10 ott - Verona
Parexel
Parexel in Italy (Catania area) is seeking a Senior Regulatory Affairs Associate to drive post-approval regulatory activities focused on CMC for biologics and vaccines. You will collaborate across manufacturing, QA, QC, and regulatory teams to shape submission strategies and ensure worldwide compliance.
Responsibilities include developing post-approval CMC submission strategies, assessing regulatory impact of quality changes, coordinating submissions, and writing or reviewing content for health
J-18808-Ljbffr
11 ott - Roma
Experteer Italy
11 ott - Bologna
Hays
11 ott - Caronno Pertusella
Foürme
11 ott - Sant'Apollinare
Adecco