Device Risk Lead — ISO 14971 & Regulatory Excellence
Listed on 2026-10-18
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Engineering
Regulatory Compliance Specialist, Medical Device Industry, Biomedical Engineer, Quality Engineering
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
This role, Device Risk Lead — ISO 14971 & Regulatory Excellence at GSK, could be your next career step.
Are you ready to take on the Device Risk Lead — ISO 14971 & Regulatory Excellence role at GSK?
We would love to welcome a new Device Risk Lead — ISO 14971 & Regulatory Excellence to our organisation in Ware, England, United Kingdom.
For the Device Risk Lead — ISO 14971 & Regulatory Excellence position at GSK, we are reviewing applications now.
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