Regulatory Scientist, Vascular

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🕒 Setembro 23

🇺🇸 Estados Unidos – Remoto (EUA)

⏰ Tempo Integral

🟡 Pleno

🟠 Sênior

🚔 Conformidade

👻 Score fantasma 14%

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🗣️🇺🇸🇬🇧 Inglês obrigatório

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Cook Group

11 - 50 funcionários

🏥 Saúde

💼 Consultoria

📦 Logística

Healthcare • Consulting • Logistics

Cook Group é um conjunto de empresas éticas e empreendedoras que existe para capacitar pessoas e comunidades a alcançarem seu pleno potencial. Enraizada em dispositivos médicos, a empresa também atua no setor de ciências da vida e se envolve em gestão de propriedades, resorts e negócios de serviços. Com sede em Indiana e presença mundial, a Cook Group valoriza integridade, qualidade, respeito e transparência, guiando seu trabalho e relacionamentos com funcionários, clientes e comunidades.

Descrição

• Fulfill premarket and post-market regulatory requirements for medical devices manufactured by Cook Group companies • Coordinate with cross-functional teams to develop strategies for new medical devices and support existing devices • Maintain knowledge of medical-device regulations and assess their impact on projects • Learn new technical subjects and communicate technical and scientific information to project teams and regulatory authorities • Coordinate with the Director of Regulatory Science to understand goals and priorities, develop project plans, and facilitate project progress • Assess new technologies for regulatory pathways • Collaborate with Business Units, Engineering, Clinical, and Marketing to develop and implement scientifically sound regulatory strategies • Provide scientific review and regulatory guidance throughout projects, including non-clinical and clinical strategy development • Review non-clinical and clinical data for accuracy, completeness, and submission suitability • Write or coordinate clear regulatory documents and submissions to global regulatory authorities • Provide technical, scientific, and regulatory leadership for new-device approvals and maintenance of marketed-device approvals • Review change requests for supporting-data adequacy and reporting requirements • Travel as necessary to support projects

🎯 Requisitos

• Master's degree or PhD in a scientific or an engineering discipline, or equivalent medical device industry/regulatory experience • Familiarity with applicable regulatory requirements and regulatory submissions, including IDEs, PMAs, 510(k)s, Clinical Evaluation Reports, and other global regulatory documents • Excellent technical and problem-solving skills • Ability to effectively communicate in both spoken and written form • Familiarity with statistical methods, analysis, and interpretation • Ability to work on multiple projects, organize, and prioritize within time constraints • Familiarity with Microsoft Office software • Commitment to participate in a team-based environment • Fluency in Artificial Intelligence (AI) and data concepts, including critically evaluating AI outputs, improving workflows using approved tools, identifying and mitigating bias or inaccuracies, and communicating AI-driven insights clearly and responsibly • Legally authorized to be employed in the United States • No employment visa sponsorship provided

🏖️ Benefícios

• Fully remote positions are available • Option to work at the West Lafayette, IN or Bloomington, IN Cook facilities • Equal employment opportunity employer

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