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Supports the maintenance and continuous improvement of the overall quality system or a specific procedure, including management review, CAPA management, internal quality audits, quality self-assessments, change control, document control, and standard operating procedures/work instructions.
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Bid document review, pre-bid meetings, client interface, quantity takeoff, material, equipment and subcontractor pricing, spreadsheet input and proposal preparation. Specific expertise with Plumbing systems serving hotels, student housing, laboratories, power plants, Cogeneration facilities, manufacturing facilities, clean rooms, cGMP facilities and process systems for Pharmaceutical and microelectronics facilities is desired.
$86,000 a yearExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Manages document review and approval to meet project timelines and provides status reports to management. A working knowledge of safety, quality systems, and current Good Manufacturing Practices is required.
Full-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Tri-Pac, Inc. a contract development and manufacturing company (CDMO) specializing in liquid and aerosol filling for personal care and pharmaceutical marketers, is seeking an experienced QA Document Control Specialist for immediate addition to our fast growing team.
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The candidate in this role will be trained on day-to-day shop document control processes using the tools of an industrial ERP system (Globalshop) and will be responsible for ensuring certs from material/finishing POs are mapped properly throughout multi-stage subcomponent manufacturing processes.
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The Quality Control Inspector will review device history records & document their work on the DHR. Inspect components utilizing inspection equipment. Perform quarantine and receiving inspection of incoming raw materials, controlled manufacturing materials, machined components, labeling instrumentation, and packaging materials.
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Efficiently manage the review and release of these documents within the Picocyl document control system. The successful candidate in this position will:Manage manufacturing engineering projects:Handle all aspects of projects to onboard new product lines and new manufacturing equipment, and to optimize existing production processes.
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Work with Quality on Document Control and Contract Review to ensure proper setup and utilization of equipment and processes. · Lean Manufacturing/Six Sigma Knowledge. · Minimum 3 years’ manufacturing experience; experience with composite prepreg is an asset but not a requirement· Bachelor’s degree in mechanical or chemical Engineering· Web handling - tensioning, steering/guiding, unwinding, winding would be an asset.
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Document and communicate review metrics for assigned CMO/CTL (e.g., data integrity issues observed, untimely data package deliveries). This position reports to the Associate Director Quality Product Testing and will oversee compliance of GMP activities for assigned Contract Testing Laboratories (CTL)/Contract Manufacturing Organizations (CMO) as it relates to QC testing of ImmunoGen products.
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Ensure that document control procedures are utilized to approve, review, and update all changes to critical documents within the scope of the QMS. Formulates quality control objectives for the facility, such as defect reduction and operator certification for specified quality tasks and coordinates the objectives with production management and manufacturing procedures to maximize product reliability and minimize costs associated with rework, scrap, and escapements.
ExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Accountable for the completion of Monthly and annual trending, EMPQs and related document updates, deviations and investigations related to environmental monitoring process, and the review and approval of completed production and laboratory documentation (for example: log books) for quality, completeness, and cGMP (Good Manufacturing Practices) compliance.
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Contribute to CMO Manufacturing oversight via document review, person in plant responsibilities, and troubleshooting when necessary. Experience working with CMOs highly desired; ability to effectively transfer processes to CMO, and to oversee development and manufacturing activities performed at CMO; ability to travel to CMO (some international travel required) to perform person-in-plant oversight activities.
$129,000 - $146,000 a yearFull-timeExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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Hands-on experience with enterprise systems such as ERP systems, document management systems, project management systems, laboratory information management systems, learning management systems, electronic batch records, or manufacturing execution systems is ideal.
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Experience with MES infrastructure, ALM and Veeva document/change management systems and middleware WebMethods. Provide CSV & validation Production and Project support to S12 MES Next Gen. Complete all tasks required per the Change Management Process for S12 MES Next Gen SOP and in compliance with CSV and related SOPs. Review the summary reports from testing/validation to ensure all issues are resolved and approved.
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The Quality Assurance Associate will be responsible for quality problem resolution at our new King of Prussia, PA manufacturing plant and will focus on continuous improvement in quality, batch review, process control and new product production.
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document review manufacturing jobs
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