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The Quality Control Analyst I (RP/ISO) is responsible for conducting routine analysis of materials including: Raw Materials, in-process and finished formulations under general supervision and in accordance with standard operating procedures (SOPs.
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The Quality Control Analyst will work within the QC team, testing gene therapy products utilizing cell-based assays (Potency assay) in support of clinical and commercial lot release and stability activities.
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Responsible for Quality System records associated with analytical testing (change control, lab investigations, OOS, deviations, and CAPAs) Recruit, train, and develop a team of Quality Control professionals as needed.
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The Quality Control Documentation Specialist is responsible for performing the data review for the release of regulated and/or non-regulated materials including raw materials, in-process and finished products undergeneral supervision and in accordance with standard operating procedures (SOPs.
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These markets include aerospace and defense, factory automation, air and water quality environmental monitoring, electronics design and development, oceanographic research, deepwater oil and gas exploration and production, medical imaging and pharmaceutical research.
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SUMMARY OF JOB DUTIES: Efficiently operate CNC milling machines in a fast-paced manufacturing shop environment to meet the customer needs.
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As a CNC Lathe Machinist, you will play a crucial role in the production of precision components using Computer Numerical Control (CNC) lathe machines. The ideal candidate will have a careful understanding of CNC lathe operations, excellent attention to detail, and the ability to produce high-quality parts according to specifications.
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This Opportunity allows for a lot of growth and ability to work with QC Chemistry practices!
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As a Department representative on customer complaints, customer service and emergency service, employee must demonstrate a strong initiative and ability to effectively evaluate control room systems to assist in providing support for troubleshooting system , communicate ideas, technical information, and directions in a precise and courteous manner.
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Drive continued efficiency improvements through the effective use of metrics, 5S, and the PPI process Recommend and implement changes in manufacturing procedures to improve product quality and production efficiency.
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This involves the development of a control system architecture, selecting the components to be used, detailing schematic diagrams and system documentation, programming controllers (PLC, DCS, RTU), programming the process visualization (HMI/SCADA), developing databases for archiving/displaying historical system data and implementing/commissioning the control system at the client's facility.
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Proven experience with all phases of automation projects including conceptual, basis of design, implementation, testing, start-up and commissioning of Process Control System (PCS), SCADA, and DCS in the Life Science industry.
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JC Ehrlich is a member of the Rentokil family of companies, the global leader in Pest Control across more than 80 countries. Participate in employer-provided training on new methods, products, and services in the JC Ehrlich range of pest control solutions.
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Participate in project kick-off teams improving quality aspects of product introduction, and have a fundamental understanding of quality systems, SPC, and control plans. Support quality improvement efforts, Internal Auditing and Continuous Improvement initiatives.
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Take charge of programming controllers such as PLC, DCS, and RTU as well as in processing visualization (HMI/SCADA), building databases for storing/displaying historical system data, and commissioning the control system at the client's site is critical.
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quality control jobs Title: quality control representative Company: Planet Pharma in Andover, MA
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