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This position provides production support for analytical quality control testing of pharmaceutical raw materials and drug products. 3-6 years of demonstrated practical Quality Control experience in GMP regulated laboratory.
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Job Title - Analyst I, Quality Control Molecular Biology. Adaptable to perform in a fast-paced environment while still delivering high-quality results, this Analyst I - QC Molecular Biology will be required to have strong interpersonal skills and be able to work under minimal supervision.
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Participate in continuous improvement of laboratory safety and quality compliance. Executes routine procedures based on biochemistry methodologies, such as HPLC, UPLC, SoloVPE.Execute routine procedures based on bioassay methodologies, such as plate-based assays (ELISA, ddPCR, ribogreen), gel electrophoresis, western blot and cell based assays.
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Quality Control Analyst II , working in. Contribute to general operations and testing of the QC Molecular Biology laboratory. Review laboratory assay documentation for accuracy and timelines, evaluate preliminary results; aid in the development of test methods and participate with the team to meet group goals and perform routine laboratory duties.
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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.
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Sr. Quality Control Analyst/Group Leader. Like Pace, our customers are continually innovating and looking for quality candidates to support their important work. Execute routine procedures based on bioassay methodologies, such as plate-based assays (ELISA, ddPCR, ribogreen), gel electrophoresis, western blot and cell based assays.
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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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Author and review SOP changes; participate in change controls, CAPAs and other quality systems. Work independently and as a team player with quality and attention to detail. Promote and actively demonstrate the Lantheus values of Accountability, Quality, Efficiency, Customer Service, Collaboration, and Safety, as well as appropriate workplace behaviors and professionalism, including respect, flexibility, and a positive attitude toward work and others.
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Prepares reports for the AML Quality Control Manager and Senior Management. This role involves critical attention to detail and will also be accountable for generating periodic reports (metrics) that will be utilized by the AML Senior Management team to analyze quality trends and patterns.
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The Quality Control analyst will primarily be responsible for supporting early phase and commercial quality control activities. 3+years of experience in Quality Control in GMP environment.
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Our client, a leading Pharmaceutical company in Woburn, MA, is looking for a Quality Control Analyst- Microbiology to support the gene therapy program pipeline. Supports routine laboratory operations (equipment cleaning, laboratory cleaning, inventory control, logbook management.
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