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In January 2020, HemaCare was acquired by Charles River Laboratories, an early-stage contract research organization (CRO). HemaCare’s vertically integrated solutions support preclinical research, clinical studies from phases 1 to 3, and commercialization with high-quality RUO and GMP-compliant starting material and apheresis collections.
$39.86 - $49.23ExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Initiate deviations or investigations of multiple complexities and work with cross-functional departments to identify root causeImplement appropriate corrective actions, assist with investigations, complete action items for GMP investigations and CAPA's and revise and author Standard Operating Procedures/Batch Records.
$42.31 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Reporting to the Director, QC Molecular Biology, the Analyst I - QC Molecular Biology will support the gene therapy program pipeline including but not limited to routine GMP testing of AAV vector analytical methods such as GC titer determination by ddPCR and qPCR, impurity testing, and other methods as needed.
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Basic Qualifications Requires 3-5 years with a BS degree in a related scientific discipline ( chemistry, biology) or equivalent combination of education and previous relevant experience in the pharmaceutical industry, related GMP environment, or equivalent.
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Work under the Production Department director to support production by performing GMP radiochemistry processes in a safe, efficient and timely manner. Currently they are looking to add another GMP Production Chemist to join there happy & growing team.
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Typically requires 3-5 years with a BS degree in a related scientific discipline (e.g. chemistry, biology) or equivalent combination of education and previous relevant experience in the pharmaceutical industry, related GMP environment, or equivalent.
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Be observant for employee safety in addition to GMP compliance and make immediate corrections to GMP discrepancies as needed and report them to the supervisor/manager. The individual will be responsible for running a balance of the following functions: production, machine repair/trouble shooting, and assist the Production Manager as needed.
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We provide process development, produce GMP viral vectors, and provide cell transduction for gene and cell therapy clinical trials and are proud to be a part of the process that leads to new cures.
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Applies advanced working knowledge and experience to independently improve maintenance techniques and operations in a highly regulated GMP environment under the guidance and direction of the Maintenance & Facilities Manager.
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Comply with Good Manufacturing Practices (GMP), sanitation procedures and general housekeeping as well as all safety practices and procedures. Knowledge and understanding of Good Manufacturing Practices (GMP.
$34.9 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The role involves leading a team of senior engineers, managing the validation strategy, and ensuring compliance with GMP standards for a combination product that involves filling a hydrogen peroxide solution into vials.
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Understanding of GMP/GDP compliance requirements; understanding of FDA and Global GMP Quality Requirements. Conduct GMP external audits of Sarepta approved vendors including Contract Manufacturers, APIs, Drug Product, Primary and Secondary Packaging, Contract Laboratories, 3PL and transport vendors.
$165,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Skills:Inspection, GMP, Clean Room, Packaging, Quality Assurance Experience:Entry Level1 year(s) responsibilities: Responsible for the labeling and packaging of pharmaceuticals for world wide distribution.
$23.5 - $24 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Candidates for this role need to be detail oriented, a strong communicator with GMP and quality documentation experience (reviewing, editing, managing). We’re looking for someone with 8 months to 2 years’ experience in a GMP manufacturing environment.
$32 an hourExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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Demonstrated understanding FDA/ICH GMP/GCP/GLP/GDP requirements and practices, ability to apply and educate team members and cross-functional partners. Demonstrated understanding FDA/ICH GMP/GCP/GLP/GDP requirements and practices, ability to apply and educate team members and cross-functional partners.
$195,000 a yearFull-timeExpandApply NowActive JobUpdated 14 days ago
gmp job Company: Charles River Laboratories in Wilmington, MA
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