04 ott - Italia
Parexel International
Parexel International is seeking a Regulatory Affairs Consultant to lead post-approval activities focused on CMC for vaccines or biologics. The role allows office or home-based work across Europe.
You will develop submission strategies, assess change controls, coordinate cross-department submissions, and manage information management systems. Fluent English required; remote options available.
J-18808-Ljbffr
10 ott - Spilimbergo
BiDoc
10 ott - Bronte
Work & Progress
10 ott - Emilia-Romagna
Archimede
10 ott - Torino
Jet HR