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Perform material movements, transfer raw materials, chemicals into, out of, across the production areas. Candidates With the Following Backgrounds Have Had Success In Manufacturing At Client Combined With Scientific Degree, Manufacturing Experience Or Courses/Interests In Science: Food service Cooks (can follow recipes) Pharmacy techs Mechanical aptitude Robotics Computer skills (this is ever more important as our suites are more and more automated) EMTs Tech Support Anything in which they need to follow SOPs, Guidelines, industry regulations Sig Sauer employees Security guards Nurses/nurses aids.
Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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They support the production groups by ensuring the suites are appropriately stocked with raw materials and consumables, assemble and autoclave assemblies for use, clean soiled parts, perform daily/weekly maintenance on analytical equipment, and complete scheduled cleaning requirements that are not fulfilled by contracted cleaning staff.
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Work with the Legal Department on contract creation/management and with audit and other process partners to manage risk; Mitigate risk along the value chain, including raw materials/ingredients, packaging, inventory, and logistics.
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The candidate will champion continuous improvement efforts to establish an effective Quality Management System as well as oversee all Quality Control activities, including but not limited to biochemistry, microbiology, environmental monitoring, raw materials, stability, method validation, method transfer, instrument and software qualification, data integrity, sample management, and QC document management.
Full-timeExpandApply NowActive JobUpdated 24 days ago - UpvoteDownvoteShare Job
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10% Perform material movements, transfer raw materials, chemicals into, out of, across the production areas. The Manufacturing Associate is responsible for the manufacture of therapeutic proteins (API) under cGMP conditions.
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40% 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.
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10% Perform material movements, transfer raw materials, and chemicals into, out of, and across the production areas. 40% 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 by good manufacturing practice (GMPs) and good documentation procedures (GDPs), review documentation as appropriate.
$27 an hourExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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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.
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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. The Biotechnologist Associate is responsible for the manufacturing of therapeutic proteins (API) under cGMP conditions.
$27 an hourFull-timeExpandApply NowActive JobUpdated 25 days ago - UpvoteDownvoteShare Job
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0-3 years’ experience; some prior experience in a manufacturing setting preferred. Level I associates are expected to execute process recipes, follow written procedures (SOPs), monitor equipment and processes, perform basic laboratory tasks, including pH, conductivity, sampling, and conduct routine sanitization tasks to maintain facility and equipment.
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10% Perform basic laboratory tasks, such as monitor pH, conductivity, test product samples, etc. Proven Logic And Decision-making Abilities, Critical Thinking Skills. 10% Administrative tasks - attending shift exchange, meetings, sending/receiving emails, participating in projects, perform other duties as assigned.
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Good understanding of quality management principles (such as Good Manufacturing Principles), continuous improvement methodologies (such as Lean & Six Sigma), regulatory requirements (such as FDA, SQF, BRC, AIB), and industry best practices in relevant CPG sectors (frozen food manufacturing a plus.
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COMBINED WITH SCIENTIFIC DEGREE, MANUFACTURING EXPERIENCE OR COURSES/INTERESTS IN SCIENCE are also welcome. Must be willing to gown and work in a "clean room " environment. COMBINED WITH SCIENTIFIC DEGREE, MANUFACTURING EXPERIENCE OR COURSES/INTERESTS IN SCIENCE are also welcome.
$27 an hourExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Our client, SGS Consulting, is seeking the following. Level I associate are expected to execute process recipes, follow written procedures (SOPs), monitor equipment and processes, perform basic laboratory tasks, including pH, conductivity, sampling, and conduct routine sanitization tasks to maintain facility and equipment.
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