| Distance: | Resume alert | Resumes 241 - 250 of 25469 |
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
Data Entry Sales Associate
Johnstown, PA
... data into tables/graphs for upper management review •Retrieved documents from other departments •Adhered to company SOPs and FDA guidelines •Performed viable surface monitoring Biological Manufacturing Technician, Wyeth Vaccines, Marietta, PA ... - Jun 16
... data into tables/graphs for upper management review •Retrieved documents from other departments •Adhered to company SOPs and FDA guidelines •Performed viable surface monitoring Biological Manufacturing Technician, Wyeth Vaccines, Marietta, PA ... - Jun 16
General Manager Workplace
Cayuga, NY
... • Directed safety operations and maintained clean work environment to adhere to FDA and OSHA requirements. • Developed and implemented operational strategies to improve efficiency, reduce costs, and maximize customer satisfaction. • Used strong ... - Jun 16
... • Directed safety operations and maintained clean work environment to adhere to FDA and OSHA requirements. • Developed and implemented operational strategies to improve efficiency, reduce costs, and maximize customer satisfaction. • Used strong ... - Jun 16
Clinical Trial Regulatory Compliance
Chicago, IL
... Expert in regulatory compliance and clinical documentation, ensuring strict adherence to ICH-GCP, FDA, HIPAA, and IRB protocols, implementing risk-based monitoring and audit readiness strategies, resulting in 100% regulatory compliance and zero ... - Jun 16
... Expert in regulatory compliance and clinical documentation, ensuring strict adherence to ICH-GCP, FDA, HIPAA, and IRB protocols, implementing risk-based monitoring and audit readiness strategies, resulting in 100% regulatory compliance and zero ... - Jun 16