Deborah Stubbs Email & Phone Number | Ten years in UL LLC Health Sciences product safety for medical devices, IEC 60601-1 its collateral and particular standards. Moved to Regulatory in 2006 continued to act as final review for product safety until 2015. Moved to the Principal Engineering Group March 2023. Moved to the Principal Engineering Group March 2023 acting as technical expert for UL Solutions Regulatory Business Unit and Regulatory Standards Development (ISO/CASCO). Responsible for auditor and technical reviewer training and qualification. Responsible for regulatory program development including Software IEC 62304 and Risk Management ISO 14971 , ISO 13485 and MDSAP. Regulatory and Technical Expert for Medical Software, EN 62304, MD 1111, MDS 7010, MDS 7210. Lead auditor for MDD, MDSAP, 13485, 9001 for active and non-active medical devices and software.

Deborah Stubbs

Ten years in UL LLC Health Sciences product safety for medical devices, IEC 60601-1 its collateral a...
San Jose, California, United States

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Deborah Stubbs’s Email deborah.stubbs@ul.com

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Deborah Stubbs’s Location San Jose, California, United States

Deborah Stubbs’s Current Industry Ul Solutions

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Principal Engineer (PrE)

2023-03-01 00:00:00 - Present

Lead Regional Lead Reviewer

1998-06-01 00:00:00 - 2023-03-01 00:00:00

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Deborah Stubbs is a Ten years in UL LLC Health Sciences product safety for medical devices, IEC 60601-1 its collateral and particular standards. Moved to Regulatory in 2006 continued to act as final review for product safety until 2015. Moved to the Principal Engineering Group March 2023. Moved to the Principal Engineering Group March 2023 acting as technical expert for UL Solutions Regulatory Business Unit and Regulatory Standards Development (ISO/CASCO). Responsible for auditor and technical reviewer training and qualification. Responsible for regulatory program development including Software IEC 62304 and Risk Management ISO 14971 , ISO 13485 and MDSAP. Regulatory and Technical Expert for Medical Software, EN 62304, MD 1111, MDS 7010, MDS 7210. Lead auditor for MDD, MDSAP, 13485, 9001 for active and non-active medical devices and software.