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Implement and adhere to quality management systems, including Good Laboratory Practices (GLP) and ISO standards. Main duties include: Design and execute experiments using a wide range of analytical techniques, including chromatography (HPLC, GC), spectroscopy (UV-Vis, FTIR, NMR), mass spectrometry, and thermal analysis.
$75,000 - $85,000 a yearExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Ensures compliance with applicable Inova standard operating procedures (SOPs), ISO, FDA and other Quality System regulations, as well as applicable Environmental Health & Safety, Human Resources and all other regulatory and administrative policies.
$20 - $27 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Separate internal QA team], Design Review Quality Assurance [independent peer review contracts], Design QMS Development/Maintenance (structure, leadership (LMAP), MQP, QMP) such as compliance audits, Project Performance KPIs and other performance requirements, and Continuous Improvement (IPA, LL, NCR, incremental change over time.
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Provide support for general QMS activities including audits, vendor management, and document control. Execute the QMS training program including keeping a current training matrix, conducting SOP training, and documenting external and GXP knowledge training.
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Demonstrate commitment to the development, implementation and effectiveness of Alere Quality Management System per ISO, FDA, and other regulatory agencies. This role will be responsible for delivering the implemented solutions and leading the development of QMS deliverables.
Full-timeExpandApply NowActive JobUpdated 13 days ago - UpvoteDownvoteShare Job
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4 years of experience in US deregulated electricity markets including ERCOT, PJM, ISO-NE, NYISO, MISO, and. 4 years of experience in US deregulated electricity markets including ERCOT, PJM, ISO-NE, NYISO, MISO, and.
Full-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Ensures that toxicology studies and programs are conducted in accordance with the appropriate guidelines and regulatory test standards (FDA, WHO, GLP, and ISO). Advises and directs the preparation of Safety Pharmacology and Toxicology sections of regulatory documents (IND, CTA, NDA, briefing books, Investigator Brochures, etc.
$217,300 - $314,725 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Experience leading QMS implementation, maintenance, and improvement initiatives, including CAPA, change control, and risk management processes. Champion, maintain, and support continuous improvement to the combination product QMS, monitor and identify areas for improvement and ensure remediation.
ExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Generally knowledgeable and/or supports Lean Management (COS) and regulatory (e.g. ISO, FAA, ITAR, etc.) Carlisle, Providien Thermoforming, is a clean facility housing different kinds of machinery, equipment, processes and chemicals which produce potential hazards in the work environment such as: ergonomic, chemical, machine point of operation, and powered industrial vehicle traffic.
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Review production and service orders and implement production and service schedulesAnalyze and diagnose equipment problems and take corrective measures to minimize downtime and interruption of schedulesEnsure the facility is meeting all regulatory and non-regulatory compliance obligations including, but not limited to, occupancy permit/business license, fleet compliance and ISO quality systems and certificationsDrive growth and change in a fast-moving and high-energy environment.
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Drive continuous improvement to BDs QMS processes and procedures. Ensure product development and validation programs meet requirements of FDA, ISO, local and international regulations when applicable.
ExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Drive a culture of quality throughout the organization by promoting adherence to QMS procedures and fostering continuous improvement initiatives. · Lead the development, implementation, and maintenance of comprehensive Quality Management Systems (QMS) to ensure compliance with relevant standards, regulations, and industry best practices.
$250,000 - $350,000 a yearExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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Create SOPs, WIs and Forms that efficiently and effectively control processes and meet our ISO and regulatory requirements, and ensures all personnel are trained and complaint to the appropriate new and existing procedures in a timely manner.
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Oversee all QMS activities, including but not limited to training, customer feedback management, deviations, corrective actions, supplier quality, and change control. This position requires a dynamic individual who will serve as the Subject Matter Expert in Quality, providing regular updates to Executive Management on the status of the Quality Management System (QMS.
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Relevant certifications for ISO or ASQ are desirable. The Director of Quality manages the development, implementation, and maintenance of Biosero’s Quality Management System (QMS) and processes.
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iso qms jobs in Poway, CA
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