Vice President, Clinical Development and Trial Innovation
with digital health providers in the US, EU, and Asia to streamline and accelerate trial data collection and scale the cross...
with digital health providers in the US, EU, and Asia to streamline and accelerate trial data collection and scale the cross...
compliance for product development process and sustaining engineering projects, ensuring compliance with FDA and EU regulations..., ISO standards, and other regulatory agencies Coordinate, compile, and submit US and EU regulatory filings for new...
, HIPAA/HITECH, FFIEC, EU Privacy Laws, ISO, and NIST 800 series Experience in the financial services and/or financial...
, and other job opportunities at GOAT Group. If you are a California resident, please review our . If you are an EU or UK resident, please review our...
Level 6 or equivalent EU Qualifications & Experience: Minimum of 4 years in a Quality/Regulatory Affairs environment...
. Confirm labeling content and artwork alignment with FDA 21 CFR 801, EU MDR Annex I (GSPR 23), ISO -1, ISO, UDI/GS1, and IEC/UL... technologies for capital and reusable equipment. Working knowledge of FDA 21 CFR 801, EU MDR GSPR 23, ISO -1, ISO, UDI/GS1...
and project specifications. SGRE is based in Orlando, USA, you can however be deployed to projects worldwide including (EU...
Can be remote or on-site Key Responsibilities: Support US and EU regulatory submissions (exercising judgment...
governance frameworks aligned to standards such as NIST AI RMF, ISO/IEC 42001, and EU AI Act guidance Translate technical...
governance frameworks aligned to standards such as NIST AI RMF, ISO/IEC 42001, and EU AI Act guidance Translate technical...