GSK hires a Regulatory Affairs Manager for CMC in mRNA vaccine development. You will steer regulatory strategies, collaborate with regulatory, manufacturing, quality, and development teams, and ensure timely approvals across US/EU regions.
You will manage CMC documentation for submissions and guide cross-functional workstreams to deliver high-quality dossiers. You should have a life sciences degree with 2+ years in CMC regulatory affairs, plus experience with US/EU submissions and strong
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Hybrid Regulatory Affairs Manager, CMC for mRNA Vaccines in North East employer: GSK
GSK is an exceptional employer, offering a dynamic work culture that fosters collaboration and innovation in the heart of Stevenage. With a strong commitment to employee growth, you will have access to extensive development opportunities while working on groundbreaking medicine projects. The hybrid work model and future relocation to Cambridge provide a unique advantage, ensuring a vibrant environment for both personal and professional advancement.
