29 ott - Marche
Parexel
pParexel is seeking a Senior Regulatory Affairs Associate to lead post-approval CMC activities for biologics and vaccines. You will collaborate across manufacturing, QA, QC, and regulatory teams to shape submission strategies and ensure worldwide compliance. /ppThis role offers remote options in several European locations and focuses on variations, renewals, and market expansions, with responsibilities spanning preparation of submissions, risk mitigation, and regulatory risk escalation. /p #J-18808-Ljbffr