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The successful candidate will have a strong understanding of PTC Creo Schematics and PTC Creo Parametric with Piping and Cabling Extension (PCX), Harness Manufacturing Extension (HMS) and Windchill PLM for electrical design and documentation.
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The Materials Control Associate I is accountable for GMP (Good Manufacturing Practices) materials control/warehousing operations for a Phase II/III GMP biopharma manufacturing facility.
$20 - $25 an hourExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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Deburr the required number of components correctly, and in a timely manner according to process documentation. Prior detailed manufacturing work utilizing a microscope, hand tools or other micro-manufacturing equipment preferred.
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The Manufacturing Associate I is responsible for the manufacture of therapeutic proteins (API) under current Good Manufacturing Practices (cGMP) conditions. Working experience in manufacturing; cGMP setting preferred, and/or some experience as an Associate Level I in bio-pharma industry.
Full-timeExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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The ME Support Drafter will be responsible for preparing detailed drawings and specifications of equipment, subcomponents, and individual parts for use in issuing jobs, parts books, service manuals, and other manufacturing documentation.
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The Manufacturing Associate I/II - Downstream is responsible for the execution of production activities for early and late-phase Cell Culture programs within a GMP environment. Position Responsibilities The Manufacturing Associate I/II - Downstream must follow the instructions depicted in SRs, EPRs, SOPs and forms.
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This includes tasks related to assembly, manufacturing, quality control, and overall support for the production team. As a Production Associate, you will be responsible for contributing to the efficient and smooth operation of the production process.
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Writes, maintains, and distributes quality assurance auditing and manufacturing documentation. Checks the implementation of the quality system to ensure the ongoing reliability of the manufacturing process.
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Job Title: Sample Management Associate / LIMS / Pharma Manufacturing. Responsible for supporting the sample management process for QC (pick up from manufacturing, maintaining chain of custody in LIMS, aliquoting/delivering samples to appropriate lab, etc.
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The Manufacturing Associate is responsible for the manufacturing of therapeutic proteins (API) under cGMP conditions. Set up, operate equipment, and monitor production processes, including clean-in-place (CIP) and steam-in-place (SIP) operations and report production in written and electronic documents in accordance with good manufacturing practice (GMPs) and good documentation procedures (GDPs), review documentation as appropriate.
Full-timeExpandApply NowActive JobUpdated 26 days ago - UpvoteDownvoteShare Job
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Title: Biotechnologist Associate. They are expected to attain a basic understanding of cGMP compliance while training under close supervision, demonstrating aseptic technique in handling of products and materials.
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Performs work under machine operator with fi Packaging Associate, Packaging, Associate, Manufacturing. Able to communicate quality issues, proper documentation, packaging requirements and machine malfunctions.
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Role : Regulatory Affairs Associate. Direct interaction with RA functions including Regulatory Operations, Submissions Execution, Regulatory Project Management, Strategic Area and other stakeholders such as Project managers, Manufacturing Plants, affiliates, R&D, Technical center & Product Developers.
ExpandApply NowActive JobUpdated 26 days ago - UpvoteDownvoteShare Job
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Basic Requirements: 3 years QA or QC experience in pharmaceutical manufacturing required Demonstrated knowledge and use of Compendial, US, EU, Japan and other regulations in the area of pharmaceutical manufacturing Demonstrated ability to communicate with cross-functional teams including good oral and written communication skills Ability to work independently as a Quality SME with minimal supervision.
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This position is part of the Dry Powder Media Manufacturing department located in Logan, UT and will be an onsite position. Knowledge and understanding of production process, work instructions, documentation configuration control, non-conforming and rework documentation requirements and operates within them to ensure that the product conforms to its specification Aware of and comply with Stop Order, Concessions, ESD, Calibration, Preventative Maintenance, Material Identification & Segregation, and Good Documentation Practices, as associated with this job type/position.
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