Director of Regulatory Affairs - Haifa

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. ...

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. · ...

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 Terms of ...

Job summary · We are seeking a highly analytical and detail-oriented Regulatory-related Projects Manager with a strong legal background to join our global regulation team. · ...

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 ...

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 ...

+A successful medical device company seeks a Regulatory Affairs Specialist for its team. · + · +Ensure compliance with international regulatory requirements for medical devices · Support new product development processes from concept through launch · ,"valid_job":1} I have follo ...

+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. · ...

+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 ...

Job summaryA successful medical device company seeks a Regulatory Affairs Specialist to join its team. · ResponsibilitiesEnsure compliance with international regulatory requirements for medical devices · ...

+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 ...

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. · ...

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 ...

The Senior Regulatory Affairs Specialist is responsible for regulatory affairs support of submissions and ongoing regulatory compliance for product development & design changes processes. · At Boston Scientific, we'll give you the opportunity to harness all that's within you by w ...

This is a place where you can find meaningful purpose, improving lives through your life's work. In the Urology division, we continually advance the quality of patient care with innovative urology solutions. · ...

This is the job summary paragraph. · Provide technical and regulatory guidance to cross-functional teams throughout new product development and design changes. · Support the development and review of responses to non-conformances from Regulatory Authorities. · ...

+Job summary · The Systems Engineer has design responsibility to deliver customer workflow, feature functionality, product quality, reliability serviceability manufacturability regulatory compliance and cost. · +ResponsibilitiesProviding domain expertise to serve as the main inte ...

The PET V&V Manager will lead and oversee all Verification and Validation activities for Positron Emission Tomography (PET) systems and components, ensuring product quality, regulatory compliance, and successful product launches within GE HealthCare Israel. · ...

The PET V&V Manager will lead and oversee all Verification and Validation activities for Positron Emission Tomography (PET) systems and components, · Bachelor's degree in Biomedical Engineering, Electrical Engineering, Physics, or a related technical field. · Minimum of 8 years o ...