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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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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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The minimum salary for this Sustainability Analyst position is $50,000 annually and the maximum salary for this position is $65,000 annually. Create and QA/QC project documents for compliance with building certification requirements, including, but not limited to, LEED, WELL Fitwel & BREEAM.
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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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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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A biopharmaceutical company is seeking a highly motivated QC Analyst for their office location in the Woburn, MA area. Support QC deviations, investigations, root cause analysis, change control, and CAPA as needed.
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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.
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Revise SOPs, forms, protocols, data reports, and other controlled documents relating to QC microbiology testing and instrumentation. 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.
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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.
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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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Periodic review of QC lab Systems (Document review. Have you done any work in MFG GXP environment or a QC GXP environment and if so what. Mettler Toledo Lab)(, Thermo WebAdmin for TruScan RM Analyzer, and vartous Laboratory desktop applications used in GxP environment.
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Reporting to the QC Manager, Internal Operations, this position will be responsible in conducting activities associated with product release testing at Editas Medicine QC laboratories. Partners with peers in manufacturing, engineering, validation, logistics, Corporate QA, and Corporate QC to ensure adherence the QMS and effective issue resolution.
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Role: QC Analyst. Manager is looking for folks well versed in QC, protocol writing, method development/ validation, GMP with tech transfer, API. Wet chemistry, UPLC/HPLC, etc. These aren’t your average QC roles, and consultants NEED METHOD DEVELOPMENT/ METHOD VALIDATION/ TMV on the resume for tech transfer.
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qc analyst jobs in Cambridge, MA
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