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.
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📌 Remote Regulatory Affairs Consultant (Firenze)
🏢 Parexel International
📍 Firenze
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