Job TitleRegulatory Affairs Specialist Job Description Your role: Develop global regulatory strategies for software medical devices ensuring ongoing compliance throughout the product lifecycle. Prepare and manage regulatory submissions and approvals in the US, Europe, and Canada. Represent Regulatory Affairs on
Job TitleSenior Risk Manager Azurion Eye - AI, cloud, Sa(N)MD Job Description Senior Risk Manager Azurion Eye - AI, cloud, Sa(N)MD As Senior Risk Manager within the Azurion Eye program, you own and continuously evolve the
Job Description We are looking for a motivated student! Do you want to know what its like to be part of one of the largest multinational companies in the pharmaceutical industry? We offer an internship opportunity
Job TitleSenior Software Design Quality Engineer - AI Job Description In this role, you have the opportunity to As a highly experienced Senior Design Quality AI Engineer you will have opportunity to lead design assurance activities
Job TitleClinical Development Scientist Job Description Job Responsibilities Owns and drives end‑to‑end clinical evidence strategy, defining and linking clinical need, value, TPP, claims, endpoints, and evidence to regulatory acceptance and post‑market requirements with full lifecycle traceability (AD
Job TitleSenior Clinical Development Scientist (Medical Imaging / CT) Job Description As a Clinical Development Scientist, you will help shape the clinical evidence behind Philips’ next-generation CT innovations, including Photon Counting CT. In this highly visible
Job TitleClinical Evaluation & Compliance Leader, Enterprise Informatics Job Description The Clinical Evaluation and Compliance Leader leads the clinical evaluation, post-market clinical follow-up, and evidence compliance strategy for the Enterprise Informatics portfolio. The role ensures that
Barrington James is partnering with a growing pharmaceutical consultancy in the Netherlands to recruit an experienced Regulatory Affairs professional. Als u meer wilt weten over de vereisten voor deze functie, lees dan verder voor alle relevante informatie.
Usono in Eindhoven is seeking a proactive Quality Assurance & Regulatory Affairs Engineer to support EU MDR compliance, technical documentation, and lifecycle management of our medical device portfolio. Zorg ervoor dat u solliciteert met alle gevraagde informatie,
Turn a CE-marked breakthrough into a manufacturing line. Alle aanvullende informatie die u voor deze baan nodig heeft, vindt u in de onderstaande tekst. Zorg ervoor dat u deze grondig leest en vervolgens solliciteert. Xeltis builds
Job Description Wacht niet met solliciteren na het lezen van deze omschrijving; er wordt een groot aantal sollicitaties voor deze vacature verwacht. As a Senior Clinical Operations Consultant, you will play a key leadership role in
Turn a CE-marked breakthrough into a manufacturing line. Xeltis builds regenerative cardiovascular devices: implants engineered to be gradually restored by the patient’s own living tissue. In April 2026 our lead device, aXess, reached CE mark. We