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8 years of experience in a facilities role with a focus on HVAC in a regulated manufacturing environment within the biotechnology, pharmaceutical, gene therapy, or cell therapy industry. 8 years of experience in a facilities role with a focus on HVAC in a regulated manufacturing environment within the biotechnology, pharmaceutical, gene therapy, or cell therapy industry.
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Qualifications: Bachelor's degree in Biotechnology, Biochemistry, Molecular Biology, or related field. Perform routine production activities such as upstream and downstream processing, purification, and formulation.
$32 - $34 an hourFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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PhD in organic chemistry, medicinal chemistry, or relateddiscipline with 4+ years of drug discovery in biotechnology or pharmaceutical industry or BSc/MSc in organic chemistry, medicinal chemistry, or relateddiscipline with 10+ years of drug discovery in biotechnology or pharmaceutical industry.
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Department Summary: MITRE Accelerator is seeking a Director Private Sector Collaboration to create the next generation of innovation with different industrial verticals in cybersecurity, digital health, biotechnology, transportation, AI, semiconductors, future connectivity, and climate, energy & environment.
Full-timeExpandApply NowActive JobUpdated 15 days ago - UpvoteDownvoteShare Job
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If you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, please contact a member of our Human Resources team by sending an e-mail message to crrecruitment_US@crl.com.
$18 an hourExpandUpdated 4 days ago - UpvoteDownvoteShare Job
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The company is the leading producer of polypropylene in the United States, with six production plants located in Texas, Pennsylvania, and West Virginia, an Innovation and Technology Center in Pittsburgh, and a New Renewable Innovation Center in Boston focused on leveraging groundbreaking developments in biotechnology and advanced materials.
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IPS, a Berkshire Hathaway Company, is a global leader in developing innovative business solutions for the biotechnology and pharmaceutical industries. Process Architecture, Process Design, Engineering, Construction, Commissioning, Qualification, LEAN Project Delivery, Strategic Master Planning, Energy Conservation Management, Project Controls, Program/Project Management, Operations/Logistics Strategy and Planning, EPCMV and Staffing Services.
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Rapid Micro Biosystems creates, sells, validates, and services innovative products for fast, accurate, and efficient detection of microbial contamination in the manufacture of pharmaceuticals, biologics, biotechnology products, medical devices, and personal care products.
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Lead Root Cause Failure Analysis (RCFA) and Failure Mode Effect Analysis (FMEA) in cGMP, biotechnology environment. Understanding of process improvement and reliability engineering principles, methodologies and tools such as PDCA, LEAN, Six Sigma / DMAIC, FMEA is desirable.
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The incumbent should have 5-10 years of experience in the biotechnology or pharmaceutical industry. Knowledge of protein characterization techniques such as SDS-PAGE, Western blot, Octet, UV Vis, and analytical SEC is a plus.
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5- 7 years of industry experience in immunoassay development, life science, biotechnology, or IVD markets. Experience in immunoassay product development strongly desired, including: reagent development and optimization, assay protocol optimization, migration of manual assays to automated instrumentation, specifications development, statistical methods, verification and validation protocol writing and execution, conformance with design control regulations.
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Alexion- Astrazeneca rare disease Gemonics Medicine department is seeking a highly motivated Co-op to join our gene therapy and molecular cloning group.
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Embrace a thrilling opportunity to work with a leading biotechnology company that is revolutionizing healthcare through groundbreaking mRNA technology. Aptitude or ability to learn to gain a strong understanding of GxP regulations (specify GMP, GLP, GCP, GVP or other applicable standards.
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Minimum of 3 years relevant laboratory experience in a contract research organization (CRO), biotechnology, or pharmaceutical Minimum of 2 years of management experience, including staff management and developmentExpertise in Bioanalysis and in the design, conduct, and interpretation of in vivo PK studies isExperience with noncompartmental analysis (Phoenix WinNonlin) is required.
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Requirements: Bachelor’s degree in Biotechnology, Supply Chain, Engineering or related STEM discipline, Masters desired. Position Summary:ultrafocused – Work together to fearlessly uncover new possibilitiesReporting to the Head of Global Planning, Ultragenyx is seeking a highly motivated Associate Director, Clinical Supply Gene Therapy with expertise in end-to-end pharmaceutical clinical supply strategies and operations.
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biotechnology job Company: Charles River Laboratories in Wilmington, MA
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