| Distance: | Resume alert | Resumes 381 - 390 of 25511 |
Brand Strategist Financial Services
New York City, NY
... We also supported their FDA applications for 5 new products and developed brand systems for each, including strategy, names, logos and packaging. • Altegrity: Created Day 1 and continuing marketing, PR, website, creative and sales material for the ... - Jun 17
... We also supported their FDA applications for 5 new products and developed brand systems for each, including strategy, names, logos and packaging. • Altegrity: Created Day 1 and continuing marketing, PR, website, creative and sales material for the ... - Jun 17
Data Analyst Power Bi
Irvine, CA
... Skilled in data cleaning, statistical modeling, and visualization, with a strong background in regulatory-compliant data reporting (CDISC, FDA). Proven ability to automate data cleaning, design interactive dashboards and visualization reports, and ... - Jun 17
... Skilled in data cleaning, statistical modeling, and visualization, with a strong background in regulatory-compliant data reporting (CDISC, FDA). Proven ability to automate data cleaning, design interactive dashboards and visualization reports, and ... - Jun 17
Clinical Research Coordinator
Seattle, WA
... Medical Device (Engineering) Trials ● University, Hospital, Clinic & Community-Based Research ● Regulatory Compliance (GCP, ICH, FDA, IRB Submissions) ● Data Management (Medrio, Redcap, Oracle, EPIC, Florence) ● Participant Recruitment & Retention ... - Jun 17
... Medical Device (Engineering) Trials ● University, Hospital, Clinic & Community-Based Research ● Regulatory Compliance (GCP, ICH, FDA, IRB Submissions) ● Data Management (Medrio, Redcap, Oracle, EPIC, Florence) ● Participant Recruitment & Retention ... - Jun 17
Administrative Assistant Quality Control
Jersey City, NJ, 07302
... University of Chicago — Certificate in Clinical Trials Management and Regulatory Compliance 2024 – 2025 Training in GCP, FDA/ICH regulations, trial operations, budgeting, and oversight—preparing for roles in pharma or lab environments. University of ... - Jun 17
... University of Chicago — Certificate in Clinical Trials Management and Regulatory Compliance 2024 – 2025 Training in GCP, FDA/ICH regulations, trial operations, budgeting, and oversight—preparing for roles in pharma or lab environments. University of ... - Jun 17
Quality Assurance Control
Beaufort, SC
... • Troubleshooting and performing preventative maintenance • Quality Control - Compliance with Quality Assurance Requirements • FDA and USDA Compliance • OSHA Compliance • Supervise and train Production personnel, performance evaluations • Completed ... - Jun 17
... • Troubleshooting and performing preventative maintenance • Quality Control - Compliance with Quality Assurance Requirements • FDA and USDA Compliance • OSHA Compliance • Supervise and train Production personnel, performance evaluations • Completed ... - Jun 17
Quality Control Analyst Ii
Raleigh, NC
... Completed development classes including Deviations, Root Cause Analysis, and CAPA Resolution, FDA Audit Prep, Excel, 7 Habits Foundations, Writing Effective SOPs, Building at the Speed of Trust, among others. SME for function testing. Proficiency ... - Jun 17
... Completed development classes including Deviations, Root Cause Analysis, and CAPA Resolution, FDA Audit Prep, Excel, 7 Habits Foundations, Writing Effective SOPs, Building at the Speed of Trust, among others. SME for function testing. Proficiency ... - Jun 17
Continuous Improvement Puerto Rico
Fajardo
... Solid training and certification in cGMP and Industrial Validation covering IQ, OQ, and PQ Protocol Development, Risk Analysis, Disposition and Validation Documentation Processes to meet FDA requirements within the pharmaceutical, and biologic ... - Jun 17
... Solid training and certification in cGMP and Industrial Validation covering IQ, OQ, and PQ Protocol Development, Risk Analysis, Disposition and Validation Documentation Processes to meet FDA requirements within the pharmaceutical, and biologic ... - Jun 17
Operator of machine
Indianapolis, IN
... Abbott Laboratories, Westbrook, ME 12/2019 - 02/2021 Production Specialist Job Duties and Tasks • Operated production machinery to create test kit subassemblies • Followed production guidelines and SOPs for all FDA documentation • Worked in a ... - Jun 17
... Abbott Laboratories, Westbrook, ME 12/2019 - 02/2021 Production Specialist Job Duties and Tasks • Operated production machinery to create test kit subassemblies • Followed production guidelines and SOPs for all FDA documentation • Worked in a ... - Jun 17
Regulatory Affairs Product Development
Hyderabad, Telangana, India
... Regulatory support and guidance to product development team PIND review and submission to FDA. Review of Technical documents such as pharmaceutical Development Report, Batch Manufacturing Records, stability protocols, DMF, Risk assessment and all ... - Jun 16
... Regulatory support and guidance to product development team PIND review and submission to FDA. Review of Technical documents such as pharmaceutical Development Report, Batch Manufacturing Records, stability protocols, DMF, Risk assessment and all ... - Jun 16
Raw Materials Have Experience
Houston, TX
... Science Institute, Ahmedabad (India), April 1990 - FDA approved Chemist by Drugs Controller, Ahmedabad (India) Computer Knowledge & Skills: - Experience with ASTM and ACS methods for pure petrochemicals testing’s. - Experience with chemistry ... - Jun 16
... Science Institute, Ahmedabad (India), April 1990 - FDA approved Chemist by Drugs Controller, Ahmedabad (India) Computer Knowledge & Skills: - Experience with ASTM and ACS methods for pure petrochemicals testing’s. - Experience with chemistry ... - Jun 16