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We are industry leaders of prepress and flexographic plate manufacturing and digital print with over 50years of expertise. The VT Group is a dynamic suite of three POP design and manufacturing companies headquartered in Delaware County, Pennsylvania.
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Preferred Education and Experience: 5+ years of Industrial Automation Controls Engineering experienceBS in Electrical, Mechanical, Mechatronics, Controls, or Manufacturing Engineering. Essential Functions: Possess top level technical knowledge of PLC/PC/HMI/robotics (Mitsubishi, Festo, Balluff, Standard Bots)Design, configure and troubleshoot electrical and pneumatic solutions.
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Demonstrated working knowledge of design controls, analytical, clinical, and manufacturing process validation requirements for IVDs, GCP, GLP, and GMP requirements; working knowledge of requirements for US and global regulatory submissions related to IVDs for use in clinical trials and for commercialization of companion diagnostics.
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Minimum of 2 years of experience in biopharmaceutical based GMP manufacturing operations. Proactive, results oriented, self-starter with demonstrated strong leadership skills and experience in a complex manufacturing environment.
$85,000 a yearFull-timeExpandApply NowActive JobUpdated 13 days ago - UpvoteDownvoteShare Job
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We are looking for a person with a controls engineering (or technical, industrial automation background) to become our Mitsubishi Automation Product Specialist. Competencies: Excellent written and verbal communication skillsExcellent organizational and time management skillsExperience with Industrial Automation Hardware and PneumaticsExperience designing Pneumatic and Electrical Automation SolutionsSelf-starter that will take direction and execute a plan with little supervision.
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Our custom research and development approach is designed to integrate into services, including platform bridging, GLP toxicology material, and GMP manufacturing. Through a comprehensive production workflow that utilizes VintaBio's proprietary cell lines and transfection reagents, we expedite the path to the clinic, offer more reliable manufacturing, and improve economics.
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The Lead Cell Manufacturing Technician's responsibilities will be:Develop a Subject Matter Expert-level understanding of GMP cell therapy manufacturing processes. Proven working experience in biopharmaceutical based GMP manufacturing operations, including experience in cell culture and associated downstream processing.
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Primary ResponsibilitiesAbility to develop a product from concept through productionCreation of 3D models and assembliesProduct Documentation; including Bills of Materials, installation sheets, and specification data sheetKnowledge of sheet-metal, metal and plastic extrusion, die-cast, thermoform and plastic injectionWork with Manufacturing throughout development process.
$40 - $50 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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JOB PUPOSESet ups, adjusts, maintains and operates various pieces of equipment, i.e. automatic glass washers, depyrogenation tunnels, cappers, tray loaders and automatic bag openers while complying with GMP regulations as well as internal SOPs. Utility Operator II also provides support to Group Leader, Manufacturing as may be required and serves in a Group Leader-Manufacturing capacity when required.
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Our comprehensive capabilities and teams include preclinical research, clinical development, translational sciences, autologous and allogeneic manufacturing, and in-house commercial and corporate operations.
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Bachelor of Science degree from an accredited course of study in engineering, engineering technology (includes manufacturing engineering technology), chemistry, physics, mathematics, data science, or computer science.
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For 100+ years, our client has providing full service steel fabrication and installation for industrial, manufacturing, institutional and food processing industries. Examples: Steel manufacturing tanks, Undercarriage, support structures, steps, catwalks & gangways & railings (lots of these systems), etc.
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Working knowledge and technical understanding of cement manufacturing process and its equipment, process control systems, and lab systems. Role operates in a manufacturing environment with moving mechanical equipment, inclement weather, heat, humidity, elevated noise levels, and dusty conditions.
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The Quality Control Analyst I- Microbiology will support quality control testing operations at Iovance’s Cell Therapy Center (iCTC) and/or iPBMC manufacturing site (IOVA). This position will work in both an office and a manufacturing setting.
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The candidate will work within the Bioprocess Clinical Manufacturing & Technology department's Automation Team to implement Dynamic Equipment Connectivity Dashboard on Ignition SCADA application.
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manufacturing job Company: Liberty Personnel Services in Philadelphia, PA
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