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Join our team as a Food Safety/Quality Assurance Supervisor at our well-respected poultry processing plant in Monterey, TN! GMP Guru: Daily monitoring of plant GMPs (Good Manufacturing Practices) and other essential prerequisite programs to maintain top-notch quality.
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The Quality Assurance (QA) Manager is responsible for the planning, execution, and overall management of an FDA and GMP regulated Quality Unit which governs the site's manufacturing, packaging, labeling, testing, and holding activities of goods produced.
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Work closely with GxP Quality Assurance and functional areas responsible for the conduct of clinical research (e.g., Clinical Operations, Clinical Development, Biostatistics and Data Management, Pharmacovigilance, etc.
$155,000 - $190,000 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Experience in quality control or GMP within a cell therapy or biopharmaceutical manufacturing environment is preferred, including raw material release. with 5+ years of experience in quality control testing, analytical development, or GMP; OR a Master's degree in relevant scientific disciplines with 3+ years of experience.
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A minimum of 6 years’ experience in a GMP quality assurance (QA) role. The QA Engineer will be responsible to partner in the Quality oversight of IT and Automation (OT) systems through to operational readiness, as well as provide oversight of validation program execution for these systems.
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The QA Manager will develop, manage, and support Quality Assurance initiatives associated with the GMP oversight of the Quality Systems. Quality Assurance Manager, Validation (Gene Therapy Program.
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Quality, QA, assurance, GMP, manufacturing, distribution, packaging, CDMO, pharmaceutical, batch, release, systems, compliance, regulatory, specialist, investigations, CAPA, deviation, change, control, operations, senior, leader, supervisor, manager, coach, mentor.
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It is preferable that the candidate have experience working in an aseptic manufacturing facility, preferably in quality assurance, manufacturing compliance, clinical quality, or cell therapy.
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Complying with local legislation and ADM requirements for permitting, safety legislation, quality assurance, HACCP, GMP, Hazop as well as TPS policy. In this role, you will ensure high-quality work for projects greater than 25 million dollars with high financial impact and significance.
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Maintain an understanding of all products grown as well as the raw materials, packaging materials, and operations required in the production of these products including quality specifications and GMP / SQF standards.
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The Manager of Clinical Quality Assurance (CQA) is a key member of the CQA team and will perform day-to-day clinical quality operations and compliance activities to support the success of the clinical studies sponsored or supported by Corcept.
$144,800 - $170,300 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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The QA Specialist II, QA Production Support is responsible for performing incoming sampling of materials, support room /line clearances and provide QA input into production event resolution to assure that quality operations are in conformance to GMP requirements.
$30 - $35 an hourExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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The Quality Assurance Specialist will actively contribute to the implementation and maintenance of the Quality Systems Manual and conduct GMP compliance audits as directed.
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About the job Quality Assurance Technician. The role of this position is to assist the QA Manager in coordinating a facility-wide GMP/HACCP Food Safety Program, and to ensure these programs are adhered to, including facility compliance and achieving audit requirements.
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Technical Support – Provide technical support to Product Development and Operations in conducting process capabilities, Quality Assurance standards, quality procedures, food safety, and food security requirements.
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