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Resumes 431 - 440 of 7109 |
Stone Mountain, GA
... Quality Systems, CAPA, Change Control, Document Control, audits and deviations in FDA, OSHA, EPD, EPA and cGMP regulated environments. Excellent written and oral communication skills. Career History Quality Assurance Associate ISS Intl., for Takeda, ...
- 2025 May 19
Aberdeen, MD
... I am skilled in risk assessment, corrective and preventive actions (CAPA), planned and unplanned deviations and regulatory compliance with FDA, ISO, and GMP standards. Passionate about learning and applying cybersecurity principles to safeguard ...
- 2025 May 19
Red Lion, PA
... I lead the oversight of regulatory files, submissions, and documentation, while also coordinating internal audits and scheduling, facilitator for CAPA coordination and completion, and document control administration. Working cross-functionally and ...
- 2025 May 17
Martville, NY, 13111
... Executes CAPA, Failure Investigations / Corrections of design related quality issues. tes in PPL - Post Product Launch failure investigations. Directly support design change control activities with Suppliers / External Manufacturers. Review and ...
- 2025 May 16
Owens Cross Roads, AL
... Provided environmental program management for HAZCOM, RPP (Respiratory Protection Program, Laser/Radiation Protection Program, CAPA management, permit compliance, and sustainability. Utilized environmental management software platforms e.g. DOEHRS, ...
- 2025 May 15
Baltimore, MD
... Provided support for corrective and preventive action (CAPA) plans to improve laboratory efficiency and accuracy. SQL, Python, R, Tableau (FDA, ICH, GCP, GMP) (HPLC, UV-Vis Spectroscopy, FTIR, NMR) Epic/EHR, Medical Coding, HIPAA Compliance ...
- 2025 May 15
Fremont, CA
... ●Worked in a variety of Computer System Validation Projects: ●Labware LIMS (Laboratory Information Management System), ●Watson LIMS, ●Clinical Trial Management System (CTMS), ●Veeva Vault (QDocs, QMS), ●Track Wise (CAPA, Change Control Management ...
- 2025 May 15
Hillsborough, NJ
... Quality Management Configuration and related Software Validation Deliverables Include: ●Corrective and Preventative Action (CAPA) System ●Customer Complaint and Field Alert Reporting System ●Out of Specification (OOS) Quality Control Investigations ...
- 2025 May 15
Oakland, NJ
... SKILLS EXPERIENCE Lead Auditor ISO 13485/EN ISO 13485 FDA 21 CFR MDSAP IVD/IDVR MDD/MDR CAPA, Complaint, PMS Associate Director, Clinical Quality Assurance – CERUS, CA 2021- 2024 Responsible for overseeing compliance processes within the Clinical ...
- 2025 May 15
Claymont, DE
... of study tasks and teams(s) • Attends relevant meetings for sponsor-related activities, cooperative groups and the organization’s staff meetings • Assists with CAPA and training related to research compliance, quality control, and quality assurance. ...
- 2025 May 14