Terumo Neuro · 11 hours ago
Intern, Regulatory Affairs
Terumo Neuro is a high-growth company focused on producing reliable and technologically advanced products. The Regulatory Affairs Intern will learn about the product development process from a regulatory perspective and assist in obtaining regulatory approvals for products.
Medical Device
Responsibilities
Familiarize with the design, manufacture, and the clinical use of the Terumo Neuro products
Perform specific regulatory tasks in support of a regulatory filing for new/modified product and any planned renewal of regulatory registrations (FDA, EU or Health Canada)
Partner and collaborate with R&D, Operations, Quality, Labeling, and Marketing to help establish project deliverables to support regulatory submissions
Shadow and/or partner with a senior regulatory professional(s) to learn and interpret regulations and implement them on the assigned project(s)Learn regulatory affairs competencies to ensure product registration lifecycle processes compliance
Performs other duties and responsibilities as assigned
Qualification
Required
Working toward Master's degree in Regulatory Affairs or related field
Demonstrates a working understanding of regulations
Excellent written, verbal and interpersonal communication and computer skills
Proven analytical abilities and ability to comprehend technical documents and concepts
Ability to work independently and manage multiple priorities effectively
Company
Terumo Neuro
We’re in business to create and deliver innovations that redefine what’s possible in neurovascular treatment, meaningfully advancing both physician practice and patient outcomes.
Funding
Current Stage
Late StageCompany data provided by crunchbase