Senior Regulatory Affairs Lead — AI Medical Devices

🔎 Title: Senior Regulatory Affairs Consultant🔸 The CompanyIf you are a QA/RA professional with an interest in innovation and groundbreaking development, we have an incredible role for you. This is a chance to join an established midsize Software as a Medical Device company.🔹 As a Regulatory Affairs Consultant your mission is to:Develop and execute...

A fast-growing femtech startup in Paris is seeking a Regulatory Affairs Specialist to oversee regulatory and quality activities. You will execute regulatory activities for medical devices, own critical parts of the Quality Management System, and ensure compliance in a fast-paced environment. The ideal candidate has a degree in Engineering or Regulatory...

Senior Regulatory Affairs Program Manager (Koren speaking) Sonio is a mission-driven company focused on improving women’s and children’s health through AI‑driven prenatal screening tools. We are seeking a senior professional to lead regulatory affairs for our AI/ML‑enabled medical devices. About The RoleYou will join a newly created team working on...

A leading MedTech recruitment firm is seeking a Senior Regulatory Affairs Consultant to develop and execute regulatory strategies that align with global requirements. The role requires 5-7 years of regulatory experience within medical devices, expertise in leading FDA submissions, and a solid grasp of project management. This position offers the opportunity...

A medical imaging company in Paris is seeking a Clinical Affairs Manager to lead initiatives on clinical performance testing and validation. This position demands expertise in radiological devices and collaboration with cross-functional teams to ensure compliance with regulatory standards. The ideal candidate has a background in clinical evaluation and...

Prise de poste non définie BAC +5 Paris Nombre de postes non défini CDI Rémunération non définie **Description du poste et des missions**: **WHO WE ARE** Cellectis is a **global clinical-stage biopharmaceutical** company. **Pioneers and innovators** in our field, our mission is to develop **innovative treatments** for **patients with unmet medical...

Company DescriptionTheraPanacea is a European scale up in AI-driven precision oncology, headquartered in Paris. Built on world-class research from CentraleSupélec, Inria, and Gustave Roussy, we develop advanced medical AI platforms that elevate cancer care through automation, personalization, and clinical precision. Our flagship platform, ART-Plan, is...

This role is for one of the Weekday's clientsMin Experience: 8 yearsLocation: EuropeJobType: full-timeWe are seeking an experienced Veeva Regulatory Information Management (RIM) professional with strong expertise in Ennov to lead and support global regulatory operations and system implementations. The ideal candidate will play a critical role in managing...

**About the Job** Join Excelya, where Audacity, Care, and Energy define who we are and how we work. We believe in creating bold solutions and fostering an inclusive environment where collaboration and individual growth go hand in hand. This role is an exciting opportunity to contribute to a dynamic, ambitious team. You will play a critical part in driving...

A global leader in micro-connectors is seeking a Head of Regulatory Affairs & Quality in Paris. You will build and lead a team focused on compliance with ISO 13485 and QSR standards, while overseeing multi-site operations. The ideal candidate has over 10 years of experience in the medical device industry, strong project management skills, and fluency in...