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Glp resumes in Columbus, OH, 43215

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Chemist

Columbus, OH, 43228
... Good understanding of cGMP/GLP, ICH guidelines and laboratories SOPs. . Sound knowledge of HPLC, GC, IR, MS, UV/VIS spectrophotometer, Karl Fischer, AES, AAS, ion chromatography, viscometer and TLC. . Preparation of mobile phase, dissolution media. ... - 2012 Dec 19

Quality Control Management

Lewis Center, OH, 43035
... An individual having a good skill of writing SOPs Protocols and User Requirements Specification as per FDA guidelines, GMP and GLP,21CFR. SKILLS • Expertise in testing of raw materials and finished products by HPLC, FT-IR and Titration Assays with ... - 2012 Jun 26

Engineer Customer

Reynoldsburg, OH, 43068
... Performed validation work in accordance to Good Laboratory Practices (GLP) and laboratory Standard Operating Procedures (SOP). . Created documentation for some Standard Operating Procedures involving the use of the HPLC system. EDUCATIONAL AND ... - 2011 Feb 05

Customer Service Assistant

Columbus, OH, 43201
... Trained in GLP and cGMP practices . Proficiently head multiple bioassay studies according to registered SOPs . Direct trainer and responsible party for teaching and qualifying technical skills . Consult with supervisors, managers and peers affecting ... - 2010 Sep 30

Project Manager Quality Control

Columbus, OH, 43206
... ********, **** 43206 419-***-**** + abknnv@r.postjobfree.com Professional Profile Self-motivated professional with extensive knowledge of FDA 21 CFR, GMP, GLP, GCP and ICH Quality and Regulatory compliance. An organized and versatile individual who ... - 2010 Sep 28

Technician Management

Columbus, OH, 43235
... Extensive experience with GLP/GMP/ISO standards, EPA, FDA and USDA regulations. . Trained in the manifestation and prevention of multiple biological pathogens and chemical agents, including: Herpes B Virus, Tuberculosis (TB), HPAI, Yersinia Pestis, ... - 2010 Mar 09

Clinical Quality Assurance Auditor - Compliance

Columbus, OH
... Summary • Strong knowledge of FDA, ICH-GCP, GMP, GLP, 21 CFR Part System, ISO 9001:2000 & European regulations (EMEA) • Experience with regulatory documentation and IRB submissions for site compliance per protocols • In depth understanding of ... - 2009 Sep 20
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