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Resumes 31 - 40 of 51 |
San Jose, CA, 95123
... Assisted QA and Compliance department with QA audits of clinical database, client and FDA audits of the company. Central Files Associate (2000-2004) . Processed visit reports submitted to Central Files for multiple Pharmaceutical clinical trials. . ...
- 2011 Jul 24
San Jose, CA, 95138
... Prepared certificates such as FDA certificates, NAFTA Certificates of Origin, certificate of Free Sale and others. Submitted Bill of Lading instructions, Insurance certificate, shipment manifest, Foreign brokers/agents' pre-alert including ...
- 2011 Jul 03
San Jose, CA, 95120
... Manage quality processes in accordance with Food and Drug Administration (FDA) guideline. . Coordinate lab activities with Firmware, Hardware, and Software Development teams. . Communicate test status, progress, problems and changes to functional ...
- 2011 Jun 21
San Jose, CA, 95123
... Provided assistance with the preparation for client and FDA audits of Clinimetrics . Prepared and performed QA audits of clinical data . Assisted QA/Compliance Department with query resolutions . Provided support with the maintenance, distribution, ...
- 2011 Jun 01
Salinas, CA, 93906
... Training customers in proper usage of several types of equipment and validating equipment for FDA compliance. . On-site troubleshooting, analysis and maintenance of several types of equipment. . Self-supervising - responsible for arranging own ...
- 2011 Feb 22
Gilroy, CA, 95020
... - IT Member of the site Validation Review Board ensuring systems and process compliance with the Validation Master Plan, FDA regulations, and Corporate guidelines. - Leader of the 2003 Team of the Year (Validation & Upgrade of National Field Service ...
- 2010 Oct 29
San Jose, CA, 95123
... Successfully completion of cross-functional project teams implementation of policies and procedures that ensure adherence to QSR, ISO, DEA, FDA, DOT, IATA and other business regulations. . Expert understanding of Microsoft operating systems ...
- 2010 Oct 19
Los Gatos, CA, 95033
... Experienced writing for a FDA regulated audience . Expert FrameMaker and Acrobat user . Strong knowledge of ISO 9000, CGMP, and Six Sigma. . Experience launching Technical Publication Departments Professional Experience Sr. Technical Writer Hospira, ...
- 2010 Sep 15
Salinas, CA, 93906
... recordkeeping of daily sanitizing procedures to comply with FDA’s requirements • Inspect and check all the incoming raw product to assure complies with quality standards • Perform Food Safety and Quality audits and head monthly food safety meeting. ...
- 2010 Aug 30
San Jose, CA, 95111
... basic laboratory tasks and provide QC support, ,lab cleaning, along with special assignments Experience working within FDA’s cGMP/QSRs, ISO 9000 Knowledge and experience with inspection tools: Calipers, Micrometers, Microscopes, Video scopes, ...
- 2010 Aug 27