Regulatory Affairs Specialist

About Our ClientInternational healthcare organization active in the medical device sector, supporting patient care through innovative products distributed across multiple global markets.Job DescriptionAs a successful Regulatory Affairs Specialist - Medical Devices - EN, you will have the following responsibilities:Coordinate product registrations across...

Jobat is seeking a Regulatory Affairs Specialist for an international healthcare organization active in the medical device sector. You will coordinate registrations across international markets and prepare regulatory documentation with internal and external stakeholders.You will support ongoing compliance activities, manage regulatory aspects of changes,...

Michael Page is seeking a Regulatory Affairs Specialist for Medical Devices (EN) to coordinate international registrations, prepare regulatory submissions, and maintain lifecycle compliance. The role involves liaising with manufacturers, distributors, and authorities, and ensuring alignment with MDR requirements.The successful candidate will have 1–3 years...

GC Corporation was founded in 1921 in Japan and has developed itself into one of the most prominent companies in the development, production and distribution of a very wide range of dental products. Since 1972 GC Europe NV, our European Headquarter is located at the Researchpark Haasrode in Leuven (Belgium). GC Europe NV supports and leads our different...

GC Europe NV is seeking a Scientific Affairs Specialist for the EMEA region. The role focuses on creating and communicating scientific information to support sales, product claims, and regulatory submissions, in collaboration with internal teams and external academics.The position requires a Master’s degree (PhD/DDS preferred), English fluency, strong...

Intro At Vaigo, we help organisations navigate the complex world of employee mobility. Our platform simplifies mobility policy management, promotes sustainability, and empowers employees with the tools they need to move smarter. We're an AI-first company: every hire is expected to use AI to multiply their own output, not just speed it up — we're building...

Om de groei van onze wereldwijde activiteiten te ondersteunen, zijn we op zoek naar een Arts – specialist in Cardiologie die ons Core Labs-team in Leuven komt versterken. In deze voltijdse kantoorfunctie werk je samen met een team van artsen en andere experten aan de beoordeling van cardiale onderzoeken binnen internationale klinische studies. Je levert...

Our Site Contracts Team is currently seeking a full-time, Contract Specialist to join our Sites Contracts Team in Leuven. This position plays a key role in the study start-up and clinical trial management processes at Medpace. As a Site Contract Specialist, you will have full responsibility for the life cycle of each contract through the preparation,...

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