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CSV, computer system validation, software, computer systems, GMP, good manufacturing practice, cGMP, current good manufacturing practice, vendor validations, Quality assurance, QA, GAMP, validation, validation plan, validation protocol, master validation schedule, GLP, good laboratory practice, CSV engineer, computer validation specialist, hybrid, biotech, biopharma, pharmaceutical, IQ, OQ, PQ, LIMS, QMS, quality management system, EDM, validation.
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Minimum of 10-years as Quality Control (QC) or Quality Assurance (QA) Inspector of structural steel or pipe manufacturing or heavy-construction where two (2) of the ten (10) years were spent as a Quality Assurance (QA) Inspector is preferred.
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The QA Senior Documentation Specialist will be responsible for documentation generation and the maintenance of documentation systems. As QA Senior Documentation Specialist, you will be joining an organization where people of all backgrounds and experiences are respected, and where we work together focused on changing lives.
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The QA Operations Specialist II will join the Civica, Inc. ("Civica") organization and its newly forming team at the Petersburg, Virginia site by bringing their knowledge and experience in service to patients and pursuit of excellence in quality and compliance.
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The Sr. QA Specialist for QA Material and Site Compliance will perform specialized level work assignments regarding material Quality Systems, general Quality projects, and change control as it relates to Material and Site Systems.
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Innova Solutions is immediately hiring for a QA Associate Specialist - Document Control. Tittle : QA Associate Specialist - Document Control. As a(n) QA Associate Specialist - Document Control.
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Partner with local QA/QE to evaluate and test new upgrades/ patches to Operating Systems/ applications and write install instruction for Lab/MFG managed services support personnel. Administer updates on QC/ Manufacturing instruments/ systems such as user additions, removal, method/ assay updates.
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Experience in food manufacturing, food science, QC/QA, or co-op or internship. Ability to become the plant Proficy implementation specialist with the goal of the integration of operational data collection for analysis.
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The Quality Assurance Specialist position plays a key role in supporting the cGMP quality operations for the Bothell Manufacturing Plant (Jump). The primary focus of the QA Specialist role will be to support routine clinical and commercial production to ensure consistent compliance with regulatory and industry expectations.
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Our client Medical device manufacturing QA Specialist III is seeking a to join their team. QA Specialist III. - Quality Experience working in pharma, medical device or related life sciences industry with cGMP / GDP manufacturing environment preferred.
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Quality direction and setting quality expectations for construction quality activities and supporting the efforts throughout the execution, start-up and commissioning including assuring the expectations are achieved and having functional responsibility for QC execution via the Site QA/QC Manager(s.
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Gmp, pharmaceutical manufacturing, quality investigation, cGMP, Deviation, complaint management. Minimum of 3 - 4 years experience with knowledge and understanding of regulatory compliance / cGMP requirements for pharmaceutical manufacturing processes / operations.
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The QA Specialist conducts QA audits of BIO laboratories and functions including but not limited to ongoing process, data review audits, technical report, and study independent facility / process.
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Provide QA (Quality Assurance) review and approval of Quality method validation/ QC equipment qualification, QC protocol, reports, QC process control document, new and existing procedures, and Quality Control deviation/investigations.
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An working understanding of food manufacturing acronyms (SQF, QA/QC, CQP, QAP, HACCP, SOP,5S, GMP, etc.) The technician will provide adequate information and notification to the QA Supervisor through the daily line check sheet in an accurate and timely fashion to ensure the safety and quality of all product being packaged.
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