
Florian
ISO Compliance, Medical Device Regulatory, Food Safety Documentation Expert
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Portfolio
Work experience
Senior Regulatory Affairs Consultant
GHA Foundation • Freelance
Jan 2021 - Jul 2026 • 5 yrs 6 mos
Lead regulatory compliance projects for medical device manufacturers, healthcare organizations, and startups. Prepare Technical Documentation, Technical Files, Clinical Evaluation Reports (CER), Risk Management Files, FDA submissions, CE MDR documentation, ISO 13485 Quality Management Systems, and regulatory strategies. Support clients through product development, market access, certification readiness, and post-market compliance while ensuring alignment with global regulatory requirements.
ISO Management Systems Consultant
Juno Media • Freelance
May 2019 - Jul 2026 • 7 yrs 2 mos
Designed and implemented Quality Management Systems for organizations across manufacturing, healthcare, engineering, logistics, and technology sectors. Developed Quality Manuals, SOPs, Procedures, Risk Registers, CAPA, Internal Audit Programs, Management Review documentation, and certification-ready systems for ISO 9001, ISO 14001, ISO 45001, ISO 27001, ISO 22000, and Integrated Management Systems.
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macleender
Repeat Client

United States
This is my second project with Esmeralda, and once again she exceeded expectations! She handled my BOI report filing and compliance support quickly, professionally, and with great attention to detail. Her communication was excellent, the turnaround was very fast, and she made the entire process seamless....

macleender
Repeat Client

United States
Esmeralda went above and beyond my expectations! She handled my LLC formation and EIN application with exceptional professionalism, accuracy, and speed. The turnaround was incredibly fast, communication was excellent, and she made the entire process smooth and stress-free. I highly recommend her services...
