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Good working knowledge of plastics manufacturing processes including injection molding, extrusion, blow mold, thermoform and others. NOW HIRING a Manufacturing Tooling Engineer at our Winchester, KY location.
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Collaborate with vendors to bring alternative methods, materials, and equipment to manufacturing to improve molds and mold maintenance. Primary function is leading the mold development and mold maintenance using cross functional initiatives within IWT Engineering, Manufacturing, and outside vendors to construct high performance molds for all current and future product lines.
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Description: The Instrumentation and Electrical Technician is responsible for performing maintenance and repair activities in a cGMP manufacturing facility. Must be able to work in a high demand non-climate control manufacturing setting.
$24 - $45 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Minimum experience 3+ years of successful experience leading a plant maintenance department in an industrial manufacturing environment and/or 5+ years of supervisory manufacturing experience.
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Applies Lean Manufacturing principles and collects engineering data for process improvement. Bachelor's degree in Engineering or Engineering Technology, or 10 years of manufacturing engineering experience.
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Minimum experience 3+ years of successful experience leading a plant maintenance department in an industrial manufacturing environment. and/or 5+ years of supervisory manufacturing experience.
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The essential responsibilities associated with this position are oversight of the manufacturing operations (as dictated by cGMP, CFR, and Catalent SOP) through document review/approval, real time monitoring/approval of manufacturing activities and testing/approval of in-process and finished product samples.
$20 - $29.08 an hourExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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The Senior Cost Accountant is an integral member of both the Finance Department and the manufacturing site with responsibility for inventory accounting, monthly manufacturing close, analysis of variances, and the standard setting process.
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Maintain a full understanding of all Catalent SOPs and policies along with all cGMP and CFR guidance that are applicable to the manufacturing of solid oral dosage pharmaceutical products. The QA Associate is responsible for the Quality support functions associated with the manufacturing of solid oral dosage products for a given business unit.
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Works in a fast-paced environmental supporting the quality control department of a CMO for manufacturing of biologic bulk drug substance, sterile finished drug product, and fill/finish. This role is responsible for Environmental Monitoring sampling, analyzing, and aseptic monitoring and microbiological testing to support Phase I/II GMP manufacturing.
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Applies Lean Manufacturing philosophies such as but not limited to; value stream maps, Standardized work, JIT, PDCA, SMED, 5S, SPC, etc. Bachelor's degree in Engineering, Engineering Technology, or a minimum 10 years experience in manufacturing engineering role required, or a combination of education and experience.
$65,000 - $80,000 a yearExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Experience: •Prior experience working in a pharmaceutical, biotech or food manufacturing environment (regulated by GMP standards and requirements) is preferred; with specific experience in oral solid dosage manufacturing (fluid bed, granulation, blending, compression, pan coating, or encapsulation manufacturing processes.
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Six months to one year of previous factory / manufacturing experience preferred. Responsible for machining and/or assembling production parts, maintaining 100% quality with on-time delivery to customer.
$14.5 - $15 an hourExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Support QC in a CMO for manufacturing of biologic bulk drug substance, sterile finished drug product and fill/finish. Environmental Monitoring sampling, analyzing, and aseptic monitoring and microbiological testing to support Phase I/II GMP manufacturing.
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Supports the QC department of a CMO for manufacturing of biologic bulk drug substance, sterile finished drug product and fill/finish. Scope: Environmental Monitoring sampling, analyzing, and aseptic monitoring and microbiological testing to support Phase I/II GMP manufacturing.
Full-timeExpandApply NowActive JobUpdated 9 days ago
manufacturing job Title: vp manufacturing Company: Cybercoders in Winchester, KY
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