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Corgan is actively recruiting a Document Control Administrator to join our Aviation studio in San Antonio. Maintain current composite sets of drawings and manage document control.
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At dsm-firmenich, being a force for good is not optional.
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Provides training support to internal staff on the document control process. AmplifyBio is seeking to hire a Documents Control Specialist to join our growing team. 0-2 years in industry with GLP/GMP quality assurance/control experience.
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Corgan is actively recruiting a Document Control Administrator to join our Aviation studio at our Project Management Office near the Hollywood Burbank Airport. Track status of document comments and responses.
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A Document Quality Control Specialist position (fully remote) is now available through Adecco Medical and Science. In this role, you will be responsible for the quality control review of scientific documents within the Translational DMPK and Clinical Pharmacology group.
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Conduct Quality Control (QC) review of Bioanalytical data (LC-MS/MS, ELISA, qPCR, etc.) Working knowledge of bioanalytical assays (LCMS/MS, immunoassays, etc.) Conduct Quality Control (QC) review of Bioanalytical data (LC-MS/MS, ELISA, qPCR, etc.
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Assists Document Management Specialist II with loan corrections on exceptions received from the Custodian warehouse. The Document Management Specialist I will be responsible for all aspects of the preparation and shipment of collateral files and/or the process and shipment of final documents.
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Must possess an Associate/Diploma Degree in Nursing, or Health Information Technology (HIT) or an Advanced degree in nursing or medical field such as MD, DO, NP/APN or PA. In the absence of a college degree, must have 3 or more years' experience as an inpatient coder or clinical documentation specialist.
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A construction Document Control Specialist provides direct support to the Document Control Manager, keeps track of important project documents such as project plans, specifications, RFI’s and submittals, vendor contracts and contract modifications, and also creates reports for management.
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Overview Document Validation Specialist Carrollton, TX The Community Choice Financial® Family of Brands is looking for a Document Validation Specialist to join our team and become part of a dynamic corporate culture dedicated to supporting our stores and team members.
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Perform, lead, and coordinate control systems work with staff through project design development and construction document phases to complete documents on schedule. Travel to client facilities to participate in field activities to assess and document the current state of existing or installed control systems.
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The Document Control Specialist will be responsible for configuration management planning product configuration identification, configuration change management, configuration status, configuration verification and audit support to product teams in development of instrumentation for missile, aviation, and sensor systems.
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3+ years of experience in the pharmaceutical industry within a GMP Quality Control role; experience with cell therapy products is a plus. Minimum of 2 years experience in the pharmaceutical industry working in a GMP quality control laboratory.
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The Material Control Specialist I is an entry level position. Demonstrated computer skills and proficiency using office software and/or computerized inventory control system. The primary responsibility is to control and track materials from receipt through storage to issue.
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The Quality Assurance Document Control (QADC) Labeling Specialist supports the cGMP Document Control operations for the BMS Jump site, including the coordination, issuance, reconciliation, and management of production labels and records.
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Title: document control specialist Company: Puff Co
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