GSK is seeking a Device Risk Management Lead to establish and continuously improve risk management for medical devices and drug–device combinations across PDDS, aligned with ISO 14971 and global regulations. The role requires leading RMF, conducting risk assessments and guiding risk controls throughout product lifecycle.
You will collaborate across Human Factors, Device Engineering, Formulation, Regulatory and Quality, driving risk thinking, evidence packs for inspections, and cross-functional
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Device Risk Lead — ISO 14971 & Regulatory Excellence in Ware 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.
