Door categorieën bladeren
Ontdekken
Fiverr Pro
Nederlands
$
USD
Josephine Matt
@josephine7482
FDA Compliance Expert, US Agent, FSVP, 510k, Import Clearance Specialist
Verenigde Staten
Engels
Over mij
Entering the U.S. market requires more than just FDA registration, it requires getting it right with the right expert like myself. I help international brands and manufacturers navigate FDA compliance for food, cosmetics, supplements, and medical devices with accuracy and clarity.
From FDA Facility registration and U.S. Agent support to FSVP, Prior Notice, labeling, and device listing/510(k), I ensure your product meets FDA requirements and clears import smoothly. Reliable, compliant, and handled the right way from day one. SEND A MESSAGE NOW OR PLACE AN ORDER TO GET STARTED, THANKS.
Skills
Josephine Matt
offline •
Gemiddelde reactietijd: 1 uur
Bekijk mijn diensten
Bedrijfsregistratie
I will do fda registration, mocra cosmetic listing, and product compliance
Inkoop- en leveranciersbeheer
I will fda registration compliance assistance for food, drug, and medical devices
Werkervaring
Regulatory Compliance Specialist
Pfizer • Fulltime
Apr 2026 - Present • 1 mo
Worked on FDA compliance processes, labeling review, and regulatory documentation foLed FDA regulatory strategy for product approvals across food, cosmetics, and medical devices. Managed facility registrations, labeling compliance, and 510(k) submissions. Ensured full adherence to FDA regulations, supporting seamless U.S. market entry and successful import clearance for multiple product lines.
FDA Compliance & Quality Specialist
Abbott • Fulltime
Jan 2020 - Aug 2023 • 3 yrs 7 mos
Handled FDA facility registration, product listing, and GMP compliance for healthcare and consumer products. Performed internal audits, risk assessments, and quality documentation to maintain regulatory standards. Assisted with import compliance and inspection readiness.
Regulatory Affairs Associate
Johnson & Johnson • Fulltime
May 2021 - Apr 2023 • 1 yr 11 mos
Supported FDA submissions including medical device listing, UDI compliance, and documentation for 510(k) clearance. Conducted regulatory research and labeling reviews to ensure compliance with FDA and global standards. Collaborated with internal teams to streamline approval timelines.
