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As the Source Document Specialist you will provide support to the Study Coordinator on a daily basis, ensure all activities are conducted according to company SOPs, and all applicable GCP and ICH regulations and guidelines.
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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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As a CGS Hmong Chinese Document Reviewer you will play a key role in supporting various aspects of the company's litigation portfolio including eDiscovery activities, workflow management, and litigation support.
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The R&D Technical Document Specialist performs work per the direction of the R&D International Project & Documentation Manager to coordinate the necessary research, documentation, support, and maintenance for global product registration from R&D product development.
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A Document Quality Control Specialist position (fully remote) is now available through Adecco Medical and Science. Working knowledge of bioanalytical assays (LCMS/MS, immunoassays, etc.
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In this role, you will be responsible for the quality control review of scientific documents within the Translational DMPK and Clinical Pharmacology group. Conduct Quality Control (QC) review of Bioanalytical data (LC-MS/MS, ELISA, qPCR, etc.
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This position reports to the Lead Document Specialist and/or the Land Manager. In some cases, assist the Document Specialist with inputting data. Oversees, mentors, and manages the day-to-day operation of the Document Specialist team.
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The candidate will be hands-on for processing and maintaining GxP quality management systems documents and records, implementation and management of an electronic document management system (EDMS/LMS/QMS), periodic review of SOPs and archival of quality records, and maintaining the GxP training program, including new hire onboarding.
$132,100 - $146,100 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Astrion has an exciting opportunity for a Document Control Specialist for the RWESS , supporting the Army. Document Control Specialist. The CM Specialist will properly document traceability of designs to requirements.
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The Quality Assurance Document Control Specialist role is an exempt position responsible for supporting the document management process within a cell therapy manufacturing facility to support both clinical and commercial requirements in a sterile GMP environment.
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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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Audubon Companies is currently seeking a Document Controller to be part of a project team headquartered in Texas City, TX. The Document Controller assists in maintaining project documentation files consisting of technical data, engineering and supplier drawings, technical specifications, purchase orders and other project-required documents.
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The Technical Document Specialist should be able to manage a document control system and suggest editorial and format improvements to current documentation standards. NYeC is seeking a Technical Document Specialist with to work with engineering and technical staff to prepare technical and end user documentation.
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The Document Control Lead will assist in overseeing document and record control operations, policies, and procedures the secure management and access of Cepheid controlled documents and records.
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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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Title: document specialist Company: Ineos Aromatics
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