FDA Resumes

Denver, CO
... Certifications Infection Control in Health Care Cleaning (8/2025) SQF Practitioner (2020) HACCP Certified (2020) GMP – Good Manufacturing Practices in Sanitation Certificate (2020) Sanitation Practices II –FDA – (2020) Six Sigma Certification – ... - Feb 06

Anderson, SC
... Administering Injections • Cardiac arrest emergency response • Customer retention • Packaging • Box truck • Quality systems • FDA regulations • Client interaction via phone calls • Manufacturing facility • Visual merchandising • Cash handling • ... - Feb 06

Kaufman, TX
... Monitored and tracked inventory of fresh and frozen products to ensure compliance with FDA, USDA, and HACCP regulations. Equipment Maintenance: Planned and scheduled preventive and routine maintenance of manufacturing equipment to maximize ... - Feb 06

Louisiana
... • Time management • Grocery store • Kitchen experience • Project management • Serving (10+ years) • Sales (10+ years) • FDA regulations • Continuous improvement • Food industry • Food service • Communication skills (10+ years) • Administrative ... - Feb 05

Texas
... Identified, initiated, monitored and close out investigational sites in accordance with standard operating procedures (SOPs) and FDA guidelines. • Verified that the investigator and all research staff has adequate qualifications and resources and ... - Feb 05

California
... Proven ability to design, execute, and manage comprehensive test plans in alignment with FDA (21 CFR Part 820) and ISO 13485 standards. Adept at collaborating with cross-functional teams, performing firmware and cloud-based application testing, and ... - Feb 05

Sunnyvale, CA
... Core Competencies ● Global Market Access: Extensive experience spearheading submissions across major markets including the US (FDA), EU (MDR/IVDR), and Canada (Health Canada), as well as emerging markets in APAC, EMEA, and LATAM. ● Technical ... - Feb 05

East Brunswick, NJ, 08816
... • Prepared and submitted over 30 regulatory submissions, including FDA 510(k) applications for Class I and II medical devices, ensuring compliance with 21 CFR Part 820 regulations. • Authored, reviewed, and approved Product Quality Complaint (PQC) ... - Feb 05

Laurel, MD
... Food and Drug Administration (FDA) Silver Spring, MD August 2015– November 2018 Office Automation Clerk Used Microsoft Word to compose and edit standard documents, correspondence and emails for the Director, Program Management Office (PMO), Center ... - Feb 05

White Oak, PA, 15131
... ●Provided training programs, staff educational in-services, safety leadership, health, environmental, including compliance and regulatory issues (i.e., FDA, OSHA, EPA) and updates to current and new employees. Additional Relevant Experience Sunoco ... - Feb 04