H3About Mira /h3pMira is a San Francisco-based hormonal health company providing integrative care and hormonal testing for over 300,000 customers. In 2023, we were recognized by Inc. 5000 as America's fastest-growing femtech company. /ph3About Mira /h3pMira is a San Francisco-based hormonal health company providing integrative care and hormonal testing for over 300,000 customers. In 2023, we were recognized by Inc. 5000 as America's fastest-growing femtech company. Mira’s breakthrough innovation was creating the market’s only FDA-compliant at-home hormone monitor with quantitative testing technology. From the beginning, our mission has been to make hormone data accessible and meaningful - so women can understand their bodies and make confident health decisions at every stage of life, from cycle health and family planning to hormonal imbalances and the menopause transition. We are committed to improving real health outcomes through personalized insights, cutting-edge technology, and science-backed data—turning hormone information into practical guidance for everyday wellbeing. /ph3About The Position /h3pWe are looking for a Regulatory Submission Specialist to lead and support the preparation, review, and submission of regulatory documentation for in vitro diagnostic devices. The role will ensure that clinical, analytical, usability, risk-management, quality, and labelling evidence is compiled into clear, submission-ready technical documentation and supports regulatory compliance throughout the product lifecycle. The ideal candidate has experience in regulatory submissions, technical documentation and clinical-performance evidence, and international IVD regulatory requirements. If you want to challenge yourself at a high-growth startup and make a difference for women’s health, please join us! /ph3Responsibilities /h3ulliPrepare, compile, and maintain IVD regulatory submission dossiers and associated technical documentation. /liliReview intended-use statements, product claims, instructions for use,



labelling, advertising materials, and product specifications for regulatory alignment. /liliAssess analytical, clinical-performance, usability, stability, software, and risk-management evidence to confirm it supports the device’s intended purpose and claims. /liliCoordinate evidence collection from internal teams, manufacturers, clinical research organisations, laboratories, quality teams, and external regulatory consultants. /liliIdentify evidence gaps and develop regulatory evidence plans, including requirements for analytical studies, clinical performance studies, and lay-user/self-test studies. /liliSupport the preparation and review of clinical-performance documentation, including study protocols, performance evaluation reports, statistical summaries, and reference-method justifications. /liliPrepare responses to regulatory authority questions, requests for information, and audit-related documentation. /liliMaintain regulatory intelligence on applicable IVD regulations, standards, guidance, and market requirements. /liliSupport post-market regulatory activities, including change assessments, vigilance/adverse-event reporting, recalls, corrective actions, and periodic documentation updates. /liliPartner with Quality, RD, Clinical, Product, and Commercial teams to ensure products remain compliant throughout their lifecycle. /li /ulh3Requirements /h3ulliBachelor degree in Regulatory Affairs, Biomedical Science, Medical Laboratory Science, Biotechnology, Engineering, Life Sciences, or a related discipline.



/lili2+ years of experience in regulatory affairs for medical devices or in vitro diagnostic devices, including preparation of technical documentation or regulatory submissions. /liliExperience supporting or preparing CE-marking documentation under the EU IVDR (Regulation (EU) 2017/746), including technical documentation and performance evaluation requirements. /liliWorking knowledge of IVD quality and regulatory frameworks, including ISO 13485, ISO 14971, ISO 20916, and applicable post-market surveillance and vigilance requirements. /liliExperience reviewing or preparing analytical-performance and clinical-performance documentation for IVDs, including sensitivity, specificity, precision, reproducibility, interference, stability, and method-comparison studies. /liliFamiliarity with relevant IVD standards and guidance, including CLSI EP guidelines; experience with self-tests or consumer-use IVDs is highly desirable. /liliExcellent technical writing, document-control, project-management, and stakeholder-coordination skills, with the ability to work independently in a fast-paced startup environment. /li /ulh3Details /h3pThe role is a remote position, with a 40-hour workweek, flexible working hours, and occasional overlap with the US team. /ph3What We Offer /h3ulliJoin one of the fastest-growing femtech companies in the U.S., driven by a strong mission to advance women’s health and expand access to care /liliBe part of a passionate, highly motivated, and international team dedicated to making a real difference in people’s lives /liliThrive in a fast-paced startup environment where your work directly impacts company growth, strategy, and key decisions /liliEnjoy real opportunities for career growth, with the ability to shape, build, and develop teams as we scale /liliWork in a flexible, fully remote environment that supports autonomy, ownership, and independence /liliReceive a competitive salary along with a performance-based premio system tied to OKRs /li /ul #J-18808-Ljbffr

📌 Regulatory submission specialist (eu ivdr / ce-mark)) (Lombardia)
🏢 MIRA
📍 Lombardia