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QA Scientist I: A Bachelor's degree in Medical Technology/Medical Laboratory Scientist, Biology, Chemistry or related field and a minimum of 1-3 years' experience with QC, GMP, GDP, and medical device company is required.
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Ensures city, county, state, and federal regulations relating to the QA/QC laboratory are met at all times. Participates in the safety program for the QA/QC laboratory.
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Develop project proposals, project plans, manpower plans, budgets, schedules, negotiate fees, change orders, contracts, and overall QA/QC management. RMF Engineering provides planning, design, engineering, commissioning, and facility assessment services globally to clients in the healthcare, higher education, laboratory/research, and government sectors.
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Serve as a backup Quality Control (QC) analyst for routine testing procedures in the CQC laboratory. This position will serve as the primary point of contact for Plant QA/QC laboratories, addressing requests for instrumentation support, special sample analyses, and troubleshooting issues.
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This position will be responsible for testing and assisting Microbiology staff with routine water quality microbial testing, adhering to departments daily QA/QC requirements, as well as supporting other laboratory needs that may arise.
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May perform QC and QA as assigned by the supervisor after competency is demonstrated. A minimum of a two-year diploma or equivalent in any biological science or chemical science from an accredited/approved educational institution and successful completion of the Medical Laboratory Technology training program which includes Blood Banking (Immunohematology), Chemistry, Hematology, and Microbiology; OR A minimum of a two-year diploma in Medical Laboratory Technology which includes Blood Banking (Immunohematology), Chemistry, Hematology, and Microbiology.
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The QC Reviewer is responsible for compliance with Standard Operating Procedures (SOP) and Good Laboratory Practice (GLP) requirements at Pharma Medica Research Inc (PMRI), as well as raw date verifications, preparation of analytical reports and maintenance of laboratory log sheets/books.
ExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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We are hiring a QA/QC Technician to join our growing team! Able to lead team meetings to present, discuss, or train others on QA/QC topics and issues. Validates laboratory equipment accuracy weekly using calibration standards (weights, gage blocks, etc.
ExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Communicate directly with maintenance department and QA/QC laboratory on policies and procedures. 5 years' experience in the operation of a dry-mill ethanol plant. ethanol, grain, process engineer, process, process optimization, production manager, production.
$100,000 - $140,000 a yearFull-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Responsible for all phases of project management for the implementation of geotechnical studies, engineering analyses & recommendations, and construction consultation, including but not limited to client interaction, proposal preparation, budget and scheduling, billing and technical oversight, report preparation, internal QA/QC, and project scope delivery and execution.
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Currently hiring a long term opening in a Food Science Laboratory working with different sauces. Packaging/QA checking labels and code dates, checking bottles for cracks, leaks and weighing them and doing all documentation.
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Assist in maintaining a clean and organized lab in compliance with QA/QC initiatives and accreditation requirements, including calibration of laboratory equipment and maintenance of calibration schedule and records.
ExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Example: PI Team participation, QA/QC data collection, payroll, Lean Team member and or conducts mandatory in-services. Acts as a resource and is a liaison between phlebotomy staff and Laboratory /Point of Care Team. Cross trained in defined core job functions and patient care departments.
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Basic Requirements: 3 years QA or QC experience in pharmaceutical manufacturing required Demonstrated knowledge and use of Compendial, US, EU, Japan and other regulations in the area of pharmaceutical manufacturing Demonstrated ability to communicate with cross-functional teams including good oral and written communication skills Ability to work independently as a Quality SME with minimal supervision.
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Utilizes laboratory computer information system to include all work aides and shortcuts within the system. Complies with requirements of accreditation and regulatory agencies by attending mandatory in-services and continuing laboratory education and participating in continuous quality improvement.
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