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Online Resumes with "Glp"



Scientist, Molecular Biology, Virology, GLP/GMP, Validation, Diagnostics, Assay/Process development

Scientist with broad-based experience in Diagnostics and Pharmaceutical R&D. Proven skills in Assay/Process Validation, PCR/RT-PCR/qPCR, Luminex Multiplex Technology and Virus Inactivation/Removal study. Experience in: Assay and Process Development/Optimization, Production Scale down, Microbiology/Virology, Molecular/Cellular Biology, cGMP/GLP/GDP, Troubleshooting

Tags for this Online Resume: Molecular Biology, Virology, PCR/RT-PCR/qPCR, Assay development/validation, Process development/validation, QA/QC, Virus removal/inactivation

People, projects and laboratory equipment management

Highly accomplished PRODUCTION and PROJECT MANAGER with multi-Project Management experience in the Pharmaceutical/Biotech Industry (Generic Drug Production, Drug Discovery, Assay Development and High-Throughput Laboratory Automation and equipment). Proven track record in the arena of Robotic Engineering including on-time delivery of custom Automated Robotic Screening Platforms for High-Throughput Screening (HTS), as well as...

Ideal Companies: People, projects and laboratory equipment management (including but not limited too market analysis, ordering, installation, operation, maintenance and removal from operation).

Tags for this Online Resume: project management, HTS, screening, robotic , laboratory equipment, biology, chemistry , pharma, Environmental Health and Safety, pharmaceutical , academic, Drug Discovery, automation

SCIENTIST

To excel as a Analytical chemistry scientist.

Tags for this Online Resume: HPLC, GC, FTIR, UV-VIS, KF AUTOTITRATORS, GLP

Featured Profile

Versatile Bio-Tech Researcher w/ real leadership experience!

Supervise a team of technicians with various certification levels. Responsible for overall management and conduct of all studies assigned to Large Animal Group. Assumes fiscal responsibilities for assigned studies, is aware of study timing and materials need projections. Acts independently carrying out all in-life study functions as assigned. Ensures that duties are performed according to protocol requirements and adher...

Ideal Companies: Novartis, Pfizer, Abbott, Johnson & Johnson

Tags for this Online Resume: Detailed-Oriented, Leader, Problem Solver, Passionate, Clear Communicator

Regulatory Affairs Associate, New Jersey

Regulatory Affairs professional with a strong regulatory and compliance foundation, well-versed in the laws, regulations and requirements of the FDA; over six years of experience as an International Coordinator for a pharmaceutical organization, currently completing a graduate degree in Regulatory Affairs in Drug Development, Biologics and Medical Devices, studying all facets of regulatory requirements including processes a...

Principal Scienitst - Medical Device, Pharmaceutical

Principal Scientist position in phamaceutical/biotech or medical device company. Will reply to Manager or Asscociate Director positions.

Tags for this Online Resume: Preclinical, Study Director, Innovative, Liaison, GLP, Leadership

Clinical Research Scientist, New Jersey

Extensive experience in both the pharmaceutical industry and academia, with a proven record of success in developing and validating assays from drug discovery through early clinical stages. Recognized as a group leader and team player, considered reliable, self-motivated, and adaptable embracing challenges with outside of the box thinking. Particularly effective at multitasking, overcoming obstacles and handling the pres...

Tags for this Online Resume: ELISA, MSD, PK, Biomarkers, GLP, Flow Cytometry, CRO, Outsourcing, Flow Cytometry, Assay Development, Validation

Senior Scientist - 13 years experience in academia and industry - GLP experiecne, - preclinical characterization of nanomaterials and biotechnology-derived pharmaceuticals - bioanalytical assay development and validation - project design and staff managem

seeking vertical move in my career; looking for a job where I can use my current scientific and managerial knowledge and experience and to further develop it; I am looking for associate director, director, principal scientist or scientific officer position in the area of immunology, immunotoxicology, nanoimmunotoxicology or nanotechnology/nanomedicine. I am working curently in Frederick MD, but I am open for a good employme...

Tags for this Online Resume: nanoparticles, immunology, toxicology, nanotechnology

Research Assistant II, Regulatory Contact-QA collaborator

With a total of 4 years of laboratory work, I improve my skills as a Research Collaborator. I extend my competences on regulatory field, working on IRB approval and regulatory studies. I am GLP certified so I want to extend my carrier on a higher level. I wish to do more Regulatory and QA duties. I am more than motivated to take a position as a Manager.

Tags for this Online Resume: Bioch, Biochemistry, biotechnology, Research Assistant-highe expertise, regulatory, immunology, Quality Assurance

QA/QC SUPERVISOR

To ensure a challenging position commensurate to my qualification where I can effectively contribute my knowledge in Quality Control, Quality Assurance, ISO, HACCP,GMP, GLP, supervision and other experiences.

Tags for this Online Resume: GRACE, CELIZ, BEDIA, MICROBIOLOGIST, QA/QC SUPERVISOR, ANALYST, GRACE CELIZ BEDIA, LABORATORY ANALYST, QC SUPERVISOR, TEACHER

Consultant, pharmaceutical industry

I have been an effective manager/director of numerous functional areas, and have consulted internationally in cGMP/GLP/QA issues. I seek to continue using that skill set.

Tags for this Online Resume: compendial affairs, expert witness, pharmaceutical consultant, network science, compendial microbiology, general physiology

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