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This list contains only the countries for which job offers have been published in the selected language (e.g., in the French version, only job offers written in French are displayed, and in the English version, only those in English).
Lead software tool validation at Neko Health in Stockholm. Requires 10+ years in CSV within regulated medtech, GAMP 5 and FDA CSA expertise, and a pragmatic, risk-based approach to AI-enabled systems.
Regulatory Affairs Engineer role in Stockholm focusing on design transfer, GMP compliance and FDA shipment documentation. Join Neko to own manufacturing regulatory processes end to end and help scale preventative care technology.
Join Neko in Stockholm as a Regulatory Affairs Engineer for Post-Market Surveillance. Run PMS processes across the device portfolio, produce trend reports, and support Notified Body documentation in a cross-programme role.