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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.
$26 an hourFull-timeExpandApply NowActive JobUpdated 12 days ago - UpvoteDownvoteShare Job
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Oversee GLP and non-GLP in vivo (e.g. rodent and non-human primate) studies internally or out-sourced from lead selection screening through lead candidate IND-enabling work. We provide equal employment opportunities to all applicants for employment and existing employees without regard to ancestry, national origin, place of birth, race, color, gender, sexual orientation, marital status, pregnancy, religion, age, disability, gender identity, results of genetic testing, service in the military or otherwise to the full extent of all federal, state and local laws.
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Provide strategic leadership in defining the vision, framework, and requirements for the R&D archival program, working across the global enterprise with key stakeholders (e.g., in Research, Global Quality, Pharmaceutical Sciences, Plasma-Derived Therapies) to implement, as well as ensure execution and compliance to Takeda standards and global Good Laboratory Practice (GLP) regulations [e.g., 21 CFR Part 58; OECD (Organization for Economic Co-operation & Development) Principles of GLP.
$266,200 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Lead identification of assay requirements, lab selection, and contract development to ensure regulatory compliance according to GLP, GCP, and applicable global regulatory requirements such as CLIA and EU IVDR, and execution feasibility.
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The incumbent is a self-directed clinical exercise physiologist with strong clinical skills and experience in applied cardiopulmonary exercise testing (metabolic gas exchange). QualificationsSKILLS/ABILITIES/COMPETENCIES REQUIRED:The exercise physiologist will be expected to have: Proficiency in the performance of cardiopulmonary exercise testingPossess communication skills necessary to explain exercise or physiological testing procedures to patients while inspiring confidence and motivation for patients.
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Screen excipients/formulation vehicles for solubility and stability to optimize preclinical formulations to enable non-GLP and GLP pre-clinical studies. Execution of analytical experiments with XRPD, DSC, TGA, DVS, SEM, optical microscopy and UPLC/HPLC (Empower.
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Review and evaluate immunoassay bioanalytical results supplied by external CROs to ensure quality; review GLP and clinical BA assay validation protocols and reports. Review and edit GLP and clinical BA assay validation protocols, and reports.
Full-timeExpandApply NowActive JobUpdated 15 days ago - UpvoteDownvoteShare Job
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Protein characterization by analytical SEC, gel electrophoresis, nanodrop and endotoxin testing. DNA characterization and quality control testing using techniques such as gel electrophoresis, RNaseA testing, nanodrop, PCR, and preparation of samples for sequencing analysis (Sanger and NGS.
$58.62 an hourExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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O Oversee execution testing of Security Incident Event Management (SIEM) across several security domains including Cloud SaaS vendor, Comptroller’s office, and EOTSS. o Oversee integration testing of EOTSS Single Sign On (SSO), EOTSS Identify Access Management (IAM), EOTSS Multi-Factor Authentication (MFA), Cloud SaaS Vendor user access management, and Comptroller’s access controls and provisioning processes.
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B.S. degree in chemistry, analytical chemistry, pharmaceutics, chemical engineering or material sciences. An ideal candidate will have a strong foundation in analytical techniques such as UPLC/HPLC (Empower proficiency) and an understanding of early drug development processes and experiments.
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Skills & Requirements:B.S. degree in chemistry, analytical chemistry, pharmaceutics, chemical engineering or material sciences. An ideal candidate would have approximately 2+ years' experience working in pharmaceutical sciences (preformulation, analytical or formulation development.
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Systems include but are not limited to EPIC, Optility, PET Manager, Syngo, and ·Alerts Unit Technical/Operations Manager regarding equipment problems, problems encountered during testing, etc. ·Follows the instructions of the Authorized User (AU) physician and authorized nuclear pharmacist for the preparation of radiopharmaceuticals and quality control testing.
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5 years of experience black-box, white-box, functional, smoke, and regression testing. Familiarity of testing types: black-box, white-box, functional, smoke, and regression. Strong experience in Test Automation and EDI, HIPAA, PHI and NCPDP Testing.
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Keeps current regarding development in technical instrumentation to trends and techniques in cardiac ultrasound testing through appropriate journals and attends seminars and other meetings per approval of echo supervisor.
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Responsible for Quality & Controls Assurance programs, activities and reviews, including claims reviews; call center and digital communications reviews; Medicare Risk Adjustment, HCC, clinical and coding reviews; DRG and medical records reviews; technology/systems and coding upgrade and implementation reviews (e.g. final user acceptance testing, etc.
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glp testing jobs Title: analytical in Boston, MA
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