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
Hybrid Regulatory Affairs Manager, CMC for mRNA Vaccines in North East employer: GlaxoSmithKline plc
GSK is an exceptional employer that fosters a culture of innovation and collaboration, making it an ideal place for professionals seeking to make a meaningful impact in the biopharma industry. With a commitment to employee growth through continuous learning opportunities and a flexible hybrid working model, GSK empowers its workforce to thrive while contributing to groundbreaking advancements in healthcare. Located in vibrant London, employees benefit from a dynamic work environment that prioritises ambition for patients and accountability for results.
