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Preferred to have working experience in a GLP labs and familiarity with use of LIMS. You will be a member of Specialty Bioanalytics, which plays a critical role in development of biological therapeutics from late stage of research, IND enabling GLP studies, clinical trials through BLA submission and post marketing support.
Full-timeExpandApply NowActive JobUpdated 29 days ago - UpvoteDownvoteShare Job
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Ensure that GLP regulations and SOPs are followed in all bioanalytical service activities. Associate Scientist / Bioanalytical Services Essential Functions Provide support for running sensitive, reliable and efficient LC-MS/MS bioanalytical assays for TK/PK assessment.
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We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development.
$23 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Manage the quality assurance department to support the GLP and GMP manufacturing of drug dosage forms for preclinical and clinical trial studies, and commercial production. Frontage Laboratories Inc. is an award winning, publicly listed (HKSE), full-service CRO/Contract Research Organization operating over 25 state-of-the-art laboratories across the US, Canada and China, and growing over 30% YOY. Our core competencies include drug metabolism, pharmacokinetics/ pharmacodynamics (PK/PD), safety and toxicology, bioanalytical services, chemistry and manufacturing controls for drug development, and core laboratory services for clinical trials.
Full-timeExpandApply NowActive JobUpdated 2 months ago - UpvoteDownvoteShare Job
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E.g. knowledge of FDA regulations, GMP/GLP/GCP, Lean Manufacturing, Six-Sigma, etc. e.g. knowledge of FDA regulations, GMP/GLP/GCP, Lean Manufacturing, Six-Sigma, etc. The Sr IT Security Analyst participates in the design, implementation, and maintenance of controls and IT Security practices/procedures to protect company assets.
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Experience with Microsoft Azure and Active Directory. Audit computer systems, network infrastructure and application security in accordance with best practices, applicable laws, regulations and IT security policy.
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Familiarity with GMP/GLP. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products, as well as providing innovative clinical diagnostic testing services, as one of the leading global emerging players in specialised clinical diagnostics testing.
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This role would report into the design and manufacturing arm of analytical instruments. The Manufacturing Technician will play a crucial role in our manufacturing operations, with primary responsibilities including instrument assembly and testing.
$55,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Knowledge of GMP/GLP/GDP. Familiarity with analytical methods including cSDS, cIEF, HPLC, UV-Vis, slope spectroscopy. Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable.
Full-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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At least 1 year of Development or GLP bioanalytical testing experience and 2 years of hands-on experience with (U)HPLC-MS techniques. Proficiency in Sciex, Agilent, or Waters platforms is desirable, with intuitive knowledge across other analytical platforms like HPLC preferred.
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Learn and apply regulatory requirements; HIPAA, GLP, GCP, 21CFR Part 11. Resolian is a Contract Research Organization (CRO) specializing in Drug Metabolism and Pharmacokinetic (DMPK) and bioanalytical services for both small and large molecules.
Full-timeExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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Demonstrated knowledge of GLP and GMP requirements. Expertise in biochemical, biophysical and/or analytical methodologies such as HPLC, spectroscopy (e.g. UV, IR, Raman), light scattering (e.g. SLS, DLS), particle analyzers (e.g. MFI, HIAC), and separation methods (e.g. CEX, cIEF, HIC.
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Perform analytical, mechanical, and biochemical assay testing, as well as polymer synthesis, polymer processing, natural materials manufacturing and characterization, according to dsm-firmenich Quality Systems protocols for raw materials, intermediates, and finished products while maintaining a laboratory notebook and other associated documents.
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The Analytical Chemist will perform analytical testing of pharmaceutical samples in accordance with customer methods, Catalent Micron procedures/policies and cGMPs∯*∯ Rigorous documentation of all testing activities is required, including the maintenance of laboratory notebooks, preparation of detailed laboratory reports, investigation reports etc.
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