The Regulatory Affairs Specialist II, will provide administrative and technical support to regulatory affairs leadership in order to facilitate compliance with U. The Regulatory Affairs Specialist pro...

Provide regulatory guidance to cross-functional teams and develop global regulatory strategies. Prepare and submit regulatory documents for US and OUS regulatory filings. Regulatory Affairs Certificat...

Regulatory Affairs Specialist will work within Regulatory Affairs and with cross functional teams to lead RA efforts for Dexcom’s SaMD products. Regulatory Affairs Specialist will work with software, ...

The Regulatory Affairs Specialist II, will provide administrative and technical support to regulatory affairs leadership in order to facilitate compliance with U. The Regulatory Affairs Specialist pro...

Senior Regulatory Affairs Specialist. Senior Regulatory Affairs Specialist – Cardiac Rhythm Management (on-site). Certification is a plus (such as RAC from the Regulatory Affairs Professionals Society...

Senior Regulatory Affairs Specialist. Master’s Degree in Regulatory Affairs and may be used in lieu of direct regulatory experience. Acts as a regulatory representative on core product development tea...

The Principal Regulatory Affairs Specialist will understand the regulations governing medical devices and will be responsible for assessing changes to medical devices and products or processes to dete...

The Regulatory Affairs Specialist III, will provide administrative and technical support to regulatory affairs leadership in order to facilitate compliance with U. The Regulatory Affairs Specialist pr...

The Regulatory Affairs Specialist II, will provide administrative and technical support to regulatory affairs leadership in order to facilitate compliance with U. The Regulatory Affairs Specialist pro...

The Regulatory Affairs Specialist II, will provide administrative and technical support to regulatory affairs leadership in order to facilitate compliance with U. The Regulatory Affairs Specialist pro...

Senior Regulatory Affairs Specialist. Master's Degree in Regulatory Affairs and may be used in lieu of direct regulatory experience. Provides mentoring and leadership to Regulatory Specialist I and II...

Seeking a Principal Regulatory Affairs Specialist to support the Kindeva business in maintaining regulatory compliance of existing manufactured products for customers on a global basis by:. Managing r...

Regulatory Affairs Specialist/Manager will oversee medical device development and market introduction, ensuring compliance with regulatory standards for Class I, II, and III devices. A minimum of 5 ye...

The Senior Regulatory Specialist is responsible to plan, direct and coordinate global product registrations and lead regulatory submissions planning and execution; collaborate with Product Regulatory ...

Thorough knowledge of policies, practices and procedures related to Regulatory Affairs. Reg Affairs, QA, R&D, Manufacturing, and/or Project Management within the IVD industry.

He/She has responsibility for compliance with US and EU regulatory requirements and partners with the international regulatory affairs group to support regulatory submissions. Minimum of 7 years of ex...

The role of the Regulatory Affairs Specialist will be to support the global regulatory affairs of the business with a specialized focus on the United States. Lead regulatory strategy and submissions t...

From design to production, our Regulatory Affairs teams help guide our innovative technologies through complex domestic and international regulatory environments. Represent the regulatory function on ...

Participate in representing the OUS regulatory function on manufacturing and product development teams to provide input on regulatory requirements, including presenting alternatives for meeting regula...

The Sr Regulatory Affairs Specialist is responsible for ensuring digital medical device regulatory clearance to enable market access by demonstrating compliance to applicable regulations through a reg...