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Lean Six Sigma Green Belt certification is a plusExperience with Agile configuration product management software - preferredExperience with Oracle and DataSweep or other electronic device history record system - preferredExperience working in a manufacturing and/or laboratory environmentGood written and verbal communication skillsSkills/Abilities:Ability to work independently as well as within a team of professionals.
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Conduct Quality Control Analytical testing (e.g., ELISA, Flow Cytometry, PCR) of patient samples, stability samples, controls, and reagent qualification in a GMP environment. Conduct Quality Control Analtyical testing (e.g., ELISA, Flow Cytometry, PCR) of patient samples, stability samples, controls, and reagent qualification in a GMP environment.
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Skills: FDA, MS-WORD, MS-EXCEL, MS-Powerpoint, Laboratory Information Management Systems (LIMS), GMP (Good Manufacturing Practice) - Individual should have knowledge of current Good Manufacturing Practices (cGMP), Laboratory Information Management System (LIMS), Microsoft Office™ applications specifically Word and Excel, analytical techniques and instrumentation, Lean Six Sigma concepts, and Lean Labs.
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Familiar knowledge of GLP and GMP requirements as they pertain to protein and gene therapy process development and Quality Control (QC) testing is a plus. Leads the laboratory-based analysis of the physico-chemical and biological properties of proteins and gene therapy vectors and establishes the laboratory standards to determine identity, strength, purity, potency and quality for research and development candidates.
$125,700 - $182,250 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Analytical laboratory experience in a GLP/GMP regulated environment is preferred. The Chemistry Supervisor will lead tech transfer activities of qualified analytical methods from a designated donor laboratory.
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Performs general laboratory support activities including reagent preparation, sample management, equipment maintenance, lab housekeeping etc. skills: Quality control, HPLC, SOP, Chemistry, GMP (Good Manufacturing Practice.
$30 - $37.16 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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With analytical techniques, such as QPCR, PCR, SDS-PAGE, Western blotting and ELISA - Exp. with electronic laboratory notebook applications, such as Benchling - Basic knowledge and application of theories, principles and techniques in molecular biology and cell biology "Nice to Haves": - Experience in a QC/GMP testing environment a plus Duties/Responsibilities: - Operate and maintain standard laboratory equipment and department-specific equipment.
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The Senior Clinical Laboratory Scientist role performs laboratory testing procedures and laboratory management in a safe and effective manner resulting in quality cell product collections for optimal patient outcomes.
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Facilities Maintenance activities, including budget, schedule, and document management, in the design, cost estimating, procurement, installation, construction, modification, and commissioning, as applicable, of complex multi-system, multi-discipline equipment and systems for general use and GMP regulated areas.
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Knowledge of Good Clinical practice (GCP), Good pharmacovigilance Practice (GVP), Good Manufacturing Practices (GMP), Good Documentation Practices (GDP), and Good Laboratory Practices (GLP.
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The Sr. Validation Specialist is responsible for compliance oversight of enterprise CSV projects as part of the IT team. Coordinates and/or supports delivery of compliance deliverables such as System Inventory, Quality Impact Assessments, Data Integrity Assessment, Risk Assessments, Gap Analysis, System Remediation, System Change Control and CAPA.
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Maintain a laboratory notebook and other technical documentation according to required GLP/GMP guidelines. BS in Chemical Engineering, Polymer Engineering, Material Science, Biomedical Engineering, Mechanical Engineering, or related scientific discipline with 4+ years of product development experience is required.
$60,000 - $160,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Pcr, microbiology, bacteriology, laboratory, biology, gmp, microbiology laboratory, microbiological, aseptic technique, bioburden, media, Receive in and track isolates using electronic laboratory.
$19.25 - $22 an hourFull-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Will need to follow Standard Operating Procedures, Good Laboratory Practices (GLP), and Good Manufacturing Practices (GMP). Hands on laboratory ab experience from coursework, undergraduate research, or internship.
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We're looking for a dynamic Chemical Engineer to lead projects ranging from $50K to $1M, including site expansions, laboratory enhancements, equipment updates, and utility improvements. Join a leading innovator in the production of high-purity GMP chemicals, where your expertise can shine and grow.
$100,000 - $130,000 a yearFull-timeExpandApply NowActive JobUpdated Today
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