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NemeraLyon, France. Full-time.

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Regulatory affairsPharmaceutical industryManufacturingCustom developmentContract manufacturingMedical devicesGlobal medical device regulationsRegulatory documentationContinuous improvementDocument management systemEnrollment in a Bachelor's or Master's ProgramAttention to detailWillingness to learnOrganizational and analytical skillsTalent Acquisition

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