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Minimum of 4-6 years of experience in the medical device and/or pharmaceutical manufacturing environment. Ø Develops and maintains an effective cross-functional working relationship with plant and corporate Manufacturing, Engineering, Regulatory, and Quality Assurance personnel.
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Organize, write, and execute validation protocols associated with the manufacturing process. This includes, site standard operating procedures (SOPs), equipment documentation, capacity, setup, operation, disassembly, maintenance, cleaning, troubleshooting, monitoring, and programming of manufacturing equipment at the facility.
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Manufacturing Technician 1|MA. The position involves accurate and efficient manufacturing of sensor wafers and solutions. Printing application: use of screen printers with various precious metals to print sensor circuitry on to ceramic wafers.
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The Maintenance Mechanic is responsible for routine maintenance, repairs and troubleshooting on a wide range of manufacturing equipment, including but not limited to conveyors, presses, and other production equipment.
$63,000 - $83,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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As a Manufacturing Associate, you will play a pivotal role in our mission by contributing to the production process of cutting-edge mRNA therapeutics and vaccines. Execute manufacturing operations using disposable technologies, automation, and Manufacturing Execution Systems (MES) to produce mRNA.
$40 - $42.5 an hourTemporaryExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Oversee the hiring, training, development, and retention of manufacturing staff. Minimum of 5 years in a biotechnology manufacturing, quality, or development environment. Maintain a thorough knowledge of cGMPs and FDA guidelines to ensure all manufacturing processes meet regulatory standards.
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Strong working knowledge of Oracle Modules and data structure – Manufacturing, Quality, Inventory, and Manufacturing/Inventory data structures. The Business Analyst, Manufacturing & Quality will work closely with business stakeholders to understand current business processes and identify opportunities for improvement.
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Our client is in need of an experienced, licensed electrician who has experience in a manufacturing-type environment and who can work the overnight shift. Work onsite in the manufacturing plant overnight 3 – 4 days a week on 12 hour shifts.
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The Quality Assurance Sr. Specialist is based in Norwood, MA. This position is part of Moderna’s Quality Assurance team responsible for ensuring quality oversight of our mRNA platform in cGMP Manufacturing.
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Proven track record of solving manufacturing problems with cost effective solutions. Experience with 3-D solid modeling (e.g. SolidWorks, AutoCad. ProEngineer). Experience using SolidWorks desirable.
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Wafer preparation: electro-chemical chloridization, visual inspection, weighing of wafers and accurate record keeping. Duties include all steps from wafer printing through solution preparation. These sensors are assembled into j-body sensors and sensor modules.
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Lead and support troubleshooting activities to minimize process downtime or re-occurrence Identify key process indicators and collect data to drive manufacturing and yield improvements Responsibilities: Generation and execution of validation plans, validation protocols (IQ/OQ/PQ), and completion reports, with a major focus on sterilization and microbiology of medical devices.
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Role: Manufacturing Engineer II. manufacturing equipment, manufacturing processes, stability or aging, required. Lean/Six Sigma Green or Black Belt Certification is a plus. FDA, Notified Body (BSI) and Corporate, among others.
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Reporting to the Manufacturing Engineering Manager, the Manufacturing Engineer I - Manufacturing Production Quality Support position is a junior engineering position on the Manufacturing Engineering Team. This position supports the general manufacturing processes with a strong emphasis on production quality.
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Experience in validations such as: manufacturing equipment, manufacturing processes, stability or aging, required. Organize and write validation protocols associated with the manufacturing process.
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Title: manufacturing Company: Luttrell Staffing Group in Foxboro, MA
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