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Online Resumes with "GLP regulations"
GLP Quality Assurance Auditor
Promote compliance with all GLP regulations, including IACUC and internal policies, procedures, state and federal regulations. Audited complex systems, facilities, study protocols, validation plans, raw data, in-life critical phases and final reports in the ABSL-2, 3 and 4.
Scientist
Some highlights of my career include: Substantive research experience involving macromolecule synthesis, molecular assays, immunodetection, nanotechnology-based biosensors, surface chemistry, self-assembled monolayers (SAMs), surface coating including plasma deposition and micro-fabrication. Proficient in synthetic chemistry with 4 years of experience in organic synthesis plus a Master degree in Organic Chemistry. Exp...
Senior IT Manager and Pharmaceutical Scientist--15 years Experience
A highly experienced and hands-on technical IT project manager and laboratory automation scientist with in-depth knowledge of the SDLC and pharmaceutical regulations (ie. 21 CFR part 11, and GLP regulations). 15 years of experience.
Tags for this Online Resume: New Jersey, Pharmaceutical, Automation, Technical Lead, Laboratory
Research
To obtain a challenging position within the Pharmaceutical industry or medical devices industry that will allow me to use my experience to play a key role in Clinical Research studies and projects, and/or product development with medical devices.
Tags for this Online Resume: Clinical Pathology, laboratory method development, IQ, OQ, PQ, instrumentation, validation of medical devices, Regulatory, GLP, GCP, IRB, TMF, Project Manager, Documentation Specialist, Scientist, Archives
Clinical Research - 20 Years of Experience - Near 01950
Tags for this Online Resume: Full knowledge of drug devolopment, Certified GCO, GMP, GLP regulations and very educated in tegulations, Have worked in everyday practice , Sierector, QA Drug Supply Management and manufacturing regulations, hard worker , extremely dedicated
Biochemist - 13 Years of Experience - Near 17036
Professional Summary: Accomplished in biochemistry, chemistry, protein biochemistry, structural biology, biophysics, molecular biology, enzymology, carbohydrate chemistry and glycobiology. * Great team player with a proven record of first author publications. * Highly motivated scientist with innovative problem solving and critical thinking capabilities. * Proficient in High-throughput screening assays for drug discovery & ...
Tags for this Online Resume: High Performance Liquid Chromatography (HPLC), Research, Derivatives, Chemistry, COLI, Documentation, Electrophoresis, ELISA, Good Laboratory Practices, Good Manufacturing Practices
Chemist - 20 Years of Experience - Near 95127
SUMMARY Performed work in compliance with EPA, ISO, cGMP and GLP regulations and SOP's. Conducted chemical analysis using various analytical instrumentation and measurements. Supported production and research providing fast, friendly service. Maintained inventory of chemicals for department and ensured that it was clean and safe work area. Monitored hazardous waste container and had container remove as necessary. Experience...
Tags for this Online Resume: Benefits, Accounting, Administrative Assistant, Attention to Detail, Certificate Authority, Chemistry, Compliance, Good Laboratory Practices, Hazardous Waste, High Performance Liquid Chromatography (HPLC)
Quality Engineer - 10 Years of Experience - Near 63136
CAREER SUMMARY: Quality Specialist Professional with strong analytical skills in various lab settings such as environmental, animal, clinical and pharmaceutical. Experienced in research, laboratory, QA/QC, auditing, Quality measurement systems and technical writing. Familiar with GMP/GLP regulations in cGMP/cGLP manufacturing environment, EPA, FDA and CFR guidelines. Comfortable working in fast paced, priority shifting and ...
Tags for this Online Resume: Compliance, ISO, ISO 9000, Occupational Safety and Health Act, OSHA, Protocol, Research, Good Manufacturing Practices, Management, Research and Development
Chemist - 20 Years of Experience - Near 53701
I am a Chemist with 20 years of pharmaceutical CRO experience. I have developed and validated ~ 75 methods for the analysis small molecule pharmaceutical compounds in biological fluids using LC/MS/MS. I have experience in most aspects if the industry, including project management, and study director roles.
Tags for this Online Resume: LC/MS/MS, Analytical Method Development, GLP regulations, Validation , Project management, SPE, Data Processing, Documentation, Project Manager, Analytical Chemistry
Chemist
Summary * Experienced Quality Assurance scientist in the pharmaceutical and biotechnology industry working for over 17 years in a cGMP and GLP regulated environment. * Lead efforts in the business analysis for the group's business continuity program and the implementation of the Laboratory Information Management Systems (LIMS). * Knowledgeable in Project Management methodologies like 5S, LEAN and Six Sigma. * Skilled in ana...
Tags for this Online Resume: High Performance Liquid Chromatography (HPLC), Microsoft, Microsoft DOS, Microsoft Windows, Applications, Benefits, Business Analysis, Business Analyst, Documentation, Information Technology, pharmaceutical, sap
Biochemist - 15 Years of Experience - Near 92129
SUMMARY Research and development scientist with a broad technical expertise in microbiology and molecular biology in the Biotechnology and Pharmaceutical industry Multiple years of bench/hands-on extensive experience in microbiology and molecular biology for in vitro diagnostics assays (IVD) development for infectious diseases, food borne pathogen detection, genetic markers in field of oncology. Performed classic and molecu...
Tags for this Online Resume: Research, Atlas, Automation, Integrate, Microbiological Testing, Protocol, Test, Cancer, Diagnostics, Documentation
