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Resume alert |
Resumes 21 - 30 of 42 |
Centereach, NY
... PA Sr QA/Validation Analyst xmLabeling/GLS(ABBVIE) May 14 to Till Date XmLabeling is a Product based global content Management system that addresses all FDA US Submissions, QRD EMEA Submissions and Clinical Labeling of World Wide Pharma Clients . ...
- 2015 Jun 19
Selden, NY
... Provided documentation assistance to scientists in the correct preparation of technical documents for submissions to the FDA and other Health Authorities. Responsible for new employee education and problem resolution for using the company ...
- 2015 Apr 16
East Patchogue, NY
... * Established compliance with corporate procedures and audits to FDA 820, Canadian & MDD, Japan (PAL) & China regulations * Responsible for full launching of new products from conception through design and development to corporate compliance ...
- 2015 Jan 21
Port Jefferson Station, NY
... Making sure that all activities are in compliance with FDA and state rules and regulations. • Working in teams and shifts to ensure continuous production of baked and frozen bread goods. In charge of weekly sanitizing and cleaning of all machinery. ...
- 2014 Dec 15
Coram, NY
... and handling high volume of internal and external communications, to include email, mail, and phone calls - Leverage technical skill in publishing Food and Drug Administration (FDA) regulated documents to a shared point location on the company’s ...
- 2014 Oct 20
Rocky Point, NY
... Was responsible to inform FDA for every procedure made Clinical Research Coordinator, Intec Pharma Ltd., Jerusalem, Israel, October 2010 - May 2011 Start-up Drug development Company . Managed protocol between patients with Parkinson's disease, ...
- 2014 Jun 20
Holtsville, NY
... and Johnson Ortho Clinical Diagnostics, Raritan, NJ 6/2009 – 12/2009 SAS Programmer (Consultant) Environment: Base SAS, SAS/Macro, SQL Responsibilities: Generated required tables, listings and graphs from clinical trial data for FDA submissions. ...
- 2014 Feb 04
Holbrook, NY
... Assisted physicians and researchers to document and submit patient adverse events to the IRB, and FDA . Reviewed and approved quality systems documents to determine compliance with regulatory regulations and standards . Responsible for submitting ...
- 2013 May 15
Mastic Beach, NY
... Marine Corps, US Coast Guard, National Park Service, FDA, HUD, NYCTA, MTA Bridges & Tunnels, NYC DDC, and NYC Parks. Historic Restoration Specialists for Heritage and Sacred Sites Page 1 Primary Trades Stonemasonry, carpentry, project management, ...
- 2012 Nov 20
Riverhead, NY
... and write reports for complex problems Serve as a liaison with Process Development Assist with design May interact with FDA inspectors Initiate and investigated NCs and CAPA implementation Change Control Owner Promote a healthy work environment ...
- 2012 Nov 19