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Works closely with Director, Sample Management and Lab Support, and Central Lab leadership to ensure employee engagement, department alignment and agility, and to establish and improve processes.
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Perform high-volume ICP-MS sample analysis and/or data analysis, data QC, and data interpretation. ICP-MS Scientist / Bioanalytical Services. Perform high-volume ICP-MS sample analysis and/or data analysis, data QC, and data interpretation.
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In this role you will collaborate with Assay Automation, Integration Automation, Assay Development SMEs, and end-users to increase sample testing throughput and/or reduce hands-on time, time-to-result, repetitive strain, and assay variability.
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Drive the integration of LIMS, sample batching software, and materials inventory systems with laboratory orchestration and scheduler software. Janssen Research & Development, LLC, a division of Johnson & Johnson’s Family of Companies is recruiting for a Lab Automation Engineer to develop and implement fully automated analytics for cell therapy product development and QC. This position will be located in Malvern, PA.
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The candidate will provide leadership in biomarker assay development, implementation and sample analysis. Broad knowledge and in-depth experience in biomarker assay method development, qualification/validation and sample analysis in support of preclinical or clinical studies.
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Position Summary: Performs routine and non-routine microbiology sample analysis (Bioburden, Endotoxin, Environmental Monitoring, Sterility, etc.) Frontage’s core competencies include drug metabolism, pharmokinetics/ pharmacodynamics (PK/PD), safety and toxicology, bioanalytical services, chemistry and manufacturing controls for drug development, and core laboratory services for clinical trials.
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Responsible for data entry, data management, compilation and reporting activities within the Diagnostics group including: clinical and non-clinical sample biorepositories, coordination for sample reconciliation, shipping, compilation and maintenance of sample and data/assay tracking sheets.
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Marken offers a state-of-the-art GMP-compliant depot network and logistic hubs for clinical drug product storage and distribution worldwide, and supports cell and gene therapy logistics services from clinical to commercial, while maintaining the leading position for Direct-to-Patient and Home Healthcare services, biological sample shipments and biological kit production.
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Applications must include a resume, law school transcript, references, and writing sample. The company is seeking a mid-level litigation associate to join its Complex Litigation Practice Group.
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Maintain Laboratory Housekeeping including: sample management, reagent prep, instrument standardization/calibration. One of our large pharmaceutical clients is seeking to bring on a QC Analyst II to join their growing 3rd shift team in Malvern, PA. The QC Analyst position supports the Quality Control In-Process and conducts biochemical, microbiological, and general chemical testing of in-process or final product samples submitted to the QC laboratories.
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In this role, you will report to Supervisor, Onsite Services and will work closely with the Avantor's Lab and Production Services team of over 1,500 on- and off-site expert personnel - and our customers - to perform customized, mission-based lab work and research protocols that help return time back to science.
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Prepare samples for sample testing through dilution and other techniques. Preform qualifications and validations utilizing cutting edge instrumentation such as cSDS, cIEF, HPLC, UV-Vis, slope spectroscopy.
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Independently design and develop methods, and complete complex lab work, sample analysis, validation, and method development. Knowledge and understanding of regulatory requirements; GLP, GCP, 21CFR Part 11, GDP, GMP.
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Performs routine sample analysis, and a variety of tasks to support product development, ensuring agreed timelines. Hands-on experience with HPLC, UPLC, GC, LC/MS, IC, and Dissolution Testing. Complies with all relevant cGMP, and/or GLP regulatory requirements while carrying out assigned studies.
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Monitors and maintains medication sample closet. Train back-office staff on an as needed basis when requested by Office Administrator. Monitors and maintains medication sample closet. Completes the referral process on specific procedures when requested to do so by Office Administrator.
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