Mira is seeking a Regulatory Submission Specialist to lead and support the preparation, review and submission of regulatory documentation for in vitro diagnostic devices. You will ensure clinical, analytical, usability, risk-management, quality, and labelling evidence is compiled into submission-ready documentation, supporting regulatory compliance throughout the product lifecycle.
The ideal candidate has experience in regulatory submissions, technical documentation and international IVD
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Remote Regulatory Submissions Specialist – EU IVDR/CE employer: Mira
Mira is an exceptional employer that fosters a dynamic and collaborative work culture, perfect for those looking to make a significant impact in the B2B sector. With a strong emphasis on employee growth, you will have access to continuous learning opportunities and the chance to shape our sales processes while working remotely. Join us to be part of a forward-thinking team that values innovation and rewards your contributions to our revenue engine.
