Regulatory Affairs Specialist
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Regulatory Affairs Specialist · Sweden
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About this role
About the Role As a Global Regulatory Specialist, you will join our Quality & Regulatory Affairs team to help ensure our medical devices and mounting systems meet global regulatory requirements. Please note: This is a hybrid role with 1–3 days per week onsite at our Stockholm office in Östermalm, es
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- Naturvetenskap
- Regulatorisk handläggare/Regulatory affairs specialist
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