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Understand and run HPLC, GC, ICP, UV, FTIR, Dissolution tester, and other analytical instrumentation in an analytical lab setup. Experience with analytical instrumentation, such as HPLC, GC, CE, ICP, FTIR, and dissolution apparatus in a GMP environment.
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The Analytical Research and Development Chemist will work with an assigned project team of chemists in the laboratory to analyze and develop HPLC and GC methods for assay, impurity and dissolution testing of pharmaceutical finished dosage forms.
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The client is seeking a Research Associate with a background in analytical chemistry for a contract position. Assist in the development of new HPLC/GC based analytical methods. Hands-on experience characterizing small molecules by HPLC (High performance liquid chromatography) or GC (Gas chromatography) and generating reports for broader team consumption.
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Solid knowledge of analytical chemistry, materials science & physics required. Our site in Burnet, TX is seeking an Analytical Operations Lab Manager to join our team. Knowledge of proper controls for analytical instrumentation, SPC, stability, accuracy, variation, and method uncertainty and GR&R required.
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Technical Proficiency in analytical method development, including dissolution testing, chromatographic techniques (such as HPLC, and GC), and spectroscopy method (such as UV-Vis, NMF, MS, a long with expertise in method robustness and qualification/validation requirements.
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Support IFRS/STAT Reporting, Financial Plan/Capital Reforecast with hedge-related inputs.
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As an Analytical Development Senior Scientist, you will be responsible for method development and validation to support process development, tech transfer, release testing and stability activities for pharmaceutical drug product programs.
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This position is responsible for directing all aspects of CMC (Chemistry, Manufacturing and Controls) for pharmaceutical drugs and agents as well as the analytical work associated with that CMC across all of the small molecule projects within Pharma Cinq and, potentially, gene therapy projects.
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Under the general supervision of the Director, Analytical and Regulatory Affairs of Regulatory Affair and Quality Control, the Analytical Development Chemist is responsible for developing and validating analytical methods, writing and establishing specifications, and performing trial pharmaceutical product testing.
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Operate analytical instrumentation such as HPLC, GC, GC/MS, FTIR, Titrator, Particle Size Analyzer. Actively participate in teams assembled to investigate and solve analytical technical issues within Analytical Development, Chemical Development, Process Support Group and Quality Control.
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Under the direction of and reporting to the Supervisor of Maintenance, the Senior Analytical Electrician is responsible for all aspects of installation and repairing of electrical equipment. This includes but is not limited to motors, breakers, drivers, PLC controls, various sensors/switches, and associated programming needs.
$38 an hourFull-timeExpandApply NowActive JobUpdated 19 days ago - UpvoteDownvoteShare Job
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In-depth knowledge of common analytical techniques used in the bio-pharmaceutical industry such as iCIEF, UPLC, CE, Bioassay, ELISA, LC-MS etc., method qualification, method development, and method transfer.
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Gowan Company is looking for an Analytical Chemist to work within our Research and Development group. An Analytical Chemist will collaborate with group members to continue the tradition of scientific excellence in which timely, high-quality results allow the Gowan Company to make sound business decisions with the highest confidence.
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Kelly Science & Clinical has a new, temporary opportunity for an Analytical Chemist in Gurnee, IL! Conduct installation, operational, and performance qualifications for analytical equipment, specifically FTIR (Fourier Transform Infrared) and GC-FID (Gas Chromatography with Flame Ionization Detector.
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The Quality Control Analytical (QCA) Analyst is responsible for performing analytical test methods on in-process intermediates and varying stages of drug products under minimal supervision and within cGMP guidelines, to support further manufacturing of commercial and clinical therapeutics.
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Title: analytical Company: Zeichner Risk Analytics Zra
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