QA & Regulatory Affairs Lead - Medical Devices

Regulatory Affairs Specialist – Medical Devices The Regulatory Affairs Specialist is responsible for preparing, submitting, and maintaining regulatory documentation to support global approvals of high‑risk or implantable medical devices. This role ensures compliance with U.S. FDA regulations, EU MDR 2017/745, and other international requirements,...

Regulatory Affairs Specialist – Medical Devices The Regulatory Affairs Specialist is responsible for preparing, submitting, and maintaining regulatory documentation to support global approvals of high‑risk or implantable medical devices. This role ensures compliance with U.S. FDA regulations, EU MDR 2017/745, and other international requirements,...

Global Medical Affairs Director Position at Novartis. Summary The Global Medical Affairs team serves as the organization’s medical voice throughout the asset lifecycle and leads strategy for the therapeutic area. They develop and oversee the Integrated Evidence Plan (IEP), ensuring both US and international medical perspectives are considered during...

**LAR-2411-365** **REGULATORY AFFAIRS ASSOCIATE DIRECTOR** **MADRID** **Regulatory Affairs Associate Director Opportunity - Join a Leading Pharmaceutical Company in Madrid, Spain!** At **MCR International**, we're thrilled to announce an exclusive opportunity for a **Regulatory Affairs Associate Director** with a **renowned global pharmaceutical company**....

At ORBIK CYBERSECURITY, S.COOP, a leading company in product cybersecurity solutions, we are looking for a **Regulatory Affairs Manager** to lead the management of regulations and standards in the industrial cybersecurity sector. This position is crucial to ensuring that our operations, products, and services comply with the most stringent international...

BettingJobs is working with a well established multi‑vertical iGaming group seeking to expand their fully remote team with an experienced Licensing and Regulatory Affairs Manager. This role has a strong reference for those based in Cyprus. This role is critical in ensuring our group of companies operates with the correct licences and regulatory approvals...

Oportunitat laboral. Eignapharma, empresa de serveis a la Indústria Farmacèutica ubicada al Tecnocampus de Mataró, cerca cobrir una posició de tècnic al departament de Regulatory Affairs. Descripció de la posició: Revisió, preparació i presentació d'expedients per l'obtenció d'autoritzacions de comercialització a Europa, procediments nacional,...

Join to apply for the Medical Advisor, Spain role at Revolution Medicines . Revolution Medicines is a clinical‑stage precision oncology company focused on developing novel targeted therapies to inhibit frontier targets in RAS‑addicted cancers. The company’s R&D pipeline comprises RAS(ON) Inhibitors designed to suppress diverse oncogenic variants of RAS...

Medical Director, Ophthalmology (Clinical Development) MD or PhD required | Ophthalmology experience essential We are seeking a senior Medical Director with deep ophthalmology experience to lead global clinical development programs in this space. This is a high-impact leadership role responsible for defining and executing clinical strategy across...

Due to our ongoing global expansion, we have a great opportunity for a Regulatory Submissions Specialist to join our growing regulatory team in Taiwan, on a fully remote basis.We are looking for someone who can autonomously carry on the work within the scope of their activities and interacts with the Direct Manager to define priorities and manages workload....