| Distance: | Resume alert | Resumes 161 - 170 of 25468 |
Administrative Assistant Data Entry
Oak Park, IL, 60302
... Maintained product quality and safety by making sure that GMP (Good Manufacturing Practices), FDA and other regulatory requirements were followed. . Reviewed SOPs, quality documentation, and batch records were examined and approved to guarantee ... - Jun 25
... Maintained product quality and safety by making sure that GMP (Good Manufacturing Practices), FDA and other regulatory requirements were followed. . Reviewed SOPs, quality documentation, and batch records were examined and approved to guarantee ... - Jun 25
Customer Service Emergency Medical
Baton Rouge, LA
CHRISTA RUSSO CERTIFICATIONS FDA Certified in Human Drug Review & Approval Basics • NIDA Certified in Good Clinical Practice • Certified with the Mayo Clinic in Category A, Infectious Substance Affecting Humans & Category B, Biological Substance ... - Jun 25
CHRISTA RUSSO CERTIFICATIONS FDA Certified in Human Drug Review & Approval Basics • NIDA Certified in Good Clinical Practice • Certified with the Mayo Clinic in Category A, Infectious Substance Affecting Humans & Category B, Biological Substance ... - Jun 25
Clinical Testing Manager
Washington, DC, 20017
... **** **** ****** ** Washington DC 20017 Email: *********@*****.*** Phone: 304-***-**** Summary Extensive work experience in GCLP, GLP, GMP and FDA regulated laboratories 19 years of laboratory experience, including in-house developed ELISAs, ... - Jun 25
... **** **** ****** ** Washington DC 20017 Email: *********@*****.*** Phone: 304-***-**** Summary Extensive work experience in GCLP, GLP, GMP and FDA regulated laboratories 19 years of laboratory experience, including in-house developed ELISAs, ... - Jun 25
Pharmacy Technician Clinical Research
Marietta, GA
... company processes and procedures, and in compliance with GCP, ICH, HIPAA, FDA, USP 797, USP 800, state Boards of Pharmacy, and company SOPs: Coordinating and advising site staff on drug distribution services for investigational medications. ... - Jun 25
... company processes and procedures, and in compliance with GCP, ICH, HIPAA, FDA, USP 797, USP 800, state Boards of Pharmacy, and company SOPs: Coordinating and advising site staff on drug distribution services for investigational medications. ... - Jun 25
Senior Buyer Accounts Payable
Crestline, OH, 44827
... ●FDA regulations and ISO 13485. PROFESSIONAL EXPERIENCE ZIMMER BIOMET, Remote Feb 2023 - Jun 2025 Senior Buyer ●Engineering/Quality coordination on spec conformance and non-conformance resolution ●Raw materials and contract manufactured finished ... - Jun 25
... ●FDA regulations and ISO 13485. PROFESSIONAL EXPERIENCE ZIMMER BIOMET, Remote Feb 2023 - Jun 2025 Senior Buyer ●Engineering/Quality coordination on spec conformance and non-conformance resolution ●Raw materials and contract manufactured finished ... - Jun 25
IT Project Manager
Alabaster, AL
... (currently in progress) Technical Skills Project Management Tools: Jira, Clarity/NIKU, Microsoft Project Manager Documentation & Analysis: Microsoft Office Suite & Google Docs Methodologies: Agile, Scrum, Waterfall, PMBOK Compliance: SOX, HIPAA, FDA - Jun 25
... (currently in progress) Technical Skills Project Management Tools: Jira, Clarity/NIKU, Microsoft Project Manager Documentation & Analysis: Microsoft Office Suite & Google Docs Methodologies: Agile, Scrum, Waterfall, PMBOK Compliance: SOX, HIPAA, FDA - Jun 25
Medical Devices Risk Management
Henderson, NV
... Biocompatibility / Toxicology Risk Assessment Subject Matter Expert (SME), ISO 10993-1:2018 Biocompatibility / Toxicology, EU MDR 2017/745 Regulation on Medical Devices, EU MDR remediation, FDA regulations (21 CFR 820), CAPA, Gap Analysis, and FDA ... - Jun 24
... Biocompatibility / Toxicology Risk Assessment Subject Matter Expert (SME), ISO 10993-1:2018 Biocompatibility / Toxicology, EU MDR 2017/745 Regulation on Medical Devices, EU MDR remediation, FDA regulations (21 CFR 820), CAPA, Gap Analysis, and FDA ... - Jun 24
Center Manager Customer Service
Atlanta, GA
... ● Dedicated Components Specialist with 10+ years of experience working in an FDA regulated environment to prepare blood components meant for transfusion. I specialize in the safe handling and processing of blood components with consistency and ... - Jun 24
... ● Dedicated Components Specialist with 10+ years of experience working in an FDA regulated environment to prepare blood components meant for transfusion. I specialize in the safe handling and processing of blood components with consistency and ... - Jun 24
Quality Control Regulatory Compliance
Charlotte, NC, 28217
... Experience in CGMP, GLP, FDA regulated environment and follows GDP. Empower to initiate and process data. HPLC and GC setup, troubleshooting and basic maintenance. Perform timely & accurate quality control analysis using test established. Perform ... - Jun 24
... Experience in CGMP, GLP, FDA regulated environment and follows GDP. Empower to initiate and process data. HPLC and GC setup, troubleshooting and basic maintenance. Perform timely & accurate quality control analysis using test established. Perform ... - Jun 24
Business Analyst Product Development
Satellite Beach, FL
... Supplier Data Steward – traceability, reconciliation of global supplier throughout the PLM and business ●Johnson & Johnson: Pharma/Data Migration oContributor and PM on migrating medical device and pharma data from FDA to EUDAMED, GUDID, etc. ... - Jun 24
... Supplier Data Steward – traceability, reconciliation of global supplier throughout the PLM and business ●Johnson & Johnson: Pharma/Data Migration oContributor and PM on migrating medical device and pharma data from FDA to EUDAMED, GUDID, etc. ... - Jun 24