R&D Quality Lead — Medical Devices & Comb. Products
Listed on 2026-10-17
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Quality Assurance - QA/QC
Regulatory Compliance Specialist
Sandoz UK & Ireland is seeking a Quality Manager to lead complex projects and ensure cGMP compliance in Drug Delivery Device Development. You will manage the Design History File portfolio and drive quality across development programs, ensuring alignment with Medical Device and Combination Product regulations.
You’ll collaborate across functions, lead inspections and audits, and support deviation and change control processes while upholding Sandoz standards and a commitment to patient safety.
Our team is growing, and we are hiring a R&D Quality Lead — Medical Devices & Comb. Products in Cambridge, England, United Kingdom.
Take a moment to read everything above and see whether this role is right for you.
This posting is for the R&D Quality Lead — Medical Devices & Comb. Products role at Sandoz UK & Ireland, based in Cambridge, England, United Kingdom.
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