BioTalent is partnering with a SME Class 2 Device business in Reading to recruit a Regulatory Affairs professional. The role offers exposure to both new product development and introductions, with guidance from an experienced leader and a broad range of tasks.
The successful candidate will have at least 3 years in regulatory affairs for Medical Devices or IVD, hands-on ISO 13485 experience, and familiarity with MDR updates, technical files, and registrations.
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Regulatory Specialist – Medical Devices (NPD & MDR, Global) in Reading employer: BioTalent
Join a dynamic and innovative biosimilars organisation in London, where your expertise as a Manager of Analytical Development will be valued and impactful. We foster a collaborative work culture that prioritises employee growth through continuous learning and development opportunities, ensuring you can advance your career while contributing to cutting-edge scientific advancements. With a focus on biosimilarity assessment and analytical strategy, you'll play a crucial role in shaping our scientific capabilities in a supportive environment that champions teamwork and excellence.
