Role: AI Regulatory Product Counsel Location: Amsterdam Reporting to: Group Head of Privacy, Digital & AI Governance Who We Are Youve ordered from Just Eat Takeaway. Youve bought and sold on OLX. Youve paid with PayU. We
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description As part of Thermo Fisher Scientific’s mission to enable our customers to make the world healthier, cleaner and safer, the Manager, Regulatory Affairs – EMEA is responsible for leading regulatory activities
The Integrated Risk Oversight (IRO) department within Integrated Risk provides independent second‑line oversight on quantitative credit risk topics and securitisation‑related regulatory requirements across ING. Operating at the heart of Group Risk, the department ensures consistent interpretation and
About kaiko.ai Kaiko is building a next-generation agentic clinical AI assistant that helps clinicians reason across patient data, guidelines, and diagnostics. Healthcare decisions are rarely made by a single person or from a single data source.
At Perrigo, we are driven by our mission to Makes Lives Better Through Trusted Health and Wellness Solutions, Accessible to All. We are proud to be a Top 10 player in the European Consumer Self-Care market
Regulatory Affairs Consultant – Software as a Medical Device (SaMD) Direct Contract (initially starting with 12-Months) | Hybrid (Netherlands) | Minimum 3 Days per Week Were partnering with a growing Dutch consultancy specialising in Regulatory Affairs, Quality, and
Regulatory Affairs Officer International At Prothya Biosolutions, we are dedicated to developing and supplying life-saving plasma-derived medicines that improve the lives of millions of patients around the world. Our colleagues are passionate, committed, and always willing to
About the Company Prothya is dedicated to ensuring the registration (market authorization) of its medicinal products is obtained and maintained in compliance with regulatory standards. About the Role The purpose of the job is to compile and
Who We Are At JD.com, also known as JINGDONG, we are building one of the world’s most trusted technology and supply chain ecosystems. What started as a bold idea in China has evolved into a NASDAQ-listed,
About the company: Jambo Zorg Lokaal is a specialized branch of Jambo that focuses entirely on the Dutch healthcare market. We supply pharmacies, hospitals, residential care centers, and nursing homes with a wide range of high-quality
Functietitel– Supplier Quality & Raw Material Qualification Intern Locatie– Maastricht, The Netherlands As a Raw Material Qualification Intern, you will support the Global Raw Material Qualification / Supplier Quality team in maintaining high standards of quality
As a Chargebacks Expert, you will play a key role in protecting our users by ensuring Mastercard disputes are handled accurately, fairly, and in line with Mastercard and PSD2 requirements. Taking end-to-end ownership of the chargeback
ABOUT US: Gisou is born out of a passion for bees and haircare, based on a six-generation beekeeping heritage, our products are inspired by and made with the finest, sustainably sourced ingredients from our very own
Job Overview Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Please note: for
Company Overview DeepHealth, a RadNet company, is focused on delivering AI-powered solutions that improve population health, optimize radiology workflows, and drive earlier detection of disease. Our portfolio spans breast, lung, brain, prostate, and thyroid imaging AI,
Bedrijfsomschrijving Working at Boskalis is about creating new horizons and sustainable solutions. In a world where population growth, increase of global trade, demand for (new) energy and climate change are driving forces, we challenge you to
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 Overview Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Please note: for
At bunq, we dont solve growth by hiring more people. We solve it by building smarter systems. As our Reporting Expert, youll transform regulatory reporting into an AI-powered one. Youll design the decision logic, reporting frameworks, and
Do you want your voice heard and your actions to count? Discover your opportunity with Mitsubishi UFJ Financial Group (MUFG), one of the world’s leading financial groups. Across the globe, we’re 150,000 colleagues, striving to make