16 ott - Verona
Parexel
Parexel is seeking a Senior Regulatory Affairs Associate to drive post-approval CMC activities for biologics and vaccines. You will collaborate with manufacturing, QA, QC and regulatory teams to shape submission strategies and support variations, renewals and market expansions, with remote options across Europe.
Responsibilities include developing post-approval CMC submissions, assessing regulatory impact of changes, coordinating with cross-functional teams, reviewing study reports, and writing/
#J-18808-Ljbffr
24 ott - Teramo
Abbott
24 ott - Tribiano
Adecco (Italy)
24 ott - Tivoli
AIR
24 ott - Vicenza
Ms C Group