VP Regulatory Affairs - Caesarea, Haifa District

+Job summary · The VP RA/QA leads global Regulatory Affairs and Quality Assurance activities, ensuring compliance with applicable regulations while supporting newly launched commercial operations and international expansion. · +ResponsibilitiesMaintain compliance with FDA require ...

We are seeking a detail-oriented Clinical Affairs Coordinator to support clinical trials for our IVD medical devices in semen analysis. · Support the design and execution of clinical studies involving semen analysis IVDsAssist in coordinating IRB approval process: participate in ...

אחראי/ת רגולציה זרה / החטיבה לניהול סיכונים. · ל-Unit of Compliance in Bank that operates on foreign regulation , is required to Regulatory affairs manager for a role that includes responsibility on CROSS BORDER and QI areas. · ...

We are seeking a Regulatory Affairs Specialist to join a leading global medical device company. This role includes ownership of regulatory submissions, technical documentation, and change management within multidisciplinary systems involving hardware, software, and invasive medic ...

+We are seeking a Regulatory Affairs Specialist to join a leading global medical device company. · +Lead end-to-end regulatory submissions, including technical documentation, change submissions, and authorizing regulatory files for global markets. · ...

The Director of Regulatory Affairs Informatics leads regulatory strategy and execution for software-enabled solutions, both device and non-device across areas like PACS, radiology, cardiology, pathology, · urology, · virtual care.The role ensures compliance with FDA, ...

Join Our Team at Bonus BioGroup – Regulatory Affairs PM. We are looking for a highly motivated and detail-oriented Regulatory Affairs Project Manager to join our Regulatory Affairs team. · ...

Dormotech Medical Ltd. is a digital health company revolutionizing the diagnosis and monitoring of sleep disorders through its innovative DormoVision X solution. · This is a full-time on-site role for a Regulatory Affairs Specialist, · based in Raanana. The Regulatory Affairs Spe ...

+We are seeking a Regulatory Affairs Specialist to join a leading global medical device company. · This role includes ownership of regulatory submissions, technical documentation, and change management within multidisciplinary systems involving hardware, software, and invasive me ...

The Director of Regulatory Affairs Informatics leads regulatory strategy and execution for software-enabled solutions, · both device and non-device across areas like PACS, radiology, cardiology, pathology, · urology, and virtual care. ...

This is a full-time on-site role for a Regulatory Affairs Specialist located in Raanana. · The Regulatory Affairs Specialist will be responsible for creating managing regulatory documentation ensuring compliance with applicable regulations and maintaining up-to-date knowledge of ...

We are seeking an experienced VP Regulatory Affairs to lead global regulatory strategy for cutting-edge products and drive successful submissions across major health authorities. · Advanced degree (MSc / PhD) in Life Sciences, Pharmacy, or a related fieldProven track record of su ...

This is a full-time on-site role for a Regulatory Affairs Specialist, · The candidate will work closely with cross-functional teams to ensure adherence to national and international regulatory standards.Lead and maintain compliance with ISO 13485 Quality Management System · Suppo ...

Regulatory Affairs Manager to lead regulatory strategies for crop protection products and develop dossiers. · ...

We are looking for out-of-the-box thinkers, people who are passionate, caring, agile and adaptive,to join us on our mission. · Preparing registration portfolios (new,renewal,and update) for submission to the MOH,and updating tracking charts for each product. · Coordinating delive ...

Medison offers hope to patients suffering from rare and severe diseases, by forming partnerships with emerging biotech companies to accelerate access to highly innovative therapies in international markets. · As the creator and leader of the global partnership category in the pha ...

We are looking for out-of-the-box thinkers to join us on our mission to make a difference in people's lives. · ...

Medison offers hope to patients suffering from rare and severe diseases by forming partnerships with emerging biotech companies. · ...

We are seeking a highly analytical and detail-oriented Regulatory-related Projects Manager with a strong legal background to join our global regulation team. In this role, you will be a key driver in ensuring our multi-jurisdictional operations remain compliant with evolving CFD ...

We are seeking a highly analytical and detail-oriented · Regulatory-related Projects Manager with a strong legal background to join our global regulation team. · User Agreement (UA) Lifecycle: Lead the drafting, review, · and global rollout of updates to User Agreements and Term ...