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In this role, you will perform and evaluate the analytical quality control testing studies to support assay characterization and qualification and Phase 1 manufacturing for cell therapy - collaborating with internal partners and external CMOs / CROs.
ExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Microbiology Quality Control Analyst. Maintain data integrity and ensure compliance with company SOPs and specifications, FDA, GLP, QSR and CGMP regulations. Experience in quality operations, biotechnology, pharmaceutical or similar GMP manufacturing environment.
ExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Quality control sample management experience in the pharmaceutical industry supporting cGMP areas preferred. The QC Sample Management Consultant position will be responsible for supporting the Quality Control team in the establishment of a robust GMP sample shipment process as well as internal sample tracking/reporting capabilities.
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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Reports to: Supervisor, Quality Control. Experience with cGMP and QC Sample Management in the pharmaceutical industry preferred. The QC Associate Operations position is responsible for executing sample management activities, which include control, receipt, and distribution of product, intermediates, raw materials samples, sample retention, reference samples, and stability samples at Fujifilm Diosynth Biotechnologies California (FDBC.
$30 - $34 an hourTemporaryExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Quality Control experience in the pharmaceutical industry supporting cGMP manufacturing including site qualification and utility validation preferred. Experience in cGMP for cell therapy testing is a plus.
ExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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And familiarity with GMP quality systems/processes such as change control, non-conformances, corrective and preventative actions, and. Ability to analyze problems, develop and propose engineering solutions in a scientific manner using data-driven techniques and analyses (e.g., Root Cause Analysis (RCA), Statistical Process Control (SPC), Six Sigma, Predictive Maintenance, etc.
ExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Participate in functions involving teams, which impact production, increase efficiency, generate cost savings, and improve quality. As a result, we must follow strict rules in our manufacturing facilities to ensure we are not endangering the quality of the product.
Full-timeExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Title: Microbiology Quality Control Analyst. May prepare monthly quality trend reports. At Takeda, our patients rely on us to deliver quality products. As Microbiology QC Analyst, you will work in the QC Microbiology Lab, being responsible for conducting biological or chemical and physical analyses on raw materials, in-process samples, final product samples and other samples collected from manufacturing areas.
ExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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Direct experience is highly desirable in environmental monitoring, personnel monitoring, sterile gowning, and aseptic process control in accordance with ICH, USP and FDA guidelines. Supports EM data management including data entry, data verification, data download, generation of crystal reports from LIMS to support data trending.
ExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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You will report to the Manager, Quality Control Microbiology. Job Title: Quality Control Analyst. Required to work an alternate work schedule (10-hour shift / 4 days a week.
ExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Quality Control/Assurance knowledge in a cGMP environment is required. Calipers, Bagging, Micrometer, GMP, sample processing, pH meter, viscometer, Microsoft Office, good laboratory practices, SOP, COA, GLP, Good Manufacturing Practices, NCMR, non conformance materials report, Inspection, Quality Control, Quality Assurance.
ExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Maintain an awareness of cGMP, Good Laboratory Practices (GLP), good housekeeping and safety in the laboratory. This position will assist Lab Technician and Document Control activities as needed.
TemporaryExpandApply NowActive JobUpdated 25 days ago - UpvoteDownvoteShare Job
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You will report to Microbiology QC Supervisor. Takeda is a patient-focused company that will inspire and empower you to grow through life-changing work. Certified as a Global Top Employer, Takeda offers stimulating careers, encourages innovation, and strives for excellence in everything we do.
Full-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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At Takeda, we are transforming patient care through the development of novel specialty pharmaceuticals and best in class patient support programs. May work and have exposure to hot, cold, wet environment/conditions, dust, gases, chemicals, liquid Nitrogen, and fumes.
Full-timeExpandApply NowActive JobUpdated 9 days ago
cgmp quality control jobs in Thousand Oaks, CA
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