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CMC Regulatory Project Manager

Job reference:267679

Location:Various (global)

Category:Latest jobs

Closing date:

Start date:

Contact:

GlaxoSmithKline


Are you looking for a role where you can be responsible for the CMC regulatory activities of multiple projects and dosage forms?  If so, this could be an ideal opportunity for you to explore.

As a Regulatory Affairs Project Manager,  you will represent Global CMC Regulatory on Regulatory Networks and Matrix Teams providing regulatory advice and guidance to Preclinical Development (PCD), Biopharm, Global Manufacturing and Supply (GMS), Clinical Supplies, Commercial, Quality Assurance, 3rd Party Contract Management and Office of the Chief Medical Officer (OCMO) to produce appropriate CMC components for global regulatory dossiers with appropriate guidance from supervisor, as necessary.


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