IVDR Regulatory Affairs Specialist – IVD Compliance

il y a 1 jour


Lyon, France Astek Temps plein

A leading CRO solutions provider is recruiting a Senior Preclinical Biostatistician in Lyon, France. The role focuses on ensuring compliance with evolving IVDR regulations. Candidates should have a higher education in Life Sciences and 2-5 years of experience in regulatory affairs for medical devices or IVDs. Key responsibilities include preparing technical documentation and supporting CE marking activities, while collaborating with cross-functional teams. This is a great opportunity to contribute to crucial regulatory processes.
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