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Analytical Development (AD) representative for cross function meetings/projects with manufacturing, Quality Assurance (QA), Regulatory Affairs and external partners. Support process development, setting of specifications, and chemistry manufacturing and control (CMC) regulatory filings and responses.
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Job Summary Job Description • Serves as a key contributor to understanding process effects on diverse materials used in high volume electronics manufacturing, via analysis work conducted in the Quality Assurance and Reliability Analytical Lab. • Works with a multi-disciplinary team of engineers to identify and understand physics of failure and failure mechanisms, while issuing and advising corrective actions and recommendations.
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The Quality Manager (textile/leather manufacturing) will lead Quality Assurance efforts by identifying key quality factors, coordinating teams to implement preventative measures, and ensuring product consistency through process validation and corrective actions.
$140,000 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Innova Solutions is immediately hiring for a Quality Assurance Associate. You will be responsible for providing Quality Assurance support to GMP clinical manufacturing. You will be a member of Client's dedicated and highly effective quality assurance team.
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As an individual member of the team, you will do various types of work, including running high-speed machinery, troubleshooting process problems, performing preventive maintenance on equipment, performing quality checks, and leading continual improvements in your area of ownership.
$26.98 - $53.65 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Functional support groups include Quality Assurance, Quality Control, Validation, Tech Transfer, and Quality Engineering. Consults with others to ensure quality of judgment.
$20.69 an hourExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Process Development Technician. Learns to identify process issues. 1-wk Tuesday/Wednesday/Saturday/Sunday - 2-wk: Monday/Thursday/Friday 2-pm - 2am. The incumbent will be required to solve problems regarding site assessment, specific units used in Biopharmaceutical manufacturing.
$21 an hourExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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1-wk Tuesday/Wednesday/Saturday/Sunday - 2-wk: Monday/Thursday/Friday. Manufacturing experience in a Good Manufacturing Practices (cGMP) or another regulated environment. Requires the moving of heavy equipment and the ability to lift :50 pounds.
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Tasks may be embedded in Standard Operating Procedures, operational and technical work practices and guidelines. Basic understanding of Good Manufacturing Practices (GMP). Significant reliance on supervisor.
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Job Title: Process Development Technician. Learns to identify process issues Innovation and Risk-Taking. Consults with others to ensure quality of judgment Direction Received. Job Title: Process Development Technician.
$21.42 an hourExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Quality certifications (ASQ, Lead Auditor). Continuous Improvement: Lead initiatives to enhance Quality Management Systems and enforce cGMP standards. Experience with Class II/III medical devices and manufacturing process tools (FMEA, Risk Management, Process Validation.
$130,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Identify new strategies, efficiencies and standards to streamline and improve the quality assurance process. Assist in planning, designing and executing quality assurance testing within the Credit Union, including the care and maintenance of a test script library.
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The individual in this role will work collaboratively with the analytical development team, quality control, and quality assurance to transfer and validate next generation analytical procedures for the testing of viral vectors, cell banks and gene therapy products in support of Genezen's services and commercial products in compliance with company policies and procedures and regulatory guidelines.
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You will make sure that product and process documents match the specificat QA, 2nd Shift, Specialist, Senior, Quality Assurance, Operations, Technology. You will be a member of Pfizers dedicated and highly effective quality assurance team.
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The scope of the quality department includes Program Quality engineering, Non destructive test lab, incoming and in process inspection, calibration and internal auditing in support of the entire Quality Management System.
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quality process assurance jobs in Wilmington, MA
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