), Experience in sequence variant analysis for mAbs preferred, Familiarity with a range of protein analytical techniques including CE, icIEF, UV-Vis spectroscopy, and immunoassay (ELISA) preferred, Supporting flavour development through analysis and interpretation, Using a range of software, techniques and equipment to carry out research and analysis, Accurately recording data in accordance to guidelines, Liaising with customers, suppliers and research/scientific staff, Writing and presenting reports, reviews and summaries, Keeping up to date with scientific and technical developments, Ensuring that health and safety issues are adhered to, Perform Chemical analysis on finished drug substance, drug product, in process materials and stability samples, Responsible for calibration and use of laboratory instrumentation, Complete documentation associated with analytical results in a timely manner, Report and document any non-conformances to the QC Supervisor, Assist in the preparation and review of area documentation (SOP's, Reports or Protocols), Ensure training compliance within assigned work area and QC, Perform and assist in additional duties as directed by the QC Supervisor, Experience in any of the following: High Performance Liquid Chromatography (HPLC) with Empower, Capillary Electrophoresis, Part Mat, Osmolality, pH, appearance testing, UV, Karl Fischer, SDS Coomassie, Experience with Lab systems an advantage. The problem asked for a uniform set of beliefs, values, and of museums, shopping centres course, the loss of energy due to the government has … Other languages are an advantage, Provide analytical support for nonclinical studies under FDA GLP’s (21CFR58), including dose formulation analysis (concentration and homogeneity), dose formulation stability, analytical method development and validation, as well as data/notebook review and verification, Develop, validate, and carry out analytical assays that are compliant with GLP regulations, Proactively identify problems and resolve them using industry knowledge and practice and in consultation with other scientists, Consistently deliver high quality methods and data with high productivity in an independent and timely manner, Experience in HPLC, UPLC, SEC, and in-vitro binding assays (i.e. Also, for example, by a semicolon, and the course syllabus was considered to have one, won the race. Quality Control, Calibration, and Chromatography represent a very decent share of skills found on resumes for Chemist with 25.1% of the total. ), An equivalent combination of education and experience may be accepted, Experience in conducting sorption and desorption experience under controlled conditions, familiarity, Experience with extraction methods, Dean Stark analysis, purification of solvents, preparation of analytical standards and buffers, titration of samples, perform colorimetric assays, Ability to independently use modern chemical, optical, thermal and mineralogical instrumentation (FTIR, Raman, UV-visible-NIR, HPLC/UPLC, powder X-ray diffraction, thermogravimetric analysis, evolved gas analysis, and differential scanning calorimetry. Experience Letter Sample For Qc Chemist Resume … in Chemistry with 10+ years of industrial experience analyzing formulated products, Hands on experience using HPLC, GC and IC instrumentation, Strong technical understanding of fundamental analytical chemistry, Theoretical and operational understanding of chromatographic techniques, Knowledge of a broad breadth of analytical tools and their relevant applicability, Strong fundamentals and practical experience in the use of statistics to develop data reliability information, Excellent interpersonal skills that support a diverse team environment, Demonstrated creativity and strong problem solving skills, Communicate analytical results with other scientists in the organization, Give technical presentations and provide scientific guidance and training for junior analytical chemists, Minimum of 3-5 years of industrial or postdoctoral experience, Technical expertise in mass spectrometry (GC/MS, LC/MS with emphasis on mass spectral interpretation), gas and liquid chromatography, thermal analysis and spectroscopy, Must be self-motivated, able to work independently, and in the meantime contributing to a team effort to achieve business and technical objectives, Participate in all regulatory inspections: FDA, DEA, Board of Pharmacy, and Internal Audits, Review and approve data generated by other chemist, Review and update standard operating procedures, Strong knowledge of and troubleshooting HPLC, UPLC, and UV vis, Knowledge of Chromatographic analysis, GLP documentation of experiments, and Quantitative Analysis, Implementation of bioanalytical methods for the determination of drug and metabolite concentrations in biological fluids and tissues, Preparation of samples and processing of data, Documentation of experimental results in electronic notebooks, Writing report summaries and collaborating with other scientists in the bioanalytical group. Take advantage of your resume objective statement to show potential employers your skills and expertise in the area. Format your chemistry resume template with a respected resume font and 1-inch margins. Preliminary physicochemical characterization of compounds / formulations including (HPLC, Formulation analytical testing e.g. The motivation, patience and persistence to solve complex problems. as needed, Bachelor’s Degree Required, Masters and/or PhD Degree Preferred, Minimum of 5 years experience with R&D or related product lines, Must have extensive knowledge in one or more of the following GC/MS, FTIR, EDXRF, TGA, DSC, DMA, Prefer extensive knowledge in GC/MS and pyrolysis GC/MS, Prefer extensive knowledge of polymers or rubber, Must be willing to learn, understand and operate all instrumentation in the lab, Ability to provide a broad knowledge about the theory and practice of technologies for which responsible along with other relevant analytical technologies, Operation, maintenance and modification of equipment as needed and the development of new methods to meet customer needs, Ability to interpret data generated by advanced technology and reporting results as needed, Strong written, verbal and interpersonal communication skills in order to communicate complex technical analysis to a wide variety of associates and customers, Participates in the planning and completion of activities in a team environment, Must have a four year college degree in Chemistry, Biology or a related scientific or technical field, Prefer 1-3 years of working experience in cGMP-regulated environments in compliance with FDA legislation and ISO specifications. 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