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Online Resumes with "GLP"
GCP Auditor - 9 years experience, Monterrey, Mexico
Tags for this Online Resume: GCP Auditor, Clinical Auditor, GLP Auditor, Quality Assurance, Clinical Trails, Good clinical practice
Analytical Research and Development and Quality Control Director, open for relocation
Tags for this Online Resume: Analytical R&D, Analytical Quality Control, Cost conscious, Timely delivery, Team building, GLP, cGMP compliance
Medical Device Project Manager, Indiana
Seeking a position with a start up or established company where I can apply my diverse management and quality compliance experiences and skills to further my professional and personal growth.
Tags for this Online Resume: Medical Devices , Project Management, Veterinary Technology , Communication , Biomedical Leadership & Training , Preclinical & Clinical Trials , Safety Protocols , Regulatory Compliance Process Improvement , Facility Management , Research, Quality Assurance , Regenerative Medicine, Product Development , Supply Chain Management , Vendor Relations, Strategic & Tactical Planning , ISO 13485, GMP/GLP/GCP, Administrative
Senior Analytical Chemist - Management Experience
Tags for this Online Resume: Chromatography, HPLC, Spectroscopy, Organic Synthesis, Wet Chemistry, ISO 9001, GLP, GMP
GLP Quality Assurance Auditor
To work in a challenging atmosphere that provides me ample opportunity for learning and growth and to carve a niche in whatever I undertake.
Tags for this Online Resume: Quality Assurance, GLP, non clinical, preclinical, toxicology, Auditor
VP Quality and Compliance - GCP, GLP, GMP, PV; Pharma and Med Device Experince
Highly experienced biologist with in-vivo/ in-vitro and analytical study conduct/ monitoring
I am seeking a position where I may utilize my skills and gain new responsibilities.
Tags for this Online Resume: Quality, study director, analytical , metabolism, development, GLP/ GMP experience
Quality Control Professional, Medical Scientist 11 years experience
I'm a Bilingual Medical Scientist with pharmaceutical experience in quality control, GLP, GDP, GMP immunoassay testing, laboratory investigations, and exception reporting. 10 years experience in Clinical and Research applications of microbiology, phlebotomy, safety, risk assessment and mitigation, process improvement and employee development.
Tags for this Online Resume: Quality Control Associate, Medical Scientist, Medical Technologist, Research Associate, Environmental Monitoring, Microbiology
QC/Research/ Analytical Chemist
Expert in testing Biologics & Pharmaceuticals within Quality Control Chemistry & R&D chemistry Labs. Professional using HPLC, UV, FTIR, SDS-PAGE, GC, TOC and much more. Also has broad experience with GDP, GLP & cGMP. Used iLIMS, LIMS, ISOTrain, Shimadzu Class-VP sofware, HP Agilent, Millinium softwares, Empower.
Tags for this Online Resume: QC Analytical Chemist, QC Research Associate , R&D Chemistry Lab
Director of Land Development and Construction
I would like to be in charge of all field construction from concept to completion; running multiple sites.
Ideal Companies: I would like to work for a nice mid size developmnet company that has its own in house construction department
Tags for this Online Resume: Senior Project Manager, Director of Land Development and Construction VP
Pre clinical Researcher, Phd Pharmacology & Toxicology
To undertake a challenging career in the field of research related to Pharmacology and Toxicology including pre-clinical research, drug metabolism and pharmacokinetics, clinical writing and documentation of scientific data by using cutting edge technologies for finding successful solutions to problems.
Tags for this Online Resume: toxicology, preclinical research, diabetes research, drug safety, toxicity testing, GLP
Clinical Research Professional- 20 years experience- Memphis
Clinical research professional with over 20 years of experience in both industry and academia. Responsible for all audit activities for multiple phase 1-3 clinical trials. Responsibilities include but are not limited to ICH/GCP compliance. Reviews key study documents such as protocols, informed consents, CRFs, monitor reports, and CSR. Presents protocol and GCP training at Investigator meetings. Mentors and trains junior qu...
Tags for this Online Resume: GCP, FDA submission documents, Drug safety, GLP, NDA, Auditor
