- Kuehne+Nagel (Seatac, WA)
- …merchandise through US. Customs & Border Protection; PGA's (Participating Governmental Agencies ie FDA , EPA, DOT, FCC, Fish and Wildlife ) **The Work Location would ... necessary import documentation from client + Accurate completion of all PSG data interfaces (ie FDA , EPA, DOT, FCC, Fish & Wildlife etc ) and communicate entry # and… more
- Adecco US, Inc. (Caguas, PR)
- …+ Solicitar y verificar pruebas de laboratorio, monitorear cambios en regulaciones de FDA y otras agencias, y mantener licencias al dia. + Administrar inspecciones y ... compra de bienes al detal** . + Conocimiento de regulaciones y estandares de ** FDA ** y otras agencias aplicables. + Dominio avanzado de **MS Office** . + **Bilingue… more
- Cedars-Sinai (Los Angeles, CA)
- …study budget and patient research billing. Ensures compliance with all federal, local, FDA , IRB, and HIPAA guidelines and regulations pertaining to the study and ... with all federal and local agencies including the Food and Drug Administration ( FDA ) and local Institutional Review Board. + Maintains research practices using Good… more
- BrightSpring Health Services (Groveport, OH)
- …for supporting Quality Assurance (QA) activities in compliance with FDA /DEA/State Regulations, cGMP, and company policies, procedures and specifications at ... metrics + Assists in the GMP auditing program for internal and external ( FDA , DEA, and State) audits + Supports the development, continuous improvement, and… more
- Cayuse Holdings (Phoenix, AZ)
- …for Healthcare Interpreters + Experience with State Department experience/ refugees, FDA , Health & Human services, Medical, Legal, Housing Authority etc. + ... or translation experience in Popti language + State Department experience/ refugees, FDA , Health & Human services, Medical, Legal, Housing Authority etc. + Must… more
- Mentor Technical Group (Caguas, PR)
- …monthly Quality Review meetings. * Assists in gathering of information during FDA inspections, Notified Body Audits, Corporate Audits, etc. Performs other position ... order to meet the requirements of all applicable Quality System regulations (eg: FDA Part 820 Quality System Regulation, ISO 13485 Quality Standard, R-PAL (Japanese… more
- PCI Pharma Services (Bedford, NH)
- …oral, and good written communication skills. + Knowledge of GMP and FDA regulatory requirements for drugs and/or medical devices. + Excellent communication skills ... SolidWorks, PLC & SCADA control system. + Experience working in a GMP and FDA regulatory environment for drugs and/or medical devices a plus. + Plant Engineering… more
- Sutter Health (Sacramento, CA)
- …privacy, and clinical safety risks. -Ensure compliance with HIPAA, HITECH, CMS, FDA (for medical device security), and state privacy regulations. -Oversee security ... & Skills** + Deep knowledge of HIPAA, HITECH, CMS, OCR enforcement, FDA guidance for medical devices, and healthcare-specific risk management frameworks. + Expertise… more
- Edwards Lifesciences (Irvine, CA)
- …MEDDEV 2.7/1 and EU MDR for clinical evaluations. + Familiarity with FDA PMA applications. + Good knowledge of scientific research methodology, device development ... process, GCP, ICH guidelines and Global (US FDA , EU MDR) regulations. + Experience working in a cross functional, collaborative environment and comfortable… more
- Ultradent Products Inc (Salt Lake City, UT)
- …project life cycle, interpreting situations/ issues into compliant paths with regards to FDA , ISO, and Oratech standards. + Oversee updates to design history files ... + Strong understanding of regulatory guidance relevant to medical device, specifically FDA 's CFR820.30 and ISO 13485:2016 + 1-3 years of experience leading… more