Regulatory Affairs Manager - Olten, Solothurn
vor 1 Monat
Job summaryWe are looking for a Regulatory Affairs Manager to support our company in the areas of quality management and regulatory affairs in the medical device industry.
The successful candidate will have at least 2 years of professional experience in Regulatory Affairs for medical devices, knowledge of ISO 13485, ISO 14971, MDR, IVDR and QSR 21 CFR Part 820. He or she will be responsible for managing regulatory requirements and their updates/monitoring. The position is full-time (60%) with partially working from home possible.
Jobbeschreibung
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The successful candidate will have at least 2 years of professional experience in Regulatory Affairs for medical devices, knowledge of ISO 13485, ISO 14971, MDR, IVDR and QSR 21 CFR Part 820. He or she will be responsible for managing regulatory requirements and their updates/monitoring. The position is full-time (60%) with partially working from home possible.
Jobbeschreibung
, consectetur adipiscing elit. Nullam tempor vestibulum ex, eget consequat quam pellentesque vel. Etiam congue sed elit nec elementum. Morbi diam metus, rutrum id eleifend ac, porta in lectus. Sed scelerisque a augue et ornare.
Donec lacinia nisi nec odio ultricies imperdiet.
Morbi a dolor dignissim, tristique enim et, semper lacus. Morbi laoreet sollicitudin justo eget eleifend. Donec felis augue, accumsan in dapibus a, mattis sed ligula.
Vestibulum at aliquet erat. Curabitur rhoncus urna vitae quam suscipit
, at pulvinar turpis lacinia. Mauris magna sem, dignissim finibus fermentum ac, placerat at ex. Pellentesque aliquet, lorem pulvinar mollis ornare, orci turpis fermentum urna, non ullamcorper ligula enim a ante. Duis dolor est, consectetur ut sapien lacinia, tempor condimentum purus.
Zugang zu allen hochrangigen Positionen und den Job Ihrer Träume erhalten.
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