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The Technical Analyst II/III will perform responsibilities of a traditional lab analyst, peer reviewer, and new system implementation specialist. Perform Quality Control (QC) technical and scientific and compliance review of data and documentation generated by the Bioanalytical Operations group in support of regulated studies (e.g. GLP, GMP) and non-regulated.
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The QC Analyst will support the gene therapy program pipeline including but not limited to routine GMP microbiological testing of AAV vector such as bioburden and endotoxin. Adaptable to perform in a fast-paced environment while still delivering high-quality results, this Analyst I - QC Microbiology will be required to have strong interpersonal skills and be able to work under minimal supervision.
ExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Support QC deviations, investigations, root cause analysis, change control, and CAPA as needed. Revise SOPs, forms, protocols, data reports, and other controlled documents relating to QC microbiology testing and instrumentation.
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Vor Bio is seeking an experienced Quality Control Senior Analyst to be a part of the team responsible for the day-to-day operations assigned to the QC Microbiology group, including sampling of a cGMP manufacturing facility, testing samples in the QC Microbiology laboratory for batch release of advanced therapeutics including cellular and gene therapy products.
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Provide support to analytical development for QC analytical method validation and method transfer. Assist in QC sample management for internal and external testing samples. The individual will work in the QC laboratory located in Watertown, MA with potential to relocate to the Northbridge, MA QC laboratory when appropriate.
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Description Job Title: QC Analyst IILocation: Lexington, MAAbout the role:As a QC Analyst II, you will focus on the daily lab operations and execution of testing to support manufacturing operations /validation/or development studies.
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Key Responsibilities/Essential Functions Perform routine QC testing in accordance with SOPs and cGMP guidelines. Summary of RolePerform routine and advanced testing on incoming radioactive and non-radioactive materials, reference standards, solutions, finished product release and stability in QC Laboratory.
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In this role, the Molecular Biology Quality Control Analyst I will be responsible for supporting the gene therapy program pipeline, including but not limited to routine GMP testing of AAV vector analytical methods such as GC titer determination by ddPCR and qPCR, impurity testing, and other methods as needed.
ExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Our client is looking for a QC Analyst II that is heavily focused on biochemistry. Job Title: QC Analyst II. Our client is looking for a QC Analyst II that is heavily focused on biochemistry.
$40 - $50 an hourExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Skills:Inspection, GMP, Clean Room, Packaging, Quality Assurance Experience:Entry Level2 year(s) responsibilities: Perform routine QC testing and Visual Inspection in accordance with SOPs and cGMP guidelines.
$20 - $27 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Performs routine Quality Control microbiology testing including, but not limited to bioburden testing, plate reading, endotoxin testing, total organic carbon testing, conductivity testing, media growth promotion, and microbial identification testing.
$27 - $47ExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Contribute to general operations and testing of the QC Molecular Biology laboratory. Quality Control Analyst II , working in. Contribute to general operations and testing of the QC Molecular Biology laboratory.
ExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Provide support to the QC Analytical department for activities required to maintain CGMP status of QC Instrumentation hardware and software and to perform comparability studies for the implementation of analytical assays on new instrumentation.
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The Senior QC Analyst position interacts regularly with TScans Quality Assurance, Analytical Development, Process Development, Manufacturing, Facilities, as well as TScans external test laboratories, where applicable.
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We are looking for a Quality Control (QC) professional to join our team as a Senior Quality Control Analyst, supporting our internal GMP cell therapy manufacturing. This position supports the execution, transfer, qualification and validation of all QC analytical methods and activities necessary to support the release of cellular drug products at our Waltham cell therapy manufacturing facility.
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qc analyst jobs in Woburn, MA
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