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We are seeking a quality control professional from the chemicals, pharmaceutical, or biotech industries to assist in the analysis and verification of a range of flow battery electrolyte samples.
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The Quality Control Analyst I (RP/ISO) is responsible for conducting routine analysis of materials including: Raw Materials, in-process and finished formulations under general supervision and in accordance with standard operating procedures (SOPs.
Full-timeExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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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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This individual will support quality control activities related to custom raw material manufacture for RNA and AAV gene therapy products conducted both internally and at various contract manufacturing organization (CMO) sites.
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The Quality Control Laboratory Support Technician (RP/ISO) is responsible for inventory management, glassware cleaning, and basic equipment verifications within the Quality Control department.
Full-timeExpandApply NowActive JobUpdated 25 days ago - UpvoteDownvoteShare Job
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Cambridge Isotope Laboratories, Inc. (CIL) is searching for a Quality Control Analyst I, that will be primarily focused on wet chemistry, based onsite in our Andover, MA facility. CIL's growing customer base spans academia, pharmaceutical, medical diagnostic and semiconductor industries enabling collaborations with Nobel laureates, industry-leading scientists, and chemists.
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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 position requires knowledge of quality systems, statistical tools, lean six sigma methodologies, process capability, and understanding of control plans and process flow. This position works closely with the Technology, Product Management, Reliability/Test Engineering, Consumer Care, Service, 3rd party logistics and other Quality teams on multiple activities in support of on-going product quality/ reliability improvement efforts.
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Two to four years of experience building, developing, and managing GMP Quality Control testing teams is required. Develop and manage a team of 2-4 Quality Control Operators, with a strong emphasis on training and right-first-time performance.
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Job Title: CMM Programmer Job Code: 10632 Job Location: Wilmington, MA Job Description: Responsible for performing inspections, tests and/or audits of purchased parts, units, materials, equipment, panel/module level assemblies and quality control programs to specifications.
Full-timeExpandApply NowActive JobUpdated 16 days ago - UpvoteDownvoteShare Job
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Author and review quality documents such as SOP, OOS/OOT, CAPA and Change Control originated internally as well as at the vendor sites. This individual will support method development, validation, and quality control activities conducted at Sarepta Andover in compliance with cGMP regulations.
$96,000 - $120,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Job Title: Quality Control Inspector. Quality Assurance function is responsible for ensuring the effectiveness and fulfillment of the client Quality Policy, which is to comply fully in the conduct of the Company's business with all applicable regulatory and customer required specifications, and to maintain an effective Quality Management System, working in partnership with the Operations and Engineering teams to ensure that products and processes confirm to applicable standards and specifications.
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Demonstrated experience in developing alpha radiopharmaceutical at an early stage in terms of radio synthesis and quality control development. Increase internal technical and operational capabilities to develop the radiochemistry platform focused on Pb212 including continuous monitoring, improvement and troubleshooting in the scope of radioprocess manufacturing, in process control including Radio-QC and release time.
Full-timeExpandApply NowActive JobUpdated 15 days ago - UpvoteDownvoteShare Job
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Acting as a one-man attachment to other special forces teams, these highly specialized Airmen are trained in a wide range of skills, including scuba, parachuting and snowmobiling, as well as being FAcertified air traffic controllers in order to establish air control and provide combat support on missions all over the globe.
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The QA Supervisor will manage the quality of raw material, in-process material and finished product, ensuring the existing product manufacturing procedures, GMP, HACCP, weight control and other quality control procedures are followed and are updated when necessary.
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quality control jobs Title: customer service in Reading, MA
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