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Familiarity with MES infrastructure, HP ALM, Electronic Document Management Systems, Change Management Systems, and middleware WebMethods preferred. Familiarity with MES infrastructure, HP ALM, Electronic Document Management Systems, Change Management Systems, and middleware WebMethods preferred.
ExpandApply NowActive JobUpdated 13 days ago - UpvoteDownvoteShare Job
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Innova Solutions is immediately hiring for a QA Associate Specialist - Document Control. The Quality Assurance Document Control (QADC) Associate Specialist supports the cGMP Document Control operations for the Cell Therapy Above-site organization, including the document approvals, document change control process, periodic review and system reporting.
$28 - $32 an hourExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Test Equipment Console layout, ITA Design, Electrical/Mechanical Drafting, 3D Design and Modeling, Configuration Management Practices, Knowledge of Mil/ASME/ISO Standards, machining /manufacturing processes, materials/finishes, thermal calculations/management, Design Review preparation, estimation, and technical presentation package/document development.
Full-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Experience with MES infrastructure, ALM and Veeva document/change management systems and middleware WebMethods. With advanced technical document writing and time management skills, including ability to prioritize and manage expectations.
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Proficiency with Microsoft Office applications and document management systems (e.g. Datavision, SharePoint, Veeva Vault, SmartSheets) preferred. The Senior Manager, Scientific Communications & Publications, provides support to the Associate Director/Director for the development and execution of the global publications plan for the assigned therapeutic areas.
$116,000 - $161,333 a yearExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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If you are ready to challenge yourself, accelerate your career, and give new hope to patients, there’s no better place than here at BMS with our Cell Therapy team. With our bold ambition, backed by a best-in-the-industry team and long-term commitment, we are leading the way to unlock the full promise of Cell Therapy as we strive to put more patients on the path to a cure.
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The supervisor will coordinate, inspect, monitor, and document the performance of outside contractors performing Underground construction and maintenance on the client’s facilities. We are searching for an Underground Construction Supervisor / Manager to support our client in the New Jersey area.
ExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Establish and continuously optimize overall BSM processes across PrM. Support development of a strategy, including QCP, TS and CDx, and process to construct and execute plan document such as Pharmacokinetics (PK), Anti-Drug Antibody (ADA) and biomarker analysis plans, which aid in the construction of clinical development plans, clinical protocols, and in the submission of certain regulatory documents.
Full-timeExpandApply NowActive JobUpdated 13 days ago - UpvoteDownvoteShare Job
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The Quality Assurance Document Control (QADC) Associate Specialist supports the cGMP Document Control operations for the Client Cell Therapy Above-site organization, including the document approvals, document change control process, periodic review and system reporting.
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Generates SOPs and Work Practices within Celgene’s Document Management System and electronic work plan template and measurement data templates to establish the Use, Maintenance and Calibration plans for GMP equipment.
ExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Assist in the development and management of a facility document management program to track facility drawings, and project turnover packages. The purpose of the Facility and Reliability Engineer is to development and implement a Reliability Centered Maintenance (RCM) strategy to support client Summit West Cell Therapy Operations and to maintain a qualified and compliant facility operation status.
ExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Immediate need for a talented Manufacturing Systems Validation Specialist. Knowledge of cGMP, GxP, GAMP, and SDLC regulations, including 21CFR part 11 electronic records and electronic signatures, and good documentation practices with the ALCOA+ principles of data integrity, risk-based approaches to validation, Computer Software Assurance (CSA) principles.
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Position Summary:The Quality Assurance Document Control (QADC) Associate Specialist supports the cGMP Document Control operations for the Client's Cell Therapy Above-site organization, including the document approvals, document change control process, periodic review, and system reporting.
ExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Ensures consistency in data collection, derived data definition, analysis file structure, statistical analysis and result interpretation throughout the drug project; Leads the planning and analysis of integrated efficacy and safety data; Review the relevant sections of the electronic common technical document (eCTD.
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Conduct and document, per PATH Procedures, onsite QA/QC activities through use of: 1st Delivery Inspections, Unsolicited resumes include any resume or hiring document sent to WSP in the absence of a signed Service Agreement where WSP has expressly requested recruitment/staffing services specific to the position at hand.
Full-timeExpandApply NowActive JobUpdated 1 month ago
document job in Basking Ridge, NJ
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