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Key Experience and Requirements: BS/MS/PhD degree in a Pharmaceutical Manufacturing/Engineering, Analytical Chemistry, Chemistry, or related Quality fields. Compliance Adherence: Ensure strict site adherence to regulatory requirements, including implementing SOP's, US FDA Good Laboratory Practices (GLP), and current Good Manufacturing Practices (cGMP) under preclinical to clinical grade testing.
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Reporting to the Accounting Manager, the Post Award and Grant Accounting Specialist is responsible for the grants management and preparation of all post-award financial reporting and accounting related to grants and sponsored programs.
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The Inventory Specialist is responsible for inventory management of medicated and non-medicated items. Use and maintain all inventory tracking systems, as well as utilize the point-of-sale record-keeping system/METRC to receive, track and adjust inventory.
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Overview Working in a fast-paced, high volume, dynamic environment, the Clinical Authorization Specialist will bring clinical expertise to the prior authorization and appeals processes and serve as a liaison and patient advocate between Dana Farber Cancer Institute and various health plans.
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MGH Gastroenterology has an opening for a Medication Prior Authorization Specialist. The Medication Prior Authorization Specialist is responsible for obtaining all medication prior authorizations.
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The Prior Authorization Specialist (PAS) is an essential role responsible for facilitating exceptional patient experience, by securing authorizations for all scheduled services related to medical and surgical admissions across entities.
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Selected Candidate can work out of Woburn or Andover, MA; Irvine, CA; or Ottawa, Canada As a skilled specialist in IC layout, candidate must have the ability to complete tasks in creative and effective ways, and work on assignments requiring considerable judgement and initiative.
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DescriptionThe Department of Youth Services (DYS) is seeking dynamic, positive and service-minded individuals to fill the role of Juvenile Justice Youth Development Specialist. The Juvenile Justice Youth Development Specialist is the front line residential staff serving youth committed to the care or custody of the Department.
$49,759.58 - $64,791.74 a yearFull-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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5-7 years of manufacturing engineering work, specific experience in metal fabrication and electro-mechanical assembly and test preferred. Manufacturing Engineer Greater BostonOur Client is seeking a highly motivated and forward-thinking Manufacturing Engineer to develop and evaluate new processes and improve current process capability, efficiency, and overall productivity in all areas of it’s manufacturing facility on new and existing electro-mechanical products.
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Optimize pilot plant and pre-clinical production performance to allow for fast, flexible processing of multiple manufacturing processes including plasmid DNA prep, mRNA transcription and purification, and LNP formulation, and oligonucleotide synthesis.
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The company focuses on producing cell culture products, instruments, and solutions that help customers streamline their discovery, development, and production processes, and by making custom cGMP bioprocess liquids that radically simplify customers' manufacturing workflows - regardless of batch size.
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The Prior Authorization Specialist (PAS) is an essential role responsible for facilitating exceptional patient experience, by securing authorizations for all scheduled services related to medical and surgical admissions across entities, including BWH OR procedures, BWFH OR procedures, FXB OR procedures and BWH/BWFH Endoscopy Suite procedures in accordance with standards established by the Department, Hospital, Medical Staff, and outside regulatory and accreditation agencies.
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The Compliance Senior Drug Safety Specialist will:Assist the DSPV team with document management activities, including maintaining electronic files and collaborating with cross-functional teams.
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Core Sterile Processing functions include receiving, sorting and decontamination of surgical/clinic items and instrumentation; inspection and packaging of single instruments and instrument kits; identification of appropriate sterilization method and cycle selection, appropriate documentation for all sterile processes; and accurate inventory assignment relating to the case cart build process.
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Candidate is required to have a broad functional knowledge of pharmaceutical sciences /the biopharmaceutical industry, with a clear understanding of drug development/commercial manufacturing of biopharmaceuticals as it relates to CGT products.
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