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The ideal candidate is well-versed in oligonucleotide synthesis and purification techniques, analytical and production instrumentation, and experienced in GLP/GMP documentation (NCRs, CAPAs, CHGs, protocol, and report writing.
$130,000 a yearFull-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Authors assay qualification protocols and bioanalytical reports for non-GLP tox studies. · Supports outsourced bioanalytical activities, providing assay reagents, CoAs and other GLP related documents.
$120,000 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Experience in GLP/GMP Manufacturing Procedure and Documentation. Experience in Organic Synthesis, Polymer Chemistry, Raw Material Management, Materials Testing. Experience in GLP/GMP Manufacturing Procedure and Documentation.
ExpandApply NowActive JobUpdated 20 days ago - UpvoteDownvoteShare Job
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Familiar with regulatory standards and quality systems (e.g., GLP, GMP). Maintain thorough and accurate records of laboratory work. Extensive hands-on experience in a wide range of analytical techniques, such as UV-Vis, HPLC, CE, SDS-PAGE, icIEF, LCMS, GCMS, enzyme kinetics, colorimetric and fluorescent plate-based assays, ELISA, Western Blot, etc.
$170,000 a yearFull-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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PhD in Analytical Chemistry, Chemistry, Biochemistry, or related discipline, OR MS in Analytical Chemistry, Chemistry, Biochemistry, or related discipline with 3+ years of experience in an cGMP or GLP analytical laboratory environment, OR BS in Analytical Chemistry, Chemistry, Biochemistry, or related discipline with 5+ years of experience in an cGMP or GLP analytical laboratory environment.
$135,000 a yearFull-timeExpandApply NowActive JobUpdated 22 days ago - UpvoteDownvoteShare Job
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Comprehensive knowledge of GLP regulations, including previous GLP experience in pharmaceutical or biotechnology industry or equivalent GXP transferable experience. Oversee and provide strategic direction for Toxicology/Pathology, BioAnalytical/DMPK, Biomarkers, and Clinical Pharmacology teams to ensure robust support for clinical development programs.
$300,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Strong knowledge of global regulatory requirements of GMP, GCP, GLP, GDP and/or other domains. Broad understanding of the development and test management tools, including experience with HP ALM, Jira, and Azure DevOps.
$199,320 a yearExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Knowledge of FDA regulations, ICH Guidelines, GCP and GLP, and familiarity with standard clinical operating procedures is a plus. Clinical Project Assistant (CPA) – Biomarker & Bioanalytical.
$45 an hourExpandApply NowActive JobUpdated 18 days ago - UpvoteDownvoteShare Job
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Assists with tracking and shipping of biomarker & bioanalytical samples and sample reconciliation across projects. Provides support and assistance to the biomarker & bioanalytical operations team. May serve as a resource within Clinical Operations for clinical trial systems used for managing clinical trials and publications.
Full-timeExpandApply NowActive JobUpdated 22 days ago - UpvoteDownvoteShare Job
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This position requires a senior-level individual with 10+ years of experience in supporting computer system validation (CSV) efforts for infrastructure and applications used in GMP, GLP and/or GCP processes.
ExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Ensures that personnel, methods, corporate policies and standard operating procedures comply with: FDA requirements for Good Laboratory Practices (GLP) for conducting scientific research, current Good Manufacturing Practice (cGMP), Quality System Regulation (QSR), Good Clinical Practices (GCP), and 21 CFR Part 11.
Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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May ensure compliance to in-house and/or external specifications and standards, (i.e. GLP, GMP, ISO, Six Sigma) Internal Collaborations – Manufacturing, Quality Control, Quality Operations, Process Development, Analytical Development, Supply Chain, Regulatory Affairs, Alliance Management, among others.
Full-timeExpandApply NowActive JobUpdated 17 days ago - UpvoteDownvoteShare Job
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A solid understanding of GCP, GLP, GMPs and CMC requirements is expected. In depth knowledge of regulations and guidance supporting GCP and GLP to include FDA, EMA, ISO standards and ICH guidelines with direct impact to clinical programs.
$230,000 a yearFull-timeRemoteExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Advanced leadership skills and a partnership mindset, anchored by expert knowledge of the regulations governing preclinical research, drug development and post marketing activities (i.e., GCP, GLP/GCLP, and GVP), as well as a keen understanding of process controls will enable success in this role.
$323,070 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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A current California Clinical Laboratory Scientist License that meets requirements for Testing Personnel under CLIA regulations (42 CFR, part 493) (ASCP, CGMBS, or Generalist license is required.
$150,000 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago
glp job Title: laboratory assistant in Foster City, CA
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