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Routinely provide performance feedback and guidance to employees in addition to conducting formal evaluations and reviews QUALIFICATIONS BS or MS in analytical chemistry, biochemistry, or biotechnology or equivalence BS with 3+ years or MS (0+ years) of professional experience in the vaccine or pharmaceutical industry in the field of QC analytics or R&D. Preferred 2 years of experience in cGLP or cGMP lab.
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Part of the Global IT team, the IT Business Analyst / Application Engineer of GxP Systems is an on-site all-around IT Professional, responsible for the implementation and support of IT enterprise quality systems and laboratory computer systems.
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Role: QC METHOD Analyst. Routine release and stability testing experience and analysis in QC environment. Experience in troubleshooting assay performance. Routine release and stability testing experience and analysis in QC environment.
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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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Collaborates with Analytical Development team in the transfer of assays to QC. Maintains the QC/Microbiology labs and associated equipment daily. Reviews QC documentation, to ensure completeness, accuracy, consistency, and clarity.
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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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Reporting to the Director, QC Molecular Biology, the Analyst I - QC Molecular Biology will support 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.
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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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Responsible for routine/non-routine QC sampling, testing and data review according to Standard Operating Procedures (SOPs) Oversee sampling and storage of QC samples and maintain retain inventory ensuring accurate inventory and organization.
$45 - $48 an hourFull-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Performs automated and manual assays as detailed in departmental/plant SOP's and QC Monographs, including raw material, in-process and finished product. Through our Original Equipment Manufacturing (OEM) business line, we research, develop, and manufacture customized assays and biomaterials.
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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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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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DPS Group is seeking a full time QC Lab Testing Analyst for a client in Lexington, MA. DPS Group is seeking a full time QC Lab Testing Analyst for a client in Lexington, MA. DPS Group is a global EPCMV firm offering full-service solutions within the Life Sciences (pharmaceutical, biotechnology, and medical technology) and Advanced Technology (semiconductor, data center, and solar) industries.
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DPS is dedicated to delivering successful projects with a 'client-first' mentality and personal touch across a range of market sectors: Project and Program Management, Procurement, Design, Construction Management, Health and Safety Management, Commissioning, Qualification, and Start-up.
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qc analyst jobs in Waltham, MA
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