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In this position the QC Inspector will be partnering with the Quality Control Supervisor assisting with the responsibility for the day to day operation of your assigned Quality Control group.
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Position Title: QC Analyst II - Biochemistry. Testing may include but not limited to samples from drug substance and drug product manufacturing stability and various protocol studies using approved test methods or test methods derived from QC technical protocols.
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The candidate must have strong detail-orientation, data management, data science and life science experience to perform and maintain external (client-facing) data transfers and communication while managing internal data organization and quality control (QC) needs at Invicro.
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Experience as a radiation oncology medical physicist, including clinical experience with linac calibrations and QC, treatment planning system QC and routine use, sealed isotope therapy and radiation safety, IMRT planning and delivery, computer systems quality control, and medical physics program documentation.
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Assists with the implementation of a comprehensive program for quality control of the radiation-producing equipment to assure their constant acceptable performance for patient safety and treatment efficiency.
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Experience associated with the management of the post-closing and pre-funding quality control process and ability to lead and train staff on QC/QA trends, issues, and processes. Implements and follows the QC/QA, mortgage compliance policy and guidelines established.
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Job title: QC Analyst II – Biochemistry. 20-30%: Support QC operations, including data review, data trending, maintenance of equipment and reagents, lab housekeeping, and compliance with quality systems (e.g., SOP revisions.
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Experience with control systems, PLC’s, SCADA, and Building Management Systems (BMS) systems preferred. Familiarity with BMS and process control system (PCS) operation, monitoring, and alarm response.
$51.3 an hourFull-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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This role will help establish the microbiology function at Elevatebio, including but not limited to; laboratory/clean room start-up and qualification, development of the environmental monitoring program and contamination and control strategies, and execution of routine QC microbiology assays.
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Title: QC Analyst II – Biochemistry. This position is expected to maintain operational and GMP readiness of the QC areas as well as maintain critical reagent inventory such as antibodies and cell banks at business appropriate quantities.
$57 an hourExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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Implementation and quality assurance of appropriate procedures for the planning and delivery of radiotherapy, including technical specifications/tolerances as well as the flow of procedures entailed in the process (including supervision and QC review of treatment plans and dose calculations.
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This role is responsible for the efficient and reliable operation of Takeda-owned building equipment and associated lab support systems for R&D labs, QC labs, and office buildings. Join Takeda as a Sr Facilities Mechanic – Lab Support where you will be responsible for routine performance of preventative maintenance and repair activities on lab support systems and equipment with the focus on analytical equipment and instrumentation.
$51.3 an hourFull-timeExpandApply NowActive JobUpdated 13 days ago - UpvoteDownvoteShare Job
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The QC Analyst II – Biochemistry will primarily focus on daily lab operations and execution of testing to support manufacturing operations, validation, or development studies. The role may also involve sampling activities, maintaining operational and GMP readiness of the QC areas, and managing critical reagent inventory such as antibodies and cell banks.
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The Senior Medical Writer will also format documents using StartingPoint, manage document development in Veeva and SharePoint, coordinate literature reviews and library oversight, perform quality control (QC) review and substantive editing, and other medical writing support as needed.
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This role supports the daily operations of the QC Raw Materials department, whose primary responsibility is the testing and release of raw materials for GMP use in manufacturing. Desired: Previous experience in a GMP QC role is preferred.
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