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Master Technician: All eight Series A1 thru A8 f. We Guarantee The Lowest PriceSince 1926, the Quirk family and VIP have been the place where New Englanders turn for the tires and professional auto service they need to keep their vehicles running at peak performance.
$28 - $40 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Master of Science degree in a relevant field such as mechanical engineering, materials science, or aerospace engineering or equivalent industry experience. Expertise with Finite Element Analysis packages, specifically ANSYS and/or Nastran.
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Experience evaluating and correcting data quality and completeness issues, drive consensus on attribute definitions, master data management and process re-engineering. We're looking for an experienced Senior Principal Software Engineer and thought leader to join our growing team focused on rationalizing data management and analytics in OCI's hardware and data center space.
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Design and develop data capturing tools: Electronic Data Capture (EDC) Systems (Eg: iMedidata Rave and IBM Clinical) eCOA, IRT; Manage electronic Trial Master File (eTMF) QC review eg: Veeva Vault; Lead the Audit and Inspection/Submission Readiness activities like documentation of QC and preparing Storyboards (Eg: FDA/EMA Submissions.
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Oversee the Trial Master File (TMF) and assist with periodic audit of the TMF. Oversee the Trial Master File (TMF) and assist with periodic audit of the TMF. Independently manage interactions with clinical monitors, data management, safety, regulatory, pharmaceutical science and QA team members, both internally and externally.
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Master in Landscape Architecture (MLA) and Registration as a Licensed Landscape Architect (or in process) preferred. Works on interdisciplinary projects as the Public Space & Urban Forestry (PSUF) representative, including neighborhood plans and large-scale urban design projects.
Full-timeExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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Maintenance of the Trial Master File and/or electronic Trial Master File (TMF and eTMF) according to ICH-GCP, and company SOPs. Collect, file, and track clinical trial associated study and regulatory documents for the Trial Master Files.
Full-timeExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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Bachelors or Master of science in Molecular Biology, Biochemistry, Microbiology or related field. Generation Bio is seeking an energetic and highly motivated molecular biologist with broad expertise in engineering and development of CRISPR/ Cas systems for therapeutic application.
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This includes coordinating master data management, data integration, security, end user assistance, IT collaboration, and ad hoc projects. Perform day-to-day application administration tasks, including month/quarter end support, forecasting and budget support, master data setup, maintenance of calculations and data integrations, and security/access design and management.
ExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Maintain quality and compliant documentation related to all aspects of site management including quality and ALCOA+ compliant monitoring visit reports, centralized monitoring reports, site contact reports, Trial Master File/Investigator Site File, etc.
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This candidate must be an experienced BI developer who is also able to manage requirements gathering and client interactions along with being proficient in common BI tools like QlikView, Qlik Sense, Tableau and Power BI. The candidate will be expected to work closely with Master Data Management, Data Warehouse, and Sales Operations teams to ensure overall project success.
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Strong proficiency with Microsoft Office tools required; experience with Document Control (e.g., Master Control) and ERP software (e.g., Syteline) strongly preferred. Deep subject matter expertise in multiple key technical aspects of commercial immunoassay development; including but not limited to protein chemistry, antibody screening, antibody: bead conjugation, assay diluent formulation; multiplexing; preanalytical sample processing; scale-up, assay optimization and troubleshooting; multivariate data analysis; analytical validation; clinical validation.
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E COAs, analytical validations/transfers, process validations, master & executed batch records, label proofs, specifications, executed batch record review and batch disposition of Drug Substance, Drug Product and Finished Products (oral solid dosage forms, parenteral, radio labeled materials.
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Review and approve the Validation Master Plan (VMP) for manufacturing process, aseptic process, and shipping validation, working cross-functionally with key stake holders and responsible functions to ensure the defined VMP activities are executed, maintained and all supporting documentation is complete and accurate.
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Responsible for supporting the management, oversight (CRO) and maintenance of the Trial Master File (TMF) In addition to its wholly owned clinical assets, Dragonfly has a deep pipeline of wholly owned preclinical candidates discovered using its proprietary platform, as well as productive collaborations with Merck, AbbVie, Gilead and Bristol Myers Squibb in a broad range of disease areas.
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master job in Lexington, MA
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