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Bachelor’s degree in biological science(s) field or related engineering with: For BMA I’s, 0-2 years of experience in cGMP biotech manufacturing, preferably cell and gene therapies. The incumbent will ultimately perform routine cGMP manufacture of multiple cell and gene therapy types/products at our state-of-the-art BaseCamp facility such as CAR-Ts, iPSCs, Adeno-Associated Virus (AVV) and Lentivirus (LV.
Full-timeExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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Quality Control and/or Analytical Development experience in Biotech, cGMP areas. Experience in gene therapy cGMP manufacturing and testing. The Senior QC Analyst position interacts regularly with TScans Quality Assurance, Analytical Development, Process Development, Manufacturing, Facilities, as well as TScans external test laboratories, where applicable.
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Support cGMP manufacturing and technology transfer to large-scale peptide production facilities. Amgen is seeking a dedicated Process Development Senior Principal Scientist with industry experience in peptide synthesis and manufacturing to join our Drug Substance Technologies - Synthetics (DSTS) group in Cambridge, MA. Amgens DSTS group within Process Development (PD) is responsible for the invention, development, and implementation of drug substance manufacturing processes and technologies to advance Amgen's portfolio of synthetic and hybrid assets.
Full-timeExpandApply NowActive JobUpdated 21 days ago - UpvoteDownvoteShare Job
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This position performs laboratory scale development activities for the purification of pre-clinical and cGMP grade rAAV vectors. Job Title: Associate Scientist II, Downstream Process Development (Contract.
ExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Strong cGMP skills. Performs Bio-Analytical testing such as Flow Cytometry, ELISA, qPCR, cell count, (incoming, in-process and final product release testing). TScan's discovery platform is centered around a breakthrough technology that enables the rapid, comprehensive, and genome-wide identification of the peptide antigen targets of T cell receptors.
ExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Support cGMP manufacturing and technology transfer to our internal manufacturing facilities and external contract manufacturers. M.S. in organic chemistry or biochemistry/chemical biology with a specialization in synthetic methodology, total synthesis, peptide/protein chemistry, oligonucleotide chemistry, or synthetic/conjugation chemistry.
$82,396 - $99,167 a yearFull-timeExpandUpdated 23 days ago - UpvoteDownvoteShare Job
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Develop & provide cGMP & GDP SOP training in interface within global Pharm Dev QMS to support particularly clinical supply chain teams. Oversee generation and review of documents used in cGMP & GDP activities such as Quality Agreements.
ExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Doctorate degree in organic chemistry or biochemistry with a specialization in biocatalysis, oligonucleotide chemistry, synthetic/conjugation chemistry and/or chemoinformatics/machine learning. Amgen is currently seeking a talented Process Development Senior Scientist to join our Drug Substance Technologies - Synthetics (DSTS) group at Cambridge, MA. Amgen's DSTS group within Process Development (PD) is responsible for the invention and development of drug substance manufacturing processes and technologies to advance Amgen's exciting portfolio of synthetic and hybrid assets.
Full-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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To accomplish this, we continue to be deeply rooted in science and academic research while also having built a fully integrated, global immunotherapy company with cGMP and GMP manufacturing facilities anchored around deep expertise in immunology and complemented by an expanding set of capabilities.
Full-timeExpandUpdated 10 days ago - UpvoteDownvoteShare Job
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Routinely provide performance feedback and guidance to employees in addition to conducting formal evaluations and reviews QUALIFICATIONS BS or MS in analytical chemistry, biochemistry, or biotechnology or equivalence BS with 3+ years or MS (0+ years) of professional experience in the vaccine or pharmaceutical industry in the field of QC analytics or R&D. Preferred 2 years of experience in cGLP or cGMP lab.
ExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Experience managing external CMO’s and working in a regulated cGMP environment, with knowledge of cGMP/ICH/FDA/EU regulations. 10+ years of experience in biologics process development with a strong understanding of antibody processing, including upstream and downstream processes.
ExpandApply NowActive JobUpdated 12 days ago - UpvoteDownvoteShare Job
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Expertise with biologics cGMP manufacturing, with experience in cell and gene therapy preferred. This leader and the team will need to coordinate cross-functionally with Process and Analytical Development, Internal and External Manufacturing, Validation and Metrology, Quality Control and Analytical Technologies (QCAT), Quality Assurance, and Regulatory to support process validation and manufacturing of gene editing components and ex vivo CRISPR gene-edited cell therapies both internally and at Contract Manufacturing Organizations (CMOs.
Full-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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CGMP Experience preferredERP/MRP experience required with Syteline experience preferred Physical Demands: Position requires the ability to lift and move heavy objects. Align with demand planner, supply planner, inventory planner, and buyer in the planning and execution of the supply chain components of product strategy in support of the program goals and KPIs. What We’ll Expect From You: Skill and Knowledge Requirements: Excellent organizational, record keeping and communication skills.
Full-timeExpandUpdated 1 month ago - UpvoteDownvoteShare Job
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Thorough understanding of drug development and commercialization process including strong knowledge of cGMP US and EU regulations/clean room experience. Serve as QA lead for quality system elements including Document Control, Training, Deviation Management, Internal and External Inspection, Supplier Management, Risk Management, Complaints, Recalls, etc.
ExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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The Senior Principal Scientist role will include leading a multidisciplinary team of chemists and chemical engineers in the development of efficient and sustainable manufacturing processes for peptide synthesis and purification, driving technology innovation in the areas of chemical and microbial recombinant peptide production technologies, and providing technical expertise as well as developing and mentoring staff within the organization.
ExpandApply NowActive JobUpdated 11 days ago
cgmp job in Lexington, MA
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