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0-1 Years related experience in a GMP /GLP lab. Associates in Science (AS) degree with 2-3 years industry experience OR Bachelor of Science (BS) degree with 0-1 years industry experience. The Reagent Formulations Associate Technician for Beckman Coulter Diagnostics is part of a formulation team responsible for the manufacturing of large volume reagents used in the medical diagnostics field.
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Adhere to SOP, SSOP, GMP, and HACCP guidelines when in the plant. The Yard Jockey will oversee the organization and product movement between warehouses. Prepare and stage production ingredients to be transferred.
$20 - $25 an hourFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Be able to schedule rooms, trainers, and resources and other required training (GMP, HR, EHS, etc. Knowledge of pharmaceutical manufacturing of biotechnology products, aseptic processing, and cell culture products.
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Science knowledge of basic lab techniques such as pH adjusting, and buffer prep preferred. Basic computer skills (MS office, Outlook, timekeeping, etc.) The Vision of production operation team is to ensure the advancement and optimization of the laboratory in order to move science and healthcare forward.
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Innova Solutions offers benefits( based on eligibility) that include the following: Medical & pharmacy coverage, Dental/vision insurance, 401(k), Health saving account (HSA) and Flexible spending account (FSA), Life Insurance, Pet Insurance, Short term and Long term Disability, Accident & Critical illness coverage, Pre-paid legal & ID theft protection, Sick time, and other types of paid leaves (as required by law), Employee Assistance Program (EAP.
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Follow all standard operation procedures and GMP and SOX guidelines for all designated functions. Assist with the daily cycle count program by verifying counts and reconciling discrepancies under the guidance of the Warehouse Lead worker.
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Position Summary Details The GMP Cleaner position provides the cleaning and upkeep of an assigned area. Must keep janitor’s closet neat and orderly and maintain equipment in good working order.
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Follow GMP requirements and Quality Systems & Regulatory Compliance Department policies. Support the Quality Manager and Regulatory Manager in maintaining compliance with applicable regulations and standards, such as FDA, SQF, and customer requirements.
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Assist with tracking and utilization of Learning Management System (LMS). Previous experience with viral vector manufacturing is a plus. Previous experience working with a Learning Management System.
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This individual will be required to accurately record information within documentation while maintaining strict adherence to FDA, GMP and ISO requirements. Monitor and maintain minimum Training Requirements in Master Control, Knowledge Connection, and Client.
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Assure compliance with FDA Quality System Regulations (QSR), Good Manufacturing Practices (GMP), and ISO regulatory requirements. Our buildings are modern, with employee accessible WiFi, dedicated break, quiet, and collaborative spaces, and an on-campus cafeteria.
$25 an hourExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Minimum of 6 months to 1 year related experience in a GMP/GLP lab. Minimum of 6 months to 1 year related experience in a GMP/GLP lab. Minimum Qualifications: Associates (AA) degree or basic chemistry laboratory classes.
$22 - $24 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Leads the team to ensure proper documentation and system updates are occurring with the warehouse manufacturing teams, including collecting & reviewing manufacturing batch tickets, providing guidance to team members as needed for compliance with operating procedures, and data entry support for the ERP system (NetSuite.
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It's the ripple effect that changes and improves everything for your family, your community, and the world. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability.
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Strong understanding of regulatory requirements and guidelines, including FDA regulations (21 CFR Part 11, Part 210, Part 211), EU GMP Annex 15, and ICH guidelines. Develop and execute equipment validation protocols and reports for various types of pharmaceutical manufacturing equipment, including but not limited to packaging machinery, incubation chambers, and storage units.
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