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Keywords: Manufacturing Technician, Manufacturing process technician, process technician, batch record, cell culture, upstream, downstream, all stream, fill finish, central services, GMP, aseptic, harvest prep, harvest, vpro, sanitation, purification, QC, quality control, equipment, calibration, buffers, solutes, media prep, mixing chemicals, pH, LI, clinical LI, manufacturing.
$20 - $30 an hourFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Key responsibilities are performing GMP tasks associated with maintaining compliant Quality Control and Stability laboratories; providing sample management support for QC; and creating, reviewing and approving documentation.
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Responsible for supporting and maintaining the GMP clinical/commercial manufacturing and facility process equipment, Pilot Plant and QC laboratory equipment. The GMP Lead Maintenance Technician: A motivated self-starter with prominent levels of initiative.
$31 - $42 an hourFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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QA Scientist I: A Bachelor's degree in Medical Technology/Medical Laboratory Scientist, Biology, Chemistry or related field and a minimum of 1-3 years' experience with QC, GMP, GDP, and medical device company is required.
Full-timeExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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QC Analyst I requires a minimum of 2 years of hands-on lab experience with at least two analytical technology platforms, one of which must be HPLC; 2+ years GMP experience; and a Bachelor's degree in chemistry, physics, engineering, or related scientific discipline, with documented hands-on analytical experience in coursework.
ExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Work with Preconstruction, Estimating and Purchasing in development of Guaranteed Maximum Price (GMP) or initial project budget. Conduct thorough construction document reviews and examine all documents for constructability and Quality Assurance/Quality Control (QA/QC.
Full-timeExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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Reports to: Project Manager, Senior Project Manager or Project Executive. Lead the preconstruction effort as it relates to Project Engineering and the specific project needs. Ability to implement leading-edge technologies such as Building Information Models (BIM) and Lean to benefit the project.
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Position Description: The QC Expert Environmental Monitoring Technician will provide support for Parenteral Operations by performing environmental monitoring of the classified manufacturing areas and by performing utility sampling and analysis within the Parenteral Operations and QC Laboratory buildings.
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Support validation of analytical methods for new Biologics programs and their transfer to outsourced partners to meet GMP testing needs. The Senior Director Analytical Lifecycle Management is vital for the success of Commercial Biologics QC, providing strategic leadership and overseeing daily operations.
Full-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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This position requires a BS/BA in Virology, Cell Biology, Microbiology, Biochemistry, or related Science, with 5 years working in GMP virology lab or related experience. As a Supervisor of QC Virology, a typical day might include the following: Supervise the contract lab testing program for cell bank and unprocessed bulk (including the cGMP aspect.
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As the QC Analyst II you are expected to demonstrate expertise in both the theoretical and practical aspects of analytical chemistry. The QC Analyst II is an integral part of the Curia team, contributing to our success by conducting analysis of chemical intermediates and target compounds.
$57,000 - $71,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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The qualified candidate will act provide quality assurance support quality systems and compliance activities working cross-functionally with R&D, Product/Process Development, Manufacturing, Supply Chain, QC and QA.
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Catalent Biologics in Bloomington, Indiana is a state-of-the art, GMP manufacturing facility, providing one million sq/ft of drug substance manufacturing, drug product manufacturing, and related pharmaceutical services.
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Manage Quality Labs (micro and qc) as well as the document control function encompassing all quality systems. The Quality Manager (PC) will ensure that all Quality related functions are compliant with GMP regulations and consistent with company policies and procedures in addition to conducting audits that insure continuous control over materials, facilities and products throughout the production cycle.
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The Materials Control Associate III is accountable for GMP (Good Manufacturing Practices) materials control/warehousing operations for a Phase II/III GMP biopharma manufacturing facility.
Full-timeExpandApply NowActive JobUpdated 3 months ago
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