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EU Regulation 2017/745 Jobs in Stockholm

2 open positions · Updated 1 month ago

2 roles Mid 2 3–5 yrs experience Stockholm Full-time newest 1 month ago

Also hiring: ISO 13485 Azure DevOps FDA 21 CFR Part 820 ISO 14971 Medical Devices Post-Market Surveillance

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Regulatory Affairs Engineer, Manufacturing Lifecycle Hybrid

Join Neko Health as a Regulatory Affairs Engineer to ensure compliance in manufacturing and distribution of medical devices.

Neko Health Stockholm Published 1 month ago

FDA 21 CFR Part 820 EU Regulation 2017/745 Visual Studio Code Azure DevOps ISO 13485

Regulatory Affairs Engineer, Post-Market Surveillance

Join Neko Health as a Regulatory Affairs Engineer to enhance post-market surveillance processes for medical devices.

Neko Health Stockholm Published 1 month ago

EU Regulation 2017/745 Post-Market Surveillance Regulatory Affairs ISO 14971 Medical Devices

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