Regulatory Affairs Specialist

Benefits

Parental leave

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Non-birth-parent leave

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Family-building benefits

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Mental health support

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Childcare support

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Role

Seniority

Mid From the posting source

Schedule

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Weekend work

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Company

Equity

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Application

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Deadline

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About this role

Regulatory Affairs Specialist Athlone About Teleflex Incorporated As a global provider of medical technologies, Teleflex is driven by our purpose to improve the health and quality of people's lives. Through our vision to become the most trusted partner in healthcare, we offer a diverse portfolio with solutions in the therapy areas of anesthesia, emergency medicine, interventional cardiology and radiology, surgical, vascular access, and urology. We believe that the potential of great people, purpose-driven innovation, and world-class products can shape the future direction of healthcare. Teleflex is the home of Arrow™, Barrigel™, Deknatel™, LMA™, Pilling™, QuikClot™, Rüsch™, UroLift™ and Weck™ - trusted brands united by a common sense of purpose. At Teleflex, we are empowering the future of healthcare. For more information, please visit teleflex.com. Position Summary Support the regulatory activities which lead to and maintain regulatory compliance and approval for Teleflex Medical products in the EMEA region Principal Responsibilities Key responsibilities will include (but are not limited to) the following: • Ensure compliance with EMEA regulatory requirements and applicable regulatory standards. • Coordinate and support regulatory and product registration activities for the EMEA region, including new product registrations, license amendments, renewals, and maintenance of existing approvals. • Prepare, compile, review, and maintain regulatory submission files and associated documentation for product registrations

Read the full description at careers.teleflex.com. FewerJobs shows a preview and links to the original posting.