Exeltis is a pharmaceutical company seeking a Regulatory Affairs Associate to support regulatory development and lifecycle management of pharmaceutical products in Madrid on-site. You will prepare eCTD modules, manage submissions and renewals, archive documents, and collaborate with Clinical Operations in the US as needed.
3+ years of regulated industry experience and fluent English are required. Join a dynamic team and help ensure timely regulatory filings while staying up-to-date with ICH,
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📌 Regulatory Affairs Associate - Temporary, Madrid (On-Site)
🏢 Exeltis
📍 Madrid
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