10 ott - Firenze
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.
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You will collaborate across manufacturing, QA, QC, and regulatory teams to shape submission strategies and ensure worldwide compliance. xbvzest
Responsibilities include developing post-approval CMC submission strategies, assessing regulatory impact of quality changes, coordinating submissions, and writing or reviewing content for health
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