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Resumes 71 - 80 of 107 |
KCMO, MO
... Developed plan for retaining sales representatives and increasing sales of current products after receiving a not approvable FDA letter on a new product, resulting in the retention of all district sales representatives and increased sales to number ...
- 2012 Oct 02
Olathe, KS
... Responsible for compliance with OSHA, CLIA, CAP and FDA guidelines. Assures a safe and clean working environment and follows all instrument cleaning protocols. Performs and schedules complete routine semen analysis and provides patient notification ...
- 2012 Sep 25
KCMO, MO, 64157
... • Member of the Audit Team including internal audits and all ISO 9000 registration and FDA audits. DOCUMENT CONTROL COORDINATOR 03/1997 – 03/1999 Biotest Laboratories, Inc. Coon Rapids, MN • Maintained the documentation department through the ...
- 2012 Aug 09
Blue Springs, MO, 64015
... Ensure compliance: ISO 9001:2008, FDA 21CFR820 Medical Device Compliance, and NSF – 49 National Science Foundation, FM - Factory Mutual and ETL – Electrical Testing Laboratory requirements. 1997 - 2001 Quality Assurance Manager / Human Resources ...
- 2012 May 29
KCMO, MO, 64109
... PC Programs PROFESSIONAL EXPERIENCE Regulatory Chemist, The United States Food and Drug Administration (FDA), Lenexa, Kansas, 2002-2010 Conducted scientific analyses and tested broad range of food samples to detect pesticides and mycotoxin residue. ...
- 2012 Apr 19
Kansas City, MO, 64152
... Demonstrated ability to understand regulatory and compliance issues and designing and implementing facility operation plans that comply with FDA, UK and EU regulations Proven experience in the training of project teams and knowledge transfer. ...
- 2012 Apr 04
Prairie Village, KS, 66208
... RESEARCH & DEVELOPMENT SCHWAN’S SALES ENTERPRISES SALINA, KS January 1995 – December1997 Interpreted USDA & FDA regulations of the NLEA (Nutrition Labeling & Education Act) to develop accurate nutrition profiles for various frozen food products. ...
- 2011 Aug 29
De Soto, KS, 66018
... Clinical Training Clinical trials phases, processes FDA and ICH guidelines, including Good Clinical Practices (ICH-E6) Data cleaning procedures including query/DCF resolution and external vendor data reconciliation Electronic data capture systems ...
- 2011 Jul 26
Kansas City, MO, 64151
... Monitored BIS, CBP, FCC, FDA, and APHIS websites for regulation updates and changes and facilitated changes to procedures and work instructions to maintain compliance ? Assigned HTS and EAR classifications to a wide variety of electronic parts and ...
- 2011 Jul 26
Kansas City, MO, 64154
... branding campaigns on national, regional, state and local levels • Utilized WAN settings and SharePoint interfaces to enforce FDA Regulations and branding requirements • Increased client satisfaction through written and verbal communications • ...
- 2011 Mar 14