Signatur Biosciences in London, UK is seeking a hands-on Regulatory Affairs & Quality Assurance Officer at an early career stage to support ISO 13485 and IVDR compliance for our qPCR‑based diagnostics.
You will work under the Head of RAQA, gain practical experience across audits, documentation, and QMS maintenance, and travel to our Liège laboratory as needed in a fast-paced startup environment.
#J-18808-Ljbffr
RA & QA Associate — IVD Regulation & Quality employer: Signatur Biosciences
At Signatur Biosciences, we pride ourselves on being an innovative startup that is dedicated to making advanced diagnostic tools accessible to patients worldwide. Our collaborative and data-driven work culture fosters genuine ownership and growth opportunities for our employees, particularly in the Senior Biostatistician role, where you will have the chance to shape the statistical discipline from the ground up. With flexible working arrangements in both the UK and Belgium, competitive salaries, and a commitment to diversity and inclusion, we offer a rewarding environment for those looking to make a meaningful impact in the field of precision medicine.
