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Own, Investigate, and document OOS test results and deviations, and investigations for cGMP Quality Control. Execute analytical quality control release, stability and complaint (follow-up) testing for raw materials, in-process and final products to ensure compliance with cGMPs, GLPs, GDPs, Quality Assurance Procedures, SOPs and established deadlines.
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This Opportunity allows for a lot of growth and ability to work with QC Chemistry practices! Chemistry, pH, FTIR, Karl fisher, titrations, solubility, Hplc, Wet chemistry, NMR, GCMs. Characterize organic and inorganic compounds with NMR, GCMS, HPLC, FTIR, and wet chemistry tests.
$50,000 - $60,000 a yearFull-timeExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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The QC Lab Manager (Shift) will be responsible for overseeing a testing laboratory charged with the execution of all GMP bioassay testing (release and stability) related to Sarepta's Gene Therapy pipeline.
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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.
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Oversee and continuously improve FDA / regulatory compliant Quality System for QC laboratory system. Perform review of release, stability, validation, analytical quality control tests on raw materials, in-processing and final products.
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Plan, direct and coordinate QC batch record review, logbook review, QC test review, and lot disposition activities. Serve as a leader within the QC group and as a knowledge resource (data review, electronic review, data integrity, GDP) within the company.
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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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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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Apply Advanced Product Quality Planning techniques such as Failure Mode Effects Analysis, control plans and Measurement System Analysis to evaluate the producibility of new products and stability of production processes.
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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.
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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. In the past decade, as the fields of proteomics and metabolomics have developed as leading techniques for determining biomarkers for disease presence, progression and the monitoring of therapeutic response, CIL has worked closely with industry leaders and researchers to provide the stable isotope-labeled tools needed for improved quantitation and qualification of complex biological systems.
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Our Global IT Audit Senior Manager plans manages, and delivers high-quality, complex audits of global programs, risk areas, or initiatives, working around complex technology and application environments and across different business processes.
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Must have working knowledge of tools & technical processes including identity & access management, database management; software development and quality assurance methodologies, change management, vulnerability management, penetration testing, data loss prevention, batch processing, business continuity/disaster recovery planning; enterprise architecture, telecommunications, data center operations, etc.
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This is a highly impactful role requiring a seasoned professional equipped with a keen understanding of supply chain management, quality control, and food safety standards. Enforcing strict compliance with safety (HACCP, OSHA), personnel, security, pest control, and shrink control policies.
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Develop control system architecture, select components, detail schematic diagrams and system documentation, program controllers (PLC, DCS, RTU), program process visualization (HMI/SCADA), develop databases for archiving/displaying historical system data, and implement/commission control systems at client facilities.
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quality control qc manager jobs Title: project manager in Andover, MA
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