| Resume alert | Resumes 61 - 70 of 6814 |
R D Validation Engineer
Lake Forest, CA, 92630
... • Performing CAPA investigations. • Defining and planning budgets, schedules, and resources for manufacturing operations. • Knowledge in ISO-11070, ISO-9001, ISO-13485, and FDA 510k guidelines. Location: • Lake Forest, CA 92630 Current job search ... - Mar 30
... • Performing CAPA investigations. • Defining and planning budgets, schedules, and resources for manufacturing operations. • Knowledge in ISO-11070, ISO-9001, ISO-13485, and FDA 510k guidelines. Location: • Lake Forest, CA 92630 Current job search ... - Mar 30
Supply Chain Clinical Trials
Monmouth Junction, NJ
... Conducted data analysis and identified trends in non-conformances for the investigative phase of CAPA (Corrective Action Preventative Action). Executed and improved metric for on time shipments (100%). Strategy included tracking sheet to monitor all ... - Mar 29
... Conducted data analysis and identified trends in non-conformances for the investigative phase of CAPA (Corrective Action Preventative Action). Executed and improved metric for on time shipments (100%). Strategy included tracking sheet to monitor all ... - Mar 29
Quality Control Project Management
Derby, City of Derby, DE1 3FJ, United Kingdom
... Developed Site level CAPA system in compliance with FDA 21 CFR 820 QSR’s (cGMP) for Class I and Class II medical devices, including DMR, DHR management. Managed, Administered CAPA's (Corrective and Preventive Actions) -Lead and guide to assure ... - Mar 29
... Developed Site level CAPA system in compliance with FDA 21 CFR 820 QSR’s (cGMP) for Class I and Class II medical devices, including DMR, DHR management. Managed, Administered CAPA's (Corrective and Preventive Actions) -Lead and guide to assure ... - Mar 29
Quality Control
Dayton, NJ, 08810
... ● Document handling (i.e Change Control, Deviation, CAPA, OOS,OOT,STP, Planned Deviation, Product Complain etc..) ● Participate in Documentation Closing process after the investigation is done. ● Verify raw material and components prior to usage as ... - Mar 29
... ● Document handling (i.e Change Control, Deviation, CAPA, OOS,OOT,STP, Planned Deviation, Product Complain etc..) ● Participate in Documentation Closing process after the investigation is done. ● Verify raw material and components prior to usage as ... - Mar 29
Drug Safety Information Technology
Belle Mead, NJ
... • CAPA Lead for IPOS systems, provide expertise to author QE and suggest adequate corrective/preventive measures by systematic investigation and record root cause analysis of identified problems/risk preventing recurrence. • Business member for ... - Mar 29
... • CAPA Lead for IPOS systems, provide expertise to author QE and suggest adequate corrective/preventive measures by systematic investigation and record root cause analysis of identified problems/risk preventing recurrence. • Business member for ... - Mar 29
Business Analyst Change Management
Iselin, NJ, 07067
... Involved in supporting the CAPA implementation steps. Knowledge of QUMAS Doc Compliance, medical device quality management system (QMS) a regulatory content management for electronic control of all documentation and QUMAS Process Compliance, a ... - Mar 28
... Involved in supporting the CAPA implementation steps. Knowledge of QUMAS Doc Compliance, medical device quality management system (QMS) a regulatory content management for electronic control of all documentation and QUMAS Process Compliance, a ... - Mar 28
Quality Engineer Supplier
Bluffton, SC
... Fault Tree Analysis, CAPA) for test failures. Developed improved methods of managing validation and contract requirements communication to supply chain that resulted in 40% reduction in contract errors. Supplier Quality Engineering and Operations ... - Mar 28
... Fault Tree Analysis, CAPA) for test failures. Developed improved methods of managing validation and contract requirements communication to supply chain that resulted in 40% reduction in contract errors. Supplier Quality Engineering and Operations ... - Mar 28
Quality Control Raw Materials
Philadelphia, PA
... Identified CAPA and responsible for ensuring that the findings/improvements were made through Change Control. BAXTER HEALTHCARE CORPORATION, Cherry Hill, New Jersey 2002-2007 Manager I, Analytical Research and Development Led seven-member team to ... - Mar 28
... Identified CAPA and responsible for ensuring that the findings/improvements were made through Change Control. BAXTER HEALTHCARE CORPORATION, Cherry Hill, New Jersey 2002-2007 Manager I, Analytical Research and Development Led seven-member team to ... - Mar 28
Quality Assurance Senior Manager
Nashik, Maharashtra, India
... Demonstrated knowledge of techniques customarily acquired by hands on experience in applying advanced knowledge of FMEA, PPAP, MSA, SPC, APQP, Control Plan, RCA, 7QC Tools, 5’S, Error Proofing, CAPA, SOP.Planning and control principles and ... - Mar 28
... Demonstrated knowledge of techniques customarily acquired by hands on experience in applying advanced knowledge of FMEA, PPAP, MSA, SPC, APQP, Control Plan, RCA, 7QC Tools, 5’S, Error Proofing, CAPA, SOP.Planning and control principles and ... - Mar 28
Drug Safety Data Management
Thousand Oaks, CA, 91362
... Drafting errors across site gathering RCAs, implementing and closing CAPA on time, monitoring Turn Around Time (TAT) for ICSRs submission, and handling the triage of reports for daily workflow management. • Ad hoc activity EV Triage. •Involving in ... - Mar 27
... Drafting errors across site gathering RCAs, implementing and closing CAPA on time, monitoring Turn Around Time (TAT) for ICSRs submission, and handling the triage of reports for daily workflow management. • Ad hoc activity EV Triage. •Involving in ... - Mar 27