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12+ years' work experience in the biologics industry, preferably in a laboratory setting. Experience working in a regulated clinical laboratory (CLIA /CAP/ FDA / ISO). This position is eligible for benefits including but not limited to medical, dental, vision, life insurance, disability coverage, flexible paid time off, Spring Health, Carrot Fertility, participation in a 401k with company match, ESPP, and many other additional voluntary benefits.
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Combining unlimited computation and storage with powerful tools for data sharing, visualization and analysis in a customizable development platform, Orion offers unprecedented capabilities for the advancement of pharmaceuticals, biologics, agrochemicals, and flavors and fragrances.
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One (1) year work experience in biologics quality assurance preferred. We are seeking a Quality Assurance Technician to join our growing biopharmaceutical company and assist in opening our newest Donor Center.
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We are a leading global spine and orthopedics company with a premier portfolio of biologics, innovative spinal hardware, bone growth therapies, specialized orthopedic solutions and a leading surgical navigation system.
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A minimum of 5 years' experience in a pharmaceutical/biologics company with at least two (2) in third party manufacturing QA. Experience with biologics/vaccines is required. The Manager/Senior Manager of Quality Assurance provides oversight of GMP activities for Quality Control Release and Stability testing including method validation and transfer.
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We serve some of the best-known companies and work with many of the most advanced drugs, biologics, and medical devices in development today. Perform tracking of out-of-scope services on assigned projects, provide cost estimates, and draft change orders to existing service work orders.
Full-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Just-Evotec Biologics is seeking a motivated and creative Scientist II who desires a significant opportunity to improve worldwide access to biotherapeutics. As a key member of the analytical development group, the successful candidate will have understanding of immunoassay and qPCR method development and qualification/validation, as well as strong experimental design and data analysis skills.
Full-timeExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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Knowledge of ELN/LIMS (Benchling), PreClinical LIMS (Ascentos), Genedata Biologics. The ideal candidate will possess business acumen and technical background in a hybrid GxP environment, encompassing both on-premises and AWS infrastructure, as well as a good understanding of Drug Discovery and Development needs within the BioPharma industry.
$130,220 - $168,520Full-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Ph. D. in a relevant scientific area, such as protein sciences, protein biochemistry, or biotechnology, plus a minimum of 7 years of professional experience in biologics research and/or development required.
$158,500 - $192,900 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Turnstone Biologics is a clinical-stage biotechnology company developing new medicines to treat and cure solid tumors by pioneering a differentiated approach to TIL therapy. Turnstone Biologics is seeking a driven and experienced Sr. Process Engineer/ Principal Specialist to support the Manufacturing Science & Technology Team (MSAT.
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We are seeking a Director for our Market Access Strategy in the Biopharmaceuticals Business Unit. This role is a key step on your journey to becoming a future leader at AstraZeneca, where you will learn how the enterprise runs, what it takes to succeed, and what excellence in Commercial looks like.
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Knowledge of biologics regulatory guidelines including FDA/ICH on risk management, technology transfer and process validation. Development of robust, scalable, well characterized and cost-effective downstream processes for the biologics pipeline.
$160,000 - $200,000 a yearExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Deliver outcomes focused on the management and utilization of data to transform the speed of biologics discovery & development as part of the Biologics NExT initiative. Experience with bioinformatics applications including NGS pipeline development.
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Compounds IV admixtures, chemotherapy, desensitization medications, high-cost biologics and pediatric IV’s and restocks CPR cart trays. Adds patient specific and re-stock medications to the Omnicell machines located in patient care areas, except the sterile corridor of surgery.
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Be an advocate and Subject Matter Expert for the AGC Biologics CAPEX Delivery Process (CDP) Because of our dedication to building and empowering our internal teams, AGC Biologics is an innovative leader in the industry with an extensive network of cGMP facilities in the US, Europe and Asia. As such, we deliver a deep expertise, dynamic solutions and technologies, as well as customized services for the scale-up and cGMP manufacturing of protein-based therapeutics.
$124,320 - $170,940 a yearFull-timeExpandApply NowActive JobUpdated 6 days ago
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