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Resumes 221 - 230 of 7125 |
Spring Grove, IL
... Production Supervisor 2004-2005 Responsible for cGMP and CAPA Participated and lead Kaizen events Developed a team-based workforce accountable for safety, quality, customer service, and cost improvement metrics Recommend and verify cGMP. Led ...
- May 20
Panama City Beach, FL
... - IT Software Validation according to ISO and FDA • • Support in Internal Audits and Gap Analysis performance • CAPA and Non – Compliance innovative resolution skills • Internal IT and Corporate Procurement • IT Subject Matter Expert (SME ...
- May 20
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, ...
- 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 ...
- May 19
Chicago, IL
... Corrective Actions & Process Improvement: CAPA investigations and corrective actions, Troubleshooting and process improvements. Safety & Standards Compliance: OSHA and FDA safety standards, Harmonizing test methods, Training seminars on quality ...
- May 19
Hayward, CA
... QA Lead for internal audit of GMP Manufacturing, Quality Management Systems (training, document management, Investigations, Change Controls and CAPA) and other Quality Approve Chain of Custody documents for Investigational Cellular Therapy material ...
- May 18
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 ...
- May 17
Port Hueneme, CA
... Led Corrective and Preventive Action (CAPA) and risk analysis activities involved with technical support team. Led R&D and customer support teams specializing in the production of high-precision lathes used to manufacture contact and interocular ...
- May 16
Atlanta, GA
... Manage nonconformance reports and corrective and preventive action (CAPA) processes. Coordinate with cross-functional teams to ensure quality standards are met in production, supply chain, and product development. Prepare and present quality ...
- May 16
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 ...
- May 16