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Resume alert |
Resumes 51 - 60 of 119 |
Greensboro, NC
... cGMP/FDA upgrade of existing morphine/codeine production facility Osram/Sylvania - Central Falls, Rhode Island New frost line fume exhaust system installation for HCF used in frosting light bulbs. Included coated ductwork and exhaust to a primary ...
- 2014 Oct 23
Greensboro, NC
... Responsible for monitoring and maintaining the equipment in a fast paced work environment while complying to FDA and GMP guidelines set for a clean room manufacturing environment. 1988-1993 Furniture Industry, Martinsville, VA. Bassett Furniture ...
- 2014 Jun 28
Stokesdale, NC
... Participated in FDA audits and resolution of CAPA . Manage non-conformance issues, corrective actions and developed action plans . Highly detail oriented, strong interpersonal skills, attentive to company needs handling sensitive situations in a ...
- 2014 Jun 24
Trinity, NC
... Familiar with Electronic submission guidelines to FDA • Extensive experience with concatenating, interleaving, merging, sorting, printing and reporting data in M S Excel and R TF format. • Strong expertise in SAS Base procedures, Reporting and ...
- 2014 May 20
Randleman, NC
... participate in Regulatory, FDA and customer on-site audits; create/modify existing SOP and Work Instructions as needed. Completed Red Belt training and participated on Green Belt team to increase proficiency in investigating deviations and ...
- 2014 May 04
Jamestown, NC
... Liaison and led in all customer audits to ISO, FDA and cGMP standards; Led teams in implementing a 5S program in their departments; Re-implement the Safety Committee, safety inspections and tracking of near-miss, recordable and lost time accidents. ...
- 2014 Apr 18
Colfax, NC, 27235
... Automotive, Security, Engineering, Medical Devices, Consumer (B-to-B, B-to-C), 3PL, Retail, Entertainment, Finance, Technology, Regulatory compliance (FDA, FTC, HIPPA, SOX), Six Sigma, Lean principles PROFESSIONAL EMPLOYMENT NEWBREED Logistics, Inc. ...
- 2014 Mar 28
Winston Salem, NC
... • Took vital signs at study enrollment and throughout the study per protocol • Monitored subjects after dosing and did various other duties as needed • Maintained thorough familiarity and compliance with state and federal regulations and FDA ...
- 2014 Mar 19
High Point, NC
... Location Date SAP I nformation Consultant Technology Mentor, Puerto Rico Nov 2013 – present • SAP Consultant – I PR (Astrazeneca, FDA regulated organization) o SAP Validation remediation solution assessment for SAP Latin America (LATAM) sites Change ...
- 2014 Mar 17
Asheboro, NC
... • January 2008 – January 2011 Mendenhall Clinical Research Center – High Point, NC Phlebotomist/ Lab Tech Over 100 draws per day for clinical trials for FDA approved drug studies. Comprehensive • draws for some studies-multiple tube draws up to 30 ...
- 2013 Dec 02