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Online Resumes with "GLP "



Industrial Microbiologist

To obtain a Food Safety Scientist position that will utilize my extensive Biomedical/ Pharmaceutical, Food and Manufacturing background and education. Experienced with FDA, EU, GLP, GMP, ISO 9001, HACCP and CFR requirements.

Scientist - 8 Years of Experience - Near 95695

PROFILE: 8+ years of success in biologic research, data analysis, project management and leadership, scientific writing and editing, teaching and mentorship, and collaborative biomedical-based engineering in university and lab settings. * 6 research publications, highlighting advancements in bone tissue engineering and biopharmaceutical delivery. * Podium presentations at seminars and conferences focusing on scientific netw...

Tags for this Online Resume: Manufacturing, OSHA, Research, Cellular, Good Manufacturing Practices, Project Management, Project Manager, Biomedical Engineering, Materials Science, Biomaterials, Science, Biomedical, Pharmaceutical, Cell culture, Scaramento, Tissue engineering, Tissue culture, Laboratory

R&D Scientist/Chemist

CAREER HIGHLIGHTS Systematic approach & dedication resulted in completion of key project milestones before deadline. Instrumental in formulation and development of consumer products as well as improving the current products for a world leading FMCG company. Championed the art of enzyme stability testing initially under supervision and then on own initiative. Got recognized for the post-graduate project due to significant im...

Tags for this Online Resume: Product Design, Audit, Chemistry, Product Development, Test, Test Plans, Applications, Centrifuge, Consumer Products, Good Laboratory Practices

Veterinary Technician

Summary of Qualifications Accomplished laboratory animal veterinarian with 15+ years of experience working in academia and in the biotech industry. Proven ability to communicate with staff at all levels of an organization, and with scientific and non-scientific backgrounds. Experienced at working under USDA, APHIS, DEA and GLP requirements, with expertise in the management of support staff and animal colonies in AAALAC accr...

Tags for this Online Resume: Imaging, Radiation, Surgery, Surgical, Toxicology, Biomedical Industry, Training, Academia, Laboratory Animal Medicine, Veterinary Medicine, Nonhuman Primates

Chemist

QUALIFICATIONS * Currently working toward the Regulatory Affair Certificate. * Extensive analytical characterization and data interpretation skills. * Experienced in very different analytical tests like Assay, Release Rate, Residual Solvents, Water Content Determination, and ID by IR, and Viscosity Testing. * Expert in handling different analytical apparatus like HPLC, GC, FTIR, UV-VIS, Karl Fisher, Colorimeter, pH meter, L...

Tags for this Online Resume: Good Manufacturing Practices, Manufacturing, Compliance, Inventory, Microbiology, Research, Quality Assurance, Test, Chemistry, High Performance Liquid Chromatography (HPLC)

Study Coordinator

Summary Study Coordinator with 6 years' experience specializing in technical support of animal studies requiring GLP compliant interpretations, analysis, documentation, and reporting of results per FDA regulations beginning with protocol development support and creation of shell reports resulting in a Final product ready for FDA Regulatory Filings. Areas of Expertise / Core Competencies * Highly dependable, focused and dete...

Tags for this Online Resume: Documentation, Good Laboratory Practices, Protocol, Analytical Skills, Biomedical Industry, Quality, Quality Assurance, Coordinator, Medical Devices, Regulatory

Quality Engineer - 19 Years of Experience - Near 77459

SUMMARY Highly motivated, goal oriented, and efficient Quality Assurance professional with expertise in regulatory compliance, documentation, auditing, and process improvements. Known for ability to complete multi-faced tasks within strict time constraints. Demonstrated expertise in setting priorities and establishing appropriate detailed documentation to meet deadlines using strong clinical, analytical, and technical skill...

Tags for this Online Resume: Quality, Quality Assurance, Quality Control, Audit, Complaints, ISO, ISO 9001, Management, Protocol, Manufacturing, ISO 13485

Biological Technician - 20+ Years of Experience - Near 94952

PROFESSIONAL SUMMARY Thirty years experience in Immunoassay, DNA hybridization, and qPCR assay development DNA and protein isolation, purification, labeling and characterization hybridoma/monoclonal antibody technology in the diagnostics and therapeutics industries. GLP documentation Proven record in meeting timelines and bringing products to market. Excellent written and verbal communications skills.

Tags for this Online Resume: Diagnostics, Assay Development, Validation, SOP, Antibodies, Hybridoma, Protein Purification, Bioanalytical Research, DNA, PCR, Watson LIMS, Sample Analysis, Cell Culture, Immunogenicity, Serum Drug Concetration, Protein Characterization, DNA Characterization, San Francisco

Clinical In-house Monitoring - 6 Years of Experience - Near 07621

SUMMARY OF QUALIFICATIONS Pharmaceutical professional with 5+ years of clinical research experience in management and monitoring. Seeking new and exciting opportunities in new therapeutic areas to expand my expertise. Known for building strong relationships with clients and partnering with management teams to ensure quality services, compliance and efficiency. Manage Clinical Research, third party vendors, and clinical inst...

Tags for this Online Resume: Fraud, ICD-9, Insurance, Medical, Query, Management, Good Clinical Practices, ICH, Documentation, Clinical Research

Clinical Regulatory Affairs - Boston Area

Tags for this Online Resume: IRB, FDA, Clinical Research, Unix, Regulatory Affairs, NDA, GLP

Electromechanical Equipment Assembler - 1 Years of Experience

SUMMARY: * More than 5 years of Experience in cGMP regulated environment. * Manage control of changes, Deviations, OOSIR and CAPA * Review batch records and releases lots * Prepare and revise Standard Operating Procedure for cGMP Equipment * Work both independently and in team to finish project on-time. * Knowledge of FDA regulations and 21 CFR 210 & 211, cGMP/GLP/GDP guidelines for solid and liquid drug products.

Tags for this Online Resume: Manufacturing, Packaging, Documentation, Management, Quality, Quality Assurance, Quality Management, Test, Audit, Quality Control