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Artiva Biotherapeutics is seeking a skilled and motived Quality Control Associate for Environmental Monitoring (EM) who will be reporting to the Supervisor of Quality Control.
Full-timeExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Essential Duties and Responsibilities Manages processes and teams associated with control of nonconforming products, CAPAs, deviations, complaints management, complaint investigations, post-market surveillance, audits, quality system, document control, incoming inspections, product release, and other Quality Assurance related processes and teams.
$174,000 - $249,400 a yearFull-timeExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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Collaborate with cross-functional partners, such as Supply Chain, Manufacturing Sciences, Manufacturing Technical Support, Quality Assurance, Quality Control, Validation and Facilities to accomplish organizational objectives (e.g., meeting commercial demand, new process transfers, new manufacturing area commissioning and validation.
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The purpose of this position is to provide organizational management and leadership to the Quality Assurance Disposition and audit functions and ensure the cGMP compliance of all operational areas.
ExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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The Supervisor must collaborate with cross-functional partners, such as Supply Chain, Manufacturing Sciences, Manufacturing Technical Support, Quality Assurance, Quality Control, Validation and Facilities to accomplish organizational objectives (e.g., meeting commercial demand, new process transfers, new manufacturing area commissioning and validation.
ExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Artiva Biotherapeutics is seeking a skilled and motived Quality Control Senior Associate for Environmental Monitoring (EM) who will be reporting to the Supervisor of Quality Control.
$86,000 - $112,000 a yearFull-timeExpandApply NowActive JobUpdated 2 months ago - UpvoteDownvoteShare Job
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Poseida Therapeutics, Inc. is seeking an exceptional candidate to join our Quality team in San Diego, CA. The Specialist Quality Assurance candidate will have Manufacturing Quality Assurance (MQA) related responsibilities to ensure Poseida's starting materials, including Pipeline Products Support (PPS) materials and Clinical products meet cGMP requirements.
ExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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The incumbent works closely with Manufacturing Operations, Engineering, Facilities, Quality Control, Microbiology, Process Development, Supply Operations, Analytical R&D, Clinical and Regulatory Affairs.
ExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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As an Analytical Chemistry Scientist II Reagent Development Services – Analytical Method Development and Transfer Group, you will work in a dynamic, team-oriented environment, collaborating with internal and external partners to develop, validate and, transfer analytical methods to support formulation development, stability testing, and quality control testing of raw materials, intermediates, and final products in accordance with project timelines.
Full-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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A small cell therapy company based in San Diego, CA , emerging in the autoimmune sector, is looking to add a key decision-maker to its Quality Control team. Experience in Quality Control at a cell-therapy organization.
ExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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Effectively communicate and collaborate with internal Quality Assurance, Manufacturing, Quality Control, Procurement, PPS and Facilities teams. Review executed PPS and production batch records and associated testing data to ensure the records meet cGMP expectations.
ExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Quality Management Systems (including complaint management, CAPAs, deviations, change control, quality audit management, supplier quality management, etc.) In addition, our team also works on projects with clients to manage these Quality business processes for supply chain, manufacturing, commercial operations and R&D. This includes analyzing various cGMP and 21 CFR Part 11 regulations in the Regulatory Compliance area to determine impact on risk exposure.
Full-timeExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Deep understanding of cGMP regulations, quality systems, and regulatory requirements relevant to late-stage process development and manufacturing. Collaboration : Foster strong collaborations with internal stakeholders, including Research, Manufacturing, Quality Control, Quality Assurance, Regulatory Affairs, and Clinical Development teams, to facilitate cross-functional alignment and decision-making.
Full-timeExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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Knowledge of and adherence to all PCI, cGMP, and GCP policies, procedures, rules. Knowledge of and adherence to all PCI, cGMP, and GCP policies, procedures, and rules. The QC Supervisor coordinates the activities of the Inspectors in the Warehouse Receiving and Shipping area.
Full-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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7-10 years of experience in Quality assurance or Quality control in Biopharma/medical device industries. The quality manager's primary responsibility is to manage local COD Quality policies, procedures, and processes in compliance with cGMP standards and Azzur business processes.
ExpandApply NowActive JobUpdated 5 days ago
cgmp quality control jobs in San Diego, CA
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