| Distance: | Resume alert | Resumes 81 - 90 of 25507 |
Insurance Access Specialist
Salem, WI
... and channel sources ● Identify potential Adverse Event situations for reporting to Pharmacovigilance to ensure AbbVie meets FDA regulations ● Train new hires and Insurance Specialists through side-by-side coaching, enabling team members to be more ... - Nov 28
... and channel sources ● Identify potential Adverse Event situations for reporting to Pharmacovigilance to ensure AbbVie meets FDA regulations ● Train new hires and Insurance Specialists through side-by-side coaching, enabling team members to be more ... - Nov 28
Tracee Freeman - Versatile Administrative & Sterile Processing
Ocklawaha, FL
... Followed OSHA, FDA and AAMI guidelines related to sterilization in compliance with administrative regulations. Collaborated with medical staff to confirm availability of medical equipment for patient care. Troubleshot medical equipment malfunctions ... - Nov 28
... Followed OSHA, FDA and AAMI guidelines related to sterilization in compliance with administrative regulations. Collaborated with medical staff to confirm availability of medical equipment for patient care. Troubleshot medical equipment malfunctions ... - Nov 28
Medical Laboratory Technician with Animal Diagnostics
Springfield, MA
... identifying red blood cell morphologies, platelet abnormalities, and blood parasites in 12+ species • Running samples from FDA-approved research experiments to assist with discovering proper treatment for animals PACKAGE DELIVERY DRIVER Vista, CA ... - Nov 28
... identifying red blood cell morphologies, platelet abnormalities, and blood parasites in 12+ species • Running samples from FDA-approved research experiments to assist with discovering proper treatment for animals PACKAGE DELIVERY DRIVER Vista, CA ... - Nov 28
Senior Analytical Laboratory Manager
North Scituate, RI
... • Lead of various laboratory projects for constant improvements to laboratory practices, workloads, and turnaround times • Laboratory lead for Client and FDA Audits September 2013 – September 2015 Finished Product Supervisor, Denison Pharmaceuticals ... - Nov 27
... • Lead of various laboratory projects for constant improvements to laboratory practices, workloads, and turnaround times • Laboratory lead for Client and FDA Audits September 2013 – September 2015 Finished Product Supervisor, Denison Pharmaceuticals ... - Nov 27
Senior .NET/SQL Developer with 24 Years IT Experience
Tampines, North East Community Development Counci, 521165
... redesigned ASP.NET pages of USDA’s eDRS and ColdFusion pages of FDA’s Watering Point and EPA’s DWTS to be Section 503 compliant developed/deployed web-pages, stored-procedures, functions and SQL-scripts for USDA FAS (ASP.NET/SQL-Server-2008R2) and ... - Nov 27
... redesigned ASP.NET pages of USDA’s eDRS and ColdFusion pages of FDA’s Watering Point and EPA’s DWTS to be Section 503 compliant developed/deployed web-pages, stored-procedures, functions and SQL-scripts for USDA FAS (ASP.NET/SQL-Server-2008R2) and ... - Nov 27
Hands-On IT Leader with Security Focus
Las Vegas, NV
... •Documented established practices (Policies, SOPs and SOX) standards for GRC requirements with the FDA, and audits to facilitate updates. •Merge hands on collaborative leadership style with excellent communication skills, (interpersonal and ... - Nov 26
... •Documented established practices (Policies, SOPs and SOX) standards for GRC requirements with the FDA, and audits to facilitate updates. •Merge hands on collaborative leadership style with excellent communication skills, (interpersonal and ... - Nov 26
Logistics Management, Procurement Management, Director of Logistics
San Carlos Park, FL, 33908
... • Oversaw global import/export documentation and regulatory compliance (IATA, FDA, HIPAA, DOT). • Monitored global inventories, retest dating, and proactively identified risks with corrective action plans. • Partnered cross-functionally with CMC, ... - Nov 26
... • Oversaw global import/export documentation and regulatory compliance (IATA, FDA, HIPAA, DOT). • Monitored global inventories, retest dating, and proactively identified risks with corrective action plans. • Partnered cross-functionally with CMC, ... - Nov 26
Seasoned Clinical Research Professional with FDA GCP Expertise
Hopkinton, MA
... Completed comprehensive training through Clinical Research Fastrack, gaining knowledge in FDA regulations, trial operations, informed consent, and site management. Passionate about contributing to high-quality, patient-centered studies that advance ... - Nov 26
... Completed comprehensive training through Clinical Research Fastrack, gaining knowledge in FDA regulations, trial operations, informed consent, and site management. Passionate about contributing to high-quality, patient-centered studies that advance ... - Nov 26
Regulatory Affairs Specialist with Medical Device Focus
West Roxbury, MA
... Skilled in FDA 510(k), ISO 13485, EU MDR, and PMS processes. Founder of an AI-powered compliance platform and Co-founder of Path2RAQA, which streamlines the regulatory affairs journey & got featured in Times Square for regulatory innovation. ... - Nov 24
... Skilled in FDA 510(k), ISO 13485, EU MDR, and PMS processes. Founder of an AI-powered compliance platform and Co-founder of Path2RAQA, which streamlines the regulatory affairs journey & got featured in Times Square for regulatory innovation. ... - Nov 24
Supplier Quality Engineer global
Illinois
... and Assessment, ASQC Communicative Manager Course En 46001, GMP, and FDA training course Continuous Improvement of process course Problem Solving training workshop course Design of experiment APQP, PPAP, FMEA, DOE, and PFMEA courses and training. ... - Nov 24
... and Assessment, ASQC Communicative Manager Course En 46001, GMP, and FDA training course Continuous Improvement of process course Problem Solving training workshop course Design of experiment APQP, PPAP, FMEA, DOE, and PFMEA courses and training. ... - Nov 24