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They will collaborate with various internal functions including Analytical, Upstream/Downstream Manufacturing, Quality Control, Quality Assurance, Regulatory, and Supply Chain to ensure best practices are implemented and followed at external contract manufacturing and testing labs, and internally at Leap Therapeutics.
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Drive standardization and implement process improvements, efficiencies and automation across the AP function with upstream and downstream processes. Work with Accounts Payable Manager to deliver Internal / External Auditors for Sox compliance requests, substantive testing and quarterly / annual audit preparation.
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Demonstrated knowledge of cGMP manufacturing with knowledge in manufacturing operations in downstream processing utilizing single use technology (SUT). Demonstrated knowledge of cGMP manufacturing with knowledge in manufacturing operations in downstream processing utilizing single use technology (SUT.
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Downstream experience with standard chromatography and/or DNA purification kits is a plus. The Research Production team is responsible for the upstream enzymatic synthesis and downstream manufacturing of drug substance to support pre-clinical trials.
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Develop data strategy that enables the whole business to operate and shows downstream impacts of learning on business growth and product adoption. 13 years of experience using analytics to solve product or business problems, performing statistical analysis, and coding (e.g., Python, R, SQL), or 10 years of experience with a Master's degree.
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Effectively identify, adjust for and communicate downstream impacts of project changes. Bright Horizons complies with the laws and regulations set forth in the following EEO is the Law Poster: EEO English ( and EEO Spanish ( along with information on the Family and Medical Leave Act (FMLA) ( and Employee Polygraph Protection Act (EPPA.
Full-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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In coordination with Blueprint's upstream and downstream trading partners, ensure U.S. serialization compliance requirements for Blueprint's commercial products are met. The Manager, Packaging Engineer will provide technical expertise associated with pharmaceutical packaging and serialization programs for Blueprint Medicine's clinical and commercial products, including packaging design and specification, equipment/tooling design, qualification and validation, artwork & labeling, material selection and testing.
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Solid knowledge of upstream and/or downstream, as well as a general knowledge of the associated analytical, and media/buffer preparation techniques. Playing a key role in performing hands on evaluations and forming collaborations both internal to Amgen and with Vendors to advance upstream and downstream processing capabilities.
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We are seeking motivated individuals with experience and familiarity with enzymatic synthesis, standard chromatography techniques, TFF, DNA purification kits, and molecular biology techniques such as DNA manipulations including PCR, ligations, restriction digestions, and plasmid cloning.
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Effectively identify, analyze, and communicate downstream impacts of project changes; navigating project changes effectively by removing barriers. Sr IT Project manager. Effectively identify, analyze, and communicate downstream impacts of project changes; navigating project changes effectively by removing barriers.
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And with proteins expressed in mammalian cells with oversight of both upstream and downstream process development. Develop and optimize upstream and downstream processes to generate lead and Development Candidate TCR bispecific and to enable seamless technology transfer to contract manufacturing organizations.
ExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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The Product Manager will be responsible for upstream and downstream product management by assisting with project commercialization and sustaining activities linked with product line support, sales team support, market assessment, and product promotion (advertising, literature development, etc.
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Execute downstream contract administration, including Request for Information (RFI's), submittals, meeting minutes, change management, and claims mitigation. Assistant Project Manager / Construction Manager.
$42 - $51 an hourExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Experience of successfully integrating Informatica MDM to downstream systems via publishing layer. 5+ years of experience in installing, configuring, and upgrading Informatica MDM platforms like MDM Hub, PIM360, EDC, Axon, IDQ, BPM and Active VOS.
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You will work closely with stem cell scientists to coordinate experiments and sample analysis, using assays such as flow cytometry and cell sorting, single cell RNsequencing including captures and library generation, and downstream validation studies including qPCR and ddPCR. Your role will include diverse bench work spanning the functions of the Stem Cell Sciences program.
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downstream job in Lexington, MA
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