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GMP Guru: Daily monitoring of plant GMPs (Good Manufacturing Practices) and other essential prerequisite programs to maintain top-notch quality. Join our team as a Food Safety/Quality Assurance Supervisor at our well-respected poultry processing plant in Monterey, TN.
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Quality Systems including, but not limited to, Customer Complaints, CAPA, Internal Audit, Validation, Change Control, ICH Stability Study, GMP Management Review, Supplier Management, and Mock Recall.
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Keywords: Manufacturing Technician, Manufacturing process technician, process technician, batch record, cell culture, upstream, downstream, all stream, fill finish, central services, GMP, aseptic, harvest prep, harvest, vpro, sanitation, purification, QC, quality control, equipment, calibration, buffers, solutes, media prep, mixing chemicals, pH, LI, clinical LI, manufacturing.
$20 - $30 an hourFull-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. Understanding of one or more of the following processes preferred: GxP systems Serialization Infrastructure (IT and/or OT related) Manufacturing Execution Systems (MES) Process Control Systems (PCS) and Building Management Systems (BMS) PI Historian.
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Demonstrated knowledge of efficient and safe manufacturing operations to include product and associate safety, product quality (success rates), throughput delivery and cost control (minimizing downtime and waste, optimizing yield.
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Cell Therapy or Biologics Manufacturing Facilities, and GMP/GLP Quality knowledge and experience, statistical analysis skills, ability to summarize scientific data from electronic databases, ability to write scientific material and prepare presentations of scientific content are strongly preferred.
$61,046 - $95,972 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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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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Key responsibilities are performing GMP tasks associated with maintaining compliant Quality Control and Stability laboratories; providing sample management support for QC; and creating, reviewing and approving documentation.
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The QA Document Control Supervisor role is an exempt level position with responsibilities for supporting the document management process within a cell therapy manufacturing facility to support both clinical and commercial requirements in a sterile GMP environment.
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Responsible for the planning, monitoring and executing of the defined capital project scope, ensuring cost, timing and quality objectives are met within a PSM and GMP environment. Support GMP production, comply with processes, procedures, instructions as needed to support all Arxada Quality systems.
$76,000 - $110,000 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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3-4 years of relevant experience in the pharmaceutical industry on writing laboratory investigations and experience with GMP documentation review, Quality Systems, and Health Authority Regulations.
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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. The QA Specialist will have oversight of and involvement in, GMP compliance for production of Clinical Trial Material (CTM), including work performed by Contract Manufacturing Organizations (CMOs.
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The service portfolio supports all stages of the drug development process and all functional areas of bio/pharmaceutical manufacturing, including method development, microbiology, process validation and quality control.
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Develops, evaluates, and improves manufacturing methods, utilizing knowledge of product design, materials and parts, fabrication processes, tooling and production equipment capabilities, assembly methods, and quality control standards.
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