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In this role you have the opportunity to At Philips, we’re looking for a highly qualified Lab Analyst / Metrologist to join our quality team within the San Diego site ( note that this role requires the individual to be on site 5 days a week.
Full-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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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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DESCRIPTIONUnder the supervision of the Principal Investigator (PI), the employee will assist in research on uncovering principles of cellular protein quality control by carrying out various biochemistry, cell biology and molecular biological procedures in mammalian cells and Zebrafish.
$21.39 - $23.06 an hourFull-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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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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Catalent Pharma in San Diego, CA is hiring a Senior Manager of Quality Assurance (QA) at our Clinical Supplies facility. The primary responsibilities of the Senior QA Manager include activities related to GMP (Good Manufacturing Practices) and regulatory oversight, quality support to operations and coordination of audit activities affiliated with assigned projects.
$152,000 - $163,750 a yearFull-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Proactively provide Good Pharmacovigilance Practice (GVP) support for clinical and commercial activities to protect patient safety and well-being, maintain data integrity, and support implementation of Quality Systems.
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Support oversight of QC activities at CMOs, including SOW review, accountability for timelines and data quality, and communication of updates. Provide technical review for stability data from various assays across multiple product types, including mAb, oligonucleotide, and DS/DP AOC (Antibody oligonucleotide conjugate.
$98,000 - $120,000 a yearFull-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Laboratory duties will include detection of modifications by PCR/qPCR, analyses of fish growth and gene expression, and generation and handling of next generation sequencing data. Skills with data analysis using tools such as R, Python, Bash, Linux/Ubuntu.
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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. This position will oversee stability data generated at CMOs/CROs relating to the GMP testing of Avidity's products, including drug substance intermediates, drug substances, and drug products.
ExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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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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DataAnnotation is committed to creating quality AI. Join our team to help train AI chatbots while gaining the flexibility of remote work and choosing your own schedule. Note: Data Annotation payment is made via PayPal. We will never ask for any money from you.
$20 - $25 an hourExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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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 selected candidate will be responsible for all aspects of Quality Control oversight, including external (CDMO) release and in-process assays, raw data review, method qualification and validation, stability, trending and GMP investigations for any analytical deviation, OOT or OOS. The ideal candidate must have experience with cell therapy analytical techniques, including flow cytometry, PCR (qPCR, QF-PCR, ddPCR, and/or dPCR), ELISA, safety-based assays (sterility, mycoplasma, endotoxin, etc.
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Experienced with analysis of data extraction and analysis for the Aegis Weapons Control System. Interface with equipment In-Service Engineering Agencies (ISEA), Combat System Engineering Agent (CSEA) and Software Support Activities (SSA) to research and resolve WCS and FCS system anomalies.
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Reporting directly to the Disease Team Project Manager, the Data Coordinator is responsible for coordinating and managing the ongoing collection, quality assurance, and analysis of data for low to moderately complex oncology clinical trials.
Full-timeExpandApply NowActive JobUpdated 15 days ago
data quality jobs Title: quality manager in San Diego, CA
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