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Online Resumes with "GMP GLP"

Analytical chemist

Leading analytical chemist

Tags for this Online Resume: Analytical chemist, method development, validation, transfer, multiple instruments, GMP/GLP release and stability testing, CMC development process, Specification, SOP, Stability, LIMS, contract laboratories/manufacturing, Regulatory filing documents

Regulatory Pharmaceutical Document Specialist and Technical Writer

Brenda is a Technical Writer and Quality Assurance Regulatory Document Specialist with over ten years of experience in the pharmaceutical industry. She has extensive experience with all types of document project work, including writing, editing, formatting. She has experience as a team member for non-conformance investigations (NCs) and Corrective Action and Preventative Actions (CAPAs). Her analytical and research skil...

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Sr Staff Scientist, Associate Director, Director, Bayarea, CA

Tags for this Online Resume: mass spectrometry, GMP/GLP, protein characterization, IND filing, Glycosylation, high through-put assay

Chemist/Associate Scientist

Method Development, Validation, GMP and GLP Compliance

Ideal Companies: Genentech, Amgen, Guidance, Gilead Science, Abbott

I have extensive Chemical and Biological experience with a working knowledge of USP and cGMP and GLP. I have 12 years of Laboratory experience in Chemistry, Biology, Microbiology and Textile industry. I have repaired and operated Caliper (Sotax) Tablet P

To advance career as a scientist where my education, experience and motivation will have a valuable application for company and personal growth.

Tags for this Online Resume: HLPC, Dissolution/EMC, Wet Chemistry, Vitek , Autoclave/Kaye Validation, Qualified Trainer/Reviewer/Documenation

Associate Scientist, Union City

I have two years of laboratory experience utilizing sterile technique, and ten months of experience in a cGMP/GLP laboratory environment preparing human serum and urine samples and operating chemistry analyzers. I am passionate about teaching and learning, and am currently continuing my education with a certification in Biotechnology at Ohlone College. I am also interested in obtaining a Clinical Genetic and Molecular Biolo...


I have 14 years of experience in pharmaceutical industries. Results oriented individual with a track record of instituting and maintaining high levels of Quality Assurance and leadership. I’m seeking additional opportunities for professional development in consulting, validation, compliance or technical areas. Strong analytical and planning skills. Six Sigma Black Belt trained. Knowledge in FDA, cGMP, GLP, 21 CFR - Part 820...

Ideal Companies: Pharmaceuticals or food industries

Tags for this Online Resume: qa, validation, lims, qc

Quality Assurance Associate Managert

Quality Assurance professional with problem-solving abilities in Pharmaceutical and Biotechnology industries. Primary strengths include US (FDA) 21 CFR, and ICH Q7A Guidance for API Manufacture, Quality Systems development and implementation and strong auditing skills. Introduced and managed electronic document management software including validation, implementation, and maintenance, as well as project team leadership. R...

Tags for this Online Resume: Quality Assurance, FDA regulations, CAPA, Document Control, Change control

Director of Quality Systems & Scientific Affairs, 20 years experience in food, dietary supplements and cosmetics

Tags for this Online Resume: CQM-OE ASQ Certified, FDA Regulated Industries, GMP, GLP, SOPs, HACCP Experience , Influencial Leader, Driven by goals, Motivated by results

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 Cell Culture Scientist- CSO

Julie Bick has been associated with the pharmaceutical industry for 12 of her 17 year career in the life science field, working with two of the leading global drug development companies. Julie has developed a wide range of skills while researching diverse areas of biochemistry and cell biology, from antibody and protein engineering to cell culture optimization and assay development. These efforts have been supported by her ...