| Distance: | Resume alert | Resumes 331 - 340 of 7109 |
Medical Device Risk Management
Hackensack, NJ
... -Managed the CAPA program. Generated, monitored and ensured effective implementation of improved processes. -Developed course materials and trained employees on the Quality Management System ISO, 21 CFR Part 820 and audit preparation. -Reviewed all ... - 2025 Jun 27
... -Managed the CAPA program. Generated, monitored and ensured effective implementation of improved processes. -Developed course materials and trained employees on the Quality Management System ISO, 21 CFR Part 820 and audit preparation. -Reviewed all ... - 2025 Jun 27
Program Manager Data Architect
Broomall, PA
... Incident investigations, CAPA and Action item creation. ●Permitting and OSHA recordkeeping as required. Work with external agencies to maintain compliance across all local, State and Federal guidelines. ●EHS data management (Gensuite) and data ... - 2025 Jun 26
... Incident investigations, CAPA and Action item creation. ●Permitting and OSHA recordkeeping as required. Work with external agencies to maintain compliance across all local, State and Federal guidelines. ●EHS data management (Gensuite) and data ... - 2025 Jun 26
Quality Assurance Management
Greenville, SC
... • EU-GMP • Product Recall • Deviation Management • Quality Management • APQR/CPV • Risk Management • Validation /Qualification • Change Control • AQL • Internal Audit • Market Complaint • Cleaning Validation • Batch Release • CAPA, OOS/OOT • ... - 2025 Jun 26
... • EU-GMP • Product Recall • Deviation Management • Quality Management • APQR/CPV • Risk Management • Validation /Qualification • Change Control • AQL • Internal Audit • Market Complaint • Cleaning Validation • Batch Release • CAPA, OOS/OOT • ... - 2025 Jun 26
Quality Assurance Engineer
Gaborone, Botswana
... oContinual Improvement: Utilized root cause analysis (RCA) and CAPA strategies to manage quality issues, ensuring all testing processes met or exceeded quality benchmarks. SENIOR TECHNICAL OFFICER / CHEMIST Reporting to the Manager - Chemical and ... - 2025 Jun 26
... oContinual Improvement: Utilized root cause analysis (RCA) and CAPA strategies to manage quality issues, ensuring all testing processes met or exceeded quality benchmarks. SENIOR TECHNICAL OFFICER / CHEMIST Reporting to the Manager - Chemical and ... - 2025 Jun 26
Supply Chain Stand-Up Forklift
Louisville, KY, 40214
... to improve Process (SPC) Continuous Improvement, Purchasing Materials Management, Demand Planning, Warehouse Operations, Lean Manufacturing, Continuous Improvement, 5S, Six Sigma, Root Cause Analysis, Corrective and Preventive Action (CAPA) - 2025 Jun 26
... to improve Process (SPC) Continuous Improvement, Purchasing Materials Management, Demand Planning, Warehouse Operations, Lean Manufacturing, Continuous Improvement, 5S, Six Sigma, Root Cause Analysis, Corrective and Preventive Action (CAPA) - 2025 Jun 26
Quality Control Regulatory Compliance
Deep River, CT
... Coordinated with the QA department to address OOS (Out-of-Specification) results, CAPA implementation, and audit readiness. Monitored environmental conditions and performed cleaning verification to maintain regulatory compliance within lab settings. ... - 2025 Jun 25
... Coordinated with the QA department to address OOS (Out-of-Specification) results, CAPA implementation, and audit readiness. Monitored environmental conditions and performed cleaning verification to maintain regulatory compliance within lab settings. ... - 2025 Jun 25
Quality Management Operations
Houston, TX, 77002
... Leader of Non-Conformities Report System and CAPA System. Leader of NPS and NCM Processes Integration. Responsible of leading the Global Library Maintenance, processes mapping, document control including products specifications and quality records. ... - 2025 Jun 25
... Leader of Non-Conformities Report System and CAPA System. Leader of NPS and NCM Processes Integration. Responsible of leading the Global Library Maintenance, processes mapping, document control including products specifications and quality records. ... - 2025 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 ... - 2025 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 ... - 2025 Jun 24
Quality Specialist
East Greenville, PA
... John Blue East Greenville PA Phone #: 610-***-**** Linkedin: www.linkedin.com/in/john -blue-03b385198 CORE EXPERTISE • Quality Management • Quality Improvement • Writing Deviations • Technical Writing • Investigations/CAPA/ Root Cause Analysis • ... - 2025 Jun 24
... John Blue East Greenville PA Phone #: 610-***-**** Linkedin: www.linkedin.com/in/john -blue-03b385198 CORE EXPERTISE • Quality Management • Quality Improvement • Writing Deviations • Technical Writing • Investigations/CAPA/ Root Cause Analysis • ... - 2025 Jun 24
Operations Management Asset
New Delhi, Delhi, India
... Ensuring implementation of CAPA, de-bottlenecking in process, spares indigenization, engineering solutions, in place of admin. Control. Conducting Root Cause analysis and FMEAs to identify mitigation/corrective actions. Asset Management to maximize ... - 2025 Jun 24
... Ensuring implementation of CAPA, de-bottlenecking in process, spares indigenization, engineering solutions, in place of admin. Control. Conducting Root Cause analysis and FMEAs to identify mitigation/corrective actions. Asset Management to maximize ... - 2025 Jun 24