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Milwaukee, WI, 53223
... reports • Managed and investigated product complaints, inquiries and product return issues • Provided interpretation of FDA regulatory guidance documents, regulations or directives which impacted the company • Interacted with domestic and ...
- 2011 Jan 03
Milwaukee, WI, 53223
Jim Shorer **** **** ******* ****** (***) *** - *823 Brown Deer, WI 53223 abkgoo@r.postjobfree.com OBJECTIVE Direct activities to produce pharmaceutical products that are FDA compliant, the most cost effective to the organization, and creates a safe ...
- 2010 Oct 01
Milwaukee, WI, 53218
... Maintained equipment and equipment records to FDA ISO 2000 and European Union standards. . Developed and implemented a preventative maintenance plan for building resulting in accurate records and reduced failures in services. . Refined quality ...
- 2010 Sep 22
Hartford, WI, 53027
... Brady, Rexford Papers and Rockwell Automation HAZLETON LABORATORIES (now COVANCE) - Madison, WI 1991 to 1994 Biomedical testing facility that offered testing services for meeting USDA, EPA and FDA approval, quality, and labeling requirements. PC ...
- 2010 Sep 15
Mequon, WI, 53097
... Monitored product development to ensure products complied with FDA regulations and U.S. market requirements. National Sales and Marketing Manager, 1997 to 1998 Created and hired direct sales force. Developed and implemented U.S. marketing and ...
- 2010 Sep 09
Thiensville, WI, 53092
... Worked on designing and creating reports of drug trials data for the Food and Drug Administration (FDA). . Deigned, coded, tested, implemented, documented applications (using Visual Basic and MS Access). . Collected and cleansed drug trials data and ...
- 2010 Sep 07
Milwaukee, WI, 53223
... Consulted with Wisconsin FDA to implement tamper proof packaging and labeling requirements to meet all regulations for retail market. Worked with personnel at Custom Cuts to implement new procedures and to meet all customer demand for products. ...
- 2010 Aug 26
Thiensville, WI, 53092
... Developed Functional Requirements Documentation for FDA eCTD (Electronic Common Technical Document) application . Developed User Requirements Document for Drug Application submission process. . Assisted in Validation of the system for release. . ...
- 2010 Apr 10
Menomonee Falls, WI, 53051
... Primary FDA (GMP) Supplier auditor. Managed staff of 6 and $75M budget. . Created and managed formal Minority Business Plan, improving Minority contracts by 95% to $1.1M. . Delivered over $1.5 M worth of cost savings via a deliberate program of ...
- 2010 Mar 09
Sussex, WI, 53089
... Followed the process for FDA and federal HIPAA regulations for protected patient information (PHI) and followed Agile Methodology / Scrum Development practices . Worked as an Architect in re-implementing the product with the latest technologies and ...
- 2010 Mar 09