Good English communication skills are essential, alongside knowledge of cGMP regulations. Experience in CDMO and multiple task handling is an advantage.
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