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Online Resumes with "HPLC METHOD DEVELOPMENT"
Senior Research Chemist
HPLC methods development and validations. Dissolutions
Research scientist-3 years experience-HPLC-MS method development and validation
Aspiring for a growth oriented career in an organization that is progressive and offers a challenging environment wherein I can utilize my skills and experience for the growth of the organization, develop quality pharmaceutical products, and contribute the best of my services for mutual benefit.
Tags for this Online Resume: analytical chemist, medicinal chemist, HPLC METHOD DEVELOPMENT, Method validation, analytical research chemist, GC-FID; GC/MS, FTIR, LCMS
Analytical Chemist, Baltimore
HPLC analysis, Method development, Method validation, QC Chemist, analytical chemist, HPLC method development and validation
Biochemist II
I would like to work for a large bio-pharmaceutical company in the Maryland/DC area. I am currently a Biochemist II and would like to become a research associate.
Ideal Companies: MedImmune, Novavax, NIH, Otsuka
Tags for this Online Resume: HPLC, GMP, ELISA, Method Development, Validation, Characterization, GLP, Microsoft Office, DNA Purification, Dissolution, Capillary Electrophoresis, Cell Culture
Bioanalytical Research Associate- mass Spectrometry
Seeking to contribute to a Bioanalytical R & D in a Pharmaceutical/ Biotech company/ lab where I can utilize my strong background in analytical instrumentation and can engage in LC-MS/MS and HPLC method developments and validation and Bioavailability/ Bioequivalence studies.
Tags for this Online Resume: Mass Spectrometry, LCMS, Bioanalytical, Method development, LC-MS/MS, chromatography
Quality Specialist
Analytical chemist position with a solid, well-established company within an environment conducive to continued personal and professional growth in the field focusing on: method development; method transfers; validation; writing of protocols and SOPs; instrumentation(HPLC, IC, GC, AA, IR, NMR, MS, GC-MS, LC-MS).
Ideal Companies: Biogen Idec, KBI, Novo Nordisk
Tags for this Online Resume: Method Development, Method Transfers, GMP/GLP, Validation, HPLC, GC, IC, AA, GC-MS, LC-MS, TOC, Conductivity, Project Management
Scientist, Director, Entrepreneurial, PhD, MBA, R&D strategy, Startups, Strategic & Technical Planning, Healthcare, Biomedical, Business Development, Commercialization, Product Development, Grant & Funding, Operations, Management, Manager
To undertake a suitable position in a healthcare, biomedical, Clinical Research, bio-pharmaceutical or biotechnology organization that capitalizes on my extensive scientific, drug development, business and early stage start-up managerial experience. I have many years of practical, hands on experience on both sides of the value equation in life science - as both an academic researcher and also as a NC Biotechnology Center-in...
Ideal Companies: Medical Centers, Academic Medical Centers, Small-Mid Size Companies (Biotech, Pharma, Diagnostics and Medical Devices), Consulting firms, Clinical Research, Clinical Trials, Clinical Data Management, Research based institutions...
Tags for this Online Resume: proteomics, biological research, molecular biology, drug metaboilsm, cell culture, assay development, Early Stage, Startup, Start-up, Business Development, Pharma, neuroscience, management, healthcare, healthcare management, clinical trial, clinical research, Translational, animal model, Research and Development strategy
Laboratory Manager - 18 Years of Experience - Near 28037
Qualifications Summary Laboratory Manager with extensive experience in regulated pharmaceutical manufacturing and research and development with more than 10 years of management experience. Thorough understanding of regulated Laboratory environments including but not limited to GMP, GLP, GDP and 21 CFR Part 11. Quick learner with proven track record of driving success. Skilled at navigating FDA and vendor audits. Implemented...
Tags for this Online Resume: Project Leader, Project Management, Budgetary, Drafting, High Performance Liquid Chromatography (HPLC), Management, Planning, Rational, White Papers, clinical, phase, trial, gcp, protocol, pharmaceutical, Quality, LC/MS
System Administrator - 0 Years of Experience
Life cycle Management and documentation of specification in Laboratory Information Management Systems (LabWare LIMS) in cGMP environment. * Create and Manage Drug substance, Drug product, and Raw materials specifications in LIMS against the master specification copy available in the Document management system. * Accurately configure Analysis's including Strength, Impurities content, Water content, Content uniformity, Resid...
Tags for this Online Resume: Acceptance Testing, Audit, Configure, Document Management, Documentation, Good Manufacturing Practices, High Performance Liquid Chromatography (HPLC), Management, Manufacturing, Pharmaceutical Industry
