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Resume alert Resumes 51 - 60 of 4619

Production Manager Management System

San Jose, CA, 95123
... Work trajectory PLASCO MOLDING CLAYES Date of entry: November -2022 to December 2023 • Manage the execution of quality initiatives and corrective and preventive action (CAPA) across all manufacturing value streams to achieve strategic quality ... - Mar 30

Document Control Specialist

Santa Clara, CA
... In programs ●Verify hard copy e-records matched archival repository in Veeva Vault ●Verify the QMS requirements for archiving Deviations, CAPA, Change Control, Audits, Batch Records, Supply Chain reports aligned with Veeva Vault corporate standards. ... - Mar 30

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

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

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

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

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

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

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

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
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