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Experience being responsible for quality control of all scientific data generated within the Nonclinical Pharmacology group. This position is responsible for the quality control of all nonGLP data generated in the Nonclinical Pharmacology group within GNAT unit of client.
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DPS Group is seeking a qualified Senior Quality Assurance Operations professional to perform batch disposition, batch record review, deviation, CAPA and change control support at the Boston, MA client site.
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CFS is seeking an experienced Quality Inspector to lead inspection and test activities for the SPARC project. Interface with Technicians on issues related to quality and help them in understanding and interpreting quality specifications and technical drawings.
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The Manager is a hands-on manager that can organize and lead a team of QC personnel, support and execute QC testing, and contribute significantly to overall Quality Control strategy The ideal candidate will have experience working in a GMP QC laboratory setting, experience with cell and gene therapy test methodologies, compendial safety testing and enjoy a fast-paced, collaborative, and vibrant startup culture.
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These markets include aerospace and defense, factory automation, air and water quality environmental monitoring, electronics design and development, oceanographic research, deepwater oil and gas exploration and production, medical imaging and pharmaceutical research.
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Performs quality control on medication orders and prepared medications and additional quality control activities as necessary (e.g., refrigerator temperature, compounding logs, hood cleaning, emergency cart, and controlled substance inventory, etc.
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Bioanalytical Data reviewer/ Quality Control - Contractor. This position is responsible for the quality control of all nonGLP data generated in the Nonclinical Pharmacology group.
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QA | Quality Assurance | Quality Control | cGMP | AAV Gene Therapy | CDMO | Biologics Manufacturing | Quality Operations | Quality Systems | FDA | CGT | Cell and Gene Therapy.
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As a CNC Lathe Machinist, you will play a crucial role in the production of precision components using Computer Numerical Control (CNC) lathe machines. The ideal candidate will have a careful understanding of CNC lathe operations, excellent attention to detail, and the ability to produce high-quality parts according to specifications.
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The incumbent will work cross-functionally with colleagues from Manufacturing, Manufacturing Science and Technology, Global Engineering, Validation, Process Engineering, EM/UM Quality Control, CMC Regulatory, and Quality Operations on the design of processes and technologies required to produce aseptic drug product to successfully commercialize an exciting and diverse portfolio of innovative cell and gene therapy pipeline programs.
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This position is responsible for the quality control of all nonGLP data generated in the Nonclinical Pharmacology group within GNAT unit of NovoNordisk. The role is focused on Data Quality Assurance/Quality Control.
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The role involves proficiency in NGS support protocols, including NGS library prep, DNA/RNA isolation, qPCR, sample quality control techniques, and various other molecular biology techniques.
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The QA Associate will support quality operations activities for the manufacture of cellular therapy products. BS/BA in a science/engineering field and a minimum of 3+ years working in Quality, with experience in cell therapy (or applicable) environment preferred.
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The Radiologic Technologist will also take part in Quality Improvement and Quality Control activities. The Radiologic Technologist is expected to produce high quality Radiographic images under the guidance of the Radiology Supervisor.
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HRV Conformance Verification Associates, Inc. supplies a highly integrated series of professional engineering and quality assurance/quality control services worldwide that span the steel, concrete, paint, mechanical, and construction industries.
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quality control jobs in Woburn, MA
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