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An ideal role for someone experienced within QA/QC roles working to ISO17025
Providing support within the regulatory function maintaining and expanding the specified product registrations within UK and EU.
This role is vital to the UK operations of this client, as a standalone Quality role. The main focus areas of this role are QMS/eQMS and RP/RPi duties.
You will utilise specialist knowledge relating to cell culture techniques and GMP standards to support with developing manufacturing processes for novel clinical trials in the CGT space
We are seeking a meticulous and dedicated Senior Regulatory Affairs Associate with a strong background in Regulatory Affairs (Medical Devices). The successful candidate will be responsible for ensuring compliance with regulatory standards (MDD-MDR experience is essential).
This is an exciting opportunity to join an early-stage biotechnology startup as a Research Associate where your drive and expertise will spearhead the refinement of their TCR engineering processes. You'll play a crucial role in curating datasets to inform their AI algorithms, affirming their platform's efficacy, and identifying TCRs.
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