Brian Johnson Email & Phone Number | I support the launch and maintenance of Medical Devices and SaMD's in the US, EU, Canada, Australia and ROW. I am currently directing regulatory strategy in the US and other markets for a Class II implantable medical device with Software as Medical Device (SaMD) components. I have experience preparing 510k submissions in the US, MDR/IVDR submissions for the EU, Canada, Australia, Japan, and some South American countries. My most recent focus has been SaMD and software development compliance with IEC 62304, IEC 62366, and AAMI TIR45:2012. As a leader I have built teams and led teams. As a contributor I enjoy collaborating with people across different departments in an organization and I am passionate about lifting people up and improving processes.

Brian Johnson

I support the launch and maintenance of Medical Devices and SaMD's in the US, EU, Canada, Australia...
Rock Hill, South Carolina, United States

*50 free lookup(s) per month.

Brian Johnson’s Phone Numbers

Get BRIAN’s Phone Number (For Free)

Social Media

Brian Johnson’s Location Rock Hill, South Carolina, United States

Brian Johnson’s Current Industry Canary Medical

Find accurate emails & phone numbers for over 700M professionals.

Senior Regulatory Affairs Specialist

2022-09-01 00:00:00 - Present

Senior Regulatory Affairs Specialist

2021-04-01 00:00:00 - 2022-09-01 00:00:00

Senior Regulatory and Compliance Specialist

2019-12-01 00:00:00 - 2021-04-01 00:00:00

Quality Systems Supervisor

2016-01-01 00:00:00 - 2019-12-01 00:00:00

Quality Assurance and Regulatory Affairs Specialist

2013-09-01 00:00:00 - 2016-01-01 00:00:00

Quality Assurance & Technical Support Specialist

2007-08-01 00:00:00 - 2011-07-01 00:00:00

Lead Validation Specialist

2006-07-01 00:00:00 - 2007-08-01 00:00:00

No Skills Available

No Languages Available

Brian Johnson is a I support the launch and maintenance of Medical Devices and SaMD's in the US, EU, Canada, Australia and ROW. I am currently directing regulatory strategy in the US and other markets for a Class II implantable medical device with Software as Medical Device (SaMD) components. I have experience preparing 510k submissions in the US, MDR/IVDR submissions for the EU, Canada, Australia, Japan, and some South American countries. My most recent focus has been SaMD and software development compliance with IEC 62304, IEC 62366, and AAMI TIR45:2012. As a leader I have built teams and led teams. As a contributor I enjoy collaborating with people across different departments in an organization and I am passionate about lifting people up and improving processes.

Brian Johnson has prior
experience in the following industries:
Lifescan | Monarch Medical Technologies | Csl Plasma | Hartmann Usa | American Red Cross | Leiner Health Products

Brian Johnson has the following professional experience:
Canary Medical | Lifescan | Monarch Medical Technologies | Csl Plasma | Hartmann Usa | American Red Cross | Leiner Health Products