BioTalent is currently partnered exclusively with an SME Class 2 Device business who are looking to find their latest addition to their regulatory team
The role with give you:
- A chance to work across both NPD and NPI
- Support by a senior leader that BioTalent has had many years of working with
- Variety of tasks
You will need to bring in:
- Minimum of 3 years of experience within regulatory affairs within Medical Devices or IVD
- Experienced working ISO 13485
- Hands on experience with technical file creation, MDR updates and some exposure to registrations
- Ideal candidates will have worked within global markets such as US or MDSAP countries
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Regulatory Specialist 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.
