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5-8 years of experience in a manufacturing quality manager, quality supervisor, or senior quality engineering role. DFT is looking for a Quality Manager to help lead the company through an exciting period of expansion of the Quality team and its structure.
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At Philips, we’re looking for a highly qualified Lab Analyst / Metrologist to join our quality team within the San Diego site ( Self-starter that can meet deadlines and maintain quality standards.
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Quality Engineer aims to ensure that the product or service an organization provides is fit for purpose and meets both external and internal requirements, including legal compliance and customer expectations.
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The candidate will have a strong technical background and a proven track record in Quality Control with methods related to biologics, small molecule, and AOC/ADC modalities. Support oversight of QC activities at CMOs, including SOW review, accountability for timelines and data quality, and communication of updates.
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Provide technical review for stability data from various assays across multiple product types, including mAb, oligonucleotide, and DS/DP AOC (Antibody oligonucleotide conjugate). Avidity Biosciences, Inc.'s mission is to profoundly improve people's lives by delivering a new class of RNA therapeutics - Antibody Oligonucleotide Conjugates (AOCs.
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Specific to CTC/PWC and MCC: training and perform quality assurance duties by reviewing medical documentation utilizing audit tools as outlined by County of San Diego Quality Management.
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Avidity is revolutionizing the field of RNA with its proprietary AOCs, which are designed to combine the specificity of monoclonal antibodies with the precision of oligonucleotide therapies to address targets and diseases previously unreachable with existing RNA therapies.
$98,000 - $120,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Manage the analytical testing of products (in-process, for information, and release) Review the testing schedule with the QC Supervisor Perform day to day analytical testing activities in GMP QC lab to support the on-time release and periodic testing of biological drug products using complex instrumentation and laboratory equipment’s per regulatory/quality policies.
$150,000 - $190,000 a yearFull-timeExpandUpdated 13 days ago - UpvoteDownvoteShare Job
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The QC Chemist I will be responsible for performing various analytical techniques and common standard lab practices in order to assess the quality of pharmaceutical products under cGMPs (as applicable) and limited supervision.
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Job Title Quality Lab Analyst Job Description. Must be able to work unsupervised and interact with other technicians, engineers, quality personnel and customers. If you’re an experienced professional who is passionate about quality and customer satisfaction, we’d love to hear from you.
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Performs NDT Inspection on shipboard welds and a variety of quality control tests/inspections on products, materials, components, parts, etc. Maintains appropriate documentation related to quality assurance tests and inspections.
$24 - $36 an hourFull-timeExpandUpdated 1 month ago - UpvoteDownvoteShare Job
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At VetPowered, the Quality Inspector will routinely perform first part, in-process, and final inspection of manufactured products using measuring equipment and sampling plans to ensure defects do not reach our customers.
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Quality Assurance NDT Inspector II. Prior experience in performing Quality Assurance support tasksassociated with mechanical and structural/piping/electrical repairand upgrades and installation of electronic systems on US Navy Ships.
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The Senior Manager of Drug Safety & Pharmacovigilance (PV) Quality, is a key role and is responsible for oversight of Drug Safety & PV quality, compliance, and alliance management activities, thus always promoting inspection readiness and maintaining a robust global compliance program within the Quality Assurance department.
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Minimum of 10 years relevant experience in GMP quality control in biologics. Reporting to the Head of Quality, you have the opportunity to significantly contribute to the oversight of high-tech CMC development laboratories in Forte’s outsourced network and help shape the future of biotech drug product development.
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quality job in San Diego, CA
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