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The QC Reviewer is responsible for compliance with Standard Operating Procedures (SOP) and Good Laboratory Practice (GLP) requirements at Pharma Medica Research Inc (PMRI), as well as raw date verifications, preparation of analytical reports and maintenance of laboratory log sheets/books.
ExpandApply NowActive JobUpdated 13 days ago - UpvoteDownvoteShare Job
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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.
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Or in a Clinical Development role with expertise and/or transferable skills related to Good Clinical Practice (GCP), and/or Good Pharmacovigilance Practice (GVP). The GDQIM team is tasked with effective planning, preparation, conduct and follow-up of GCP, GVP and GLP inspections conducted by regulatory authorities.
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Can streamline research by delivering operational and cost efficiencies through the strategic insourcing of GMP, GLP and non-GLP research services from discovery through safety assessment.
Full-timeExpandApply NowActive JobUpdated 17 days ago - UpvoteDownvoteShare Job
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The QC Analyst Lead Microbiology provides essential support to manufacturing by leading in conjunction with the Laboratory Supervisor, with a deep understanding of environmental monitoring principles and laboratory testing, including Endotoxin, Mycoplasma, Sterility, and growth promotion, the Lead Analyst serves as a backup to the supervisor, performs qualification testing, trains staff, manages supplies, reviews data accurately, and contributes to data analysis and reporting.
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Maintains consistent practice of general company and safety policies and procedures and MSDS guidelines, including those related to biohazards and radioactive substances. The Corporate Functions provide operational support across Charles River in areas such as Human Resources, Finance, IT, Legal, Sales, Quality Assurance, Marketing, and Corporate Development.
ExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Experience in a research/lab animal/GLP environment. Ability to practice veterinary medicine in the work state highly desirable. Licensure to practice veterinary medicine in at least one U.S. state.
$145,000 - $165,000 a yearFull-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Certification/Licensure: Licensure to practice veterinary medicine in at least one U.S. state required. Knowledge of laws, regulations, policies and guidelines that govern animal research, research conduct principles and current methodology of laboratory animal medicine and management required.
$160,000 - $170,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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To achieve goals Ability to drive progress and deliver results o multiple priorities, projects, and timelines concurrently Follow all Good Manufacturing Practice (GMP) and Good Laboratory Practice (GLP) guidelines and assist in enforcing policies throughout the organization This role may require travel to manufacturing plants (<20%) Participate in training and onboarding initiatives as needed and lead training for any direct reports.
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Fundamental to basic research and discovery is the use of in vivo models to help identify disease targets and determine potential biological pathways that regulate the condition. We are seeking an Animal Support Technician in our GEMS Department for our site in Wilmington, MA.
$18 an hourExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Charles River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art facilities and expert regulatory guidance. Charles River Laboratories is an Equal Opportunity Employer - M/F/Disabled/Vet.
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Certification/Licensure: Current license to practice veterinary medicine in at least one state. Other: ACLAM Diplomate Status preferred. Serve as a member of the Site Management Team and site representative of the Global Safety Assessment Veterinary Medicine Functional Matrix.
$200,000 - $250,000 a yearFull-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Maintain SOPs for review and approval by Capability Area Manager and monitors compliance with DoD/Army safety procedures and Good Laboratory Practice (GLP), Clinical Laboratory Improvement Amendments (CLIA), Clinical Laboratory Improvement Program (CLIP), and the College of American Pathologist (CAP) regulations.
Full-timeExpandApply NowActive JobUpdated 21 days ago - UpvoteDownvoteShare Job
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Build, train, and develop highly skilled production teams capable of producing cell therapy products in accordance with regulatory guidelines and Cognate quality standards. Offering a variety of services such as contamination and impurity testing, protein characterization, bioassays, viral clearance studies and stability and lot release programs, we support clients throughout the biologic development cycle, from the establishment and characterization of cell banks through preclinical and clinical studies to marketed products.
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Demonstrates a thorough knowledge of Good Clinical Practice GCP, Good Pharmacovigilance Practices GVP, Good Laboratory Practice GLP, Good Documentation Practice GDP and ICH E6 R2 compliance requirements.
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