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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. 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.
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This role manages technical quality assurance, oversees manufacturing QA/QC practices, conducts inspections, and coordinates supplier audits, requiring expertise in GD&T, SPC, and strong communication.
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Job Overview: This role, for a Document QC Specialist Contractor, will manage the quality control of scientific documents and Bioanalytical data for the Translational DMPK and Clinical Pharmacology group.
Full-timeExpandApply NowActive JobUpdated 26 days ago - UpvoteDownvoteShare Job
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Quality Control, HPLC, GC, UVVIS, Empower, Tech Transfer, Lab Equipment, LIMS, Method Validation. Support QC laboratory efforts and write protocols and SOPs for HPLC, GC, UVVIS, Etc.
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Experience in the following areas preferred: QC Lab Systems, Quality Management Systems & Document Management, Quality Assurance, Computer Systems Validation, GxP, Validated Change Control and Product Life Cycle Management.
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Perform release, stability, validation and complaint (follow-up) analytical quality control tests and assays on raw materials, in-processing and final products Following GLPs. Performs various quality control tests on raw materials, in-process and final product using approved test methods, Standard Operating Procedures (SOPs) and works in accordance with current Good Manufacturing Practices (cGMPs.
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Cambridge Isotope Laboratories, Inc. (CIL) is searching for a Quality Control Analyst I based onsite in our Andover, MA facility. One or more years of industry laboratory experience with GC, GC/MS, NMR or HPLC experience required; QC experience preferred, GMP experience a plus.
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The Quality Control Scientist I position is an integral member of the Quality Control team. Performs tasks related to QC functional responsibilities such as stability, validations, sample retention program, customer complaints, inventory maintenance, and continuous improvement efforts.
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We are seeking a bright, energetic and detail-oriented individual to join our team as a Quality Control Associate. Support new process development and continuous improvement by integrating QC tools and techniques.
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Asymchem Boston Corporation is seeking highly self-motivated candidates for QC Scientist/Senior Scientist to join the team in Woburn, MA. The successful candidate will possess an in-depth knowledge of quality control, cGMP and analytical science, to support drug substance development and ensure cGMP compliant practices in the QC laboratory.
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The Quality Control Manager organizes department workflow, coordinating daily activities of the lab while interacting with the Production Supervisor and other departments to manage priorities.
$95,000 - $120,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Geometric Dimension and Tolerancing (GD&T), Reading engineering prints, technical reports, raw material specifications, acceptance test Reports, Quality Assurance Inspection of Received Goods, Measuring Gauges / CMMs / Micrometers, Height / Plug / Thread gauges, Go / No-Go gauges, Statistical Process Control (SPC.
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Provide scientific support and apply technical expertise to the QC Tech Group laboratory department as well as other functional areas within the organization to ensure quality, compliance and efficiency in QC laboratory performance.
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Maintain, calibrate, and operate instrumentation in the QC laboratory. 0-2 years of QC analytical experience. Eurofins is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations.
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A Testing and Quality Assurance is needed for an American defense, aviation, information technology, and biomedical research company in the Tewksbury, MA area. Provide QA support, implement QA/QC practices into manufacturing process.
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quality control qc jobs Title: quality in Wilmington, MA
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