Merit Medical Oncology
5001 - 10000 employees
Founded 1987
🤝 B2B
💰 $4.2M Venture Round - Cianna Medical on 2016-10
B2B
Merit Medical Oncology is a division/specialty of Merit Medical Systems focused on devices and procedural solutions for oncologic interventions. It is part of Merit Medical Systems, a global manufacturer founded in 1987 that designs and markets proprietary disposable medical devices used in interventional, diagnostic and therapeutic procedures across cardiology, radiology, oncology, critical care and endoscopy. Merit Medical Oncology supports hospitals and physicians worldwide with products (e. g. , biopsy, embolotherapy, drainage, and other oncology-related interventional tools), clinician education and training, regulatory and product documentation, and global distribution and customer support.
Senior Regulatory Specialist – Bilingual (French/English)
Job not on LinkedIn
🔥 1 hour ago
🗣️🇫🇷 French Required
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Merit Medical Oncology
5001 - 10000 employees
Founded 1987
🤝 B2B
💰 $4.2M Venture Round - Cianna Medical on 2016-10
B2B
Merit Medical Oncology is a division/specialty of Merit Medical Systems focused on devices and procedural solutions for oncologic interventions. It is part of Merit Medical Systems, a global manufacturer founded in 1987 that designs and markets proprietary disposable medical devices used in interventional, diagnostic and therapeutic procedures across cardiology, radiology, oncology, critical care and endoscopy. Merit Medical Oncology supports hospitals and physicians worldwide with products (e. g. , biopsy, embolotherapy, drainage, and other oncology-related interventional tools), clinician education and training, regulatory and product documentation, and global distribution and customer support.
📋 Description
• Exemplify an engaged culture aligned with the Merit Way • Collaborate with RA Platform teams for product submissions • Manage regulatory license portfolio and compliance • Support continuous improvement of resource planning • Develop training materials and programs for stakeholders
🎯 Requirements
• Education equivalent to Bachelor’s degree in biological, physical, engineering, or related fields • 8+ years of Regulatory Submissions experience in the medical device industry • Deep knowledge of medical device regulations, including ISO 13485 • Project management skills
🏖️ Benefits
• Health insurance • Professional development
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