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Resumes 51 - 60 of 79 |
Citrus Heights, CA
... 1994) Maintained documents pertaining to procurement, manufacturing and testing of MRI equipment for ISO9001 and FDA certification which included bill of materials, design drawings, specifications, S/W code, printed circuit board documents, ...
- 2014 Feb 26
Elk Grove, CA
... S umma ry of Knowledge and Experience I have full understanding of complying with FDA Regulations, ICH Guidelines and following GCP Standards and H IPAA. My experience has provided me with the opportuni ty to use and work with multiple medical ...
- 2013 Nov 29
Roseville, CA
... Knowledge of cGMP, ISO, ICH and FDA guidelines. Excellent communication skills (verbal and written), analytical and problem solving skills. Worked in small and mid-sized teams and demonstrated effective team player and organizer abilities. Education ...
- 2013 Jul 10
Galt, CA
... Skill Set Excel/Word/Power Point FDA/ISO/SOX Guidelines Supplier Sourcing/Qualification/Evaluation/Management SAP/LN ERP Systems Contract Negotiation/Development Market Trend Analysis Commodity Pricing Agreement QA/QC Process & Procedures AMAPS/SBT ...
- 2013 Mar 27
Sacramento, CA
... Critical thinker Certified Forklift Operator Vast HVAC knowledge Initiative to work independently Strong background in FDA drug safety guidelines Excellent telephone etiquette Pharmaceutical storage awareness Customer- and service-oriented Loss ...
- 2012 Dec 12
Davis, CA
... (N 29) Characteristic Huang) and caffeine reported similar weight loss findings.7,8 The US Food and Drug Administration (FDA) banned the sale Race or ethnic group African American 1 2 of dietary supplements containing ephedrine alkaloids in ...
- 2012 Nov 09
Sacramento, CA
... scheduled examination appointments for US Customs, USDA, and FDA; maintained/updated customer files; copying; faxing; filing; handled telephone contacts with customers and others outside of the organization; handled daily will call customers and ...
- 2012 Oct 03
Sacramento, CA
... investigated, and reported findings of product quality investigations for clinical products according to GMP and FDA regulations • Compiled and tracked trending reports and periodic summary reports on product quality findings • Maintained ...
- 2012 Apr 29
Sacramento, CA
... Knowledgeable in FDA, IRB, ICH, GCP and HIPPA requirements. Extensive experience providing a full range of regulatory documentation management services for clinical trials. A versatile professional that works effectively either independently or as a ...
- 2011 Jun 23
Sacramento, CA, 95817
... Control Inspector Lead •Preformed lot inspections and first article inspections on incoming raw material, parts and subassemblies for various coronary catheter and coronary catheter related product line to ISO 13485: 2003, FDA and GMP standards. ...
- 2011 Jun 12