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.
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R&D Quality Lead — Medical Devices & Comb. Products in Cambridge employer: Sandoz UK & Ireland
Sandoz UK & Ireland is an exceptional employer that fosters a collaborative and innovative work culture, empowering employees to make a meaningful impact in the pharmaceutical industry. With a strong focus on professional development, you will have access to numerous growth opportunities while working in a dynamic environment that values compliance and strategic thinking. Located in a vibrant region, Sandoz offers unique advantages such as engaging with diverse NHS channels and contributing to the advancement of healthcare solutions.
