USA remote
Principal Regulatory Affairs Specialist
About this role
What Regulatory Affairs contributes to Cardinal Health Regulatory provides regulatory affairs and product development consulting services to enable pharmaceutical, medical and biotechnology companies to obtain regulatory approvals. This function applies subject matter expertise to provide services in technical writing and regulatory submissions as well as clinical research and manufacturing process consulting. Regulatory Affairs plans, coordinates and implements regulatory strategies for products that require government approval.
This job family proactively identifies regulatory requirements and risks for products and develops plans for product development programs and regulatory submissions. Job Summary The Principal Regulatory Affairs Specialist will support the Medical Solutions Regulatory affairs team. They are responsible for regulatory activities associated with new product development and maintenance of business projects. This includes being a regulatory lead for change development projects, new product development, change assessment, US, EU and international regulatory submissions, commercial support, manufacturing support, compliance related activities, systems improvement, and other responsibilities aligned with global medical device regulations and the goals of the Medical Solutions business.
Location: This is a remote position, and the ideal candidate will be located near or willing to travel to Waukegan, IL or Mansfield, MA. Responsibilities Lead new and modified product development projects to establish and integrate regulatory strategy into project activities. Lead the preparation, submission, and maintenance of global product registrations with a focus on 510(k), EU Technical Documents, and International STEDs.
Collaborate with internal Cardinal Health international regulatory departments to assess international registration requirements, develop international regulatory strategy, and ensure timely execution. Review design control documents including documents associated with design inputs and design outputs. Review product labeling for compliance with global labeling regulations. Interpret and evaluate proposed regulations for medical devices and advise on impact of such regulations to the business.