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The Quality Assurance Document Control (QADC) Associate Specialist supports the cGMP Document Control operations for the Client Cell Therapy Above-site organization, including the document approvals, document change control process, periodic review and system reporting.
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The Software Quality Assurance Engineer III will serve as a Quality representative in the Neuromodulation Software/Firmware product development. The Software Quality Assurance Engineer III will be involved in the development, testing and validation of Software/Firmware products.
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Ensure all corporate safety, quality control and quality assurance standards are met. Adhere to laboratory's quality control policies and document all quality control activities.
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Under general supervision, perform embedding and microtomy for select specimen types as defined by Histology Manager/Supervisor. Under general supervision, perform special stains under approval of/at discretion of Histology Manager/Supervisor.
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As a Microbiology Senior Scientist, you will be a member of Pfizer’s dedicated and highly effective quality assurance and control team. Experience dealing with Quality Operations and Quality Assurance.
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The Senior Quality Assurance Test Automation Analyst within Enterprise Systems Department (ESD) primary responsibility will be to build a test automation infrastructure and Framework that leverages DevSecOps, Continuous Integration/Continuous Delivery aspects and performing a variety of activities relating to various projects and production support for Georgia Tech Research Institute (GTRI.
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DCF Information Systems strives to improve continually improving technology services that are cost-effective and of the highest effectiveness and quality. SECURITY/PRIVACY CONSIDERATIONS: Comply with Vendor Qualification, DCF Child Protection Background Check, FBI Fingerprint Background Check and DCF Non-disclosure Agreement.
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Knowledge of cGMP, GxP, GAMP, and SDLC regulations, including 21CFR part 11 electronic records and electronic signatures, and good documentation practices with the ALCOA+ principles of data integrity, risk-based approaches to validation, Computer Software Assurance (CSA) principles.
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Liaise between engineering and quality assurance throughout validation lifecycle of packaging equipment and data historian network. Partner with quality assurance team to participate in internal and external audits to defend equipment validation packages including calibration and maintenance.
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The Cell Therapy Specialist will perform and/or verify all tasks associated with the manufacture of commercial product following batch records and standard operating procedures (SOPs) to ensure safe and compliant operations as well as works as part of a team to execute GMP runs in close collaboration with Materials Management, Quality Control and Quality Assurance.
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We’re looking for Quality Assurance Associates in our Fulfillment Center to inspect and ensure that all ingredients and all items in boxes meet required quality standards. The Quality Assurance Associate will assist with Gold Standard and table set up and audit tables and bins on a continuous basis (at least once an hour.
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Ensure quality assurance oversight and compliance to approved policies and regulations on laboratory computerized systems and instruments that conduct biological, chemical, and physical analyses on pharmaceutical products through all stages of the manufacturing process from incoming raw materials to finished goods, and environmental monitoring programs.
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Gathers and communicates quality metrics and performs periodic Quality Assurance audits. Ensures standard Quality Assurance processes are adhered to by the project team and provides feedback and guidance to the team on processes and deliverables.
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Job title: Quality Assurance Specialist. Specialist Quality Assurance position available on our Quality Team. Providing Quality support for vaccine, biologic, and sterile manufacturing processes through collaboration with Technical Operations and Operations.
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BS/MS with 6-10 years of experience in biotech/pharma or CRO in a nonclinical safety assessment organization or Quality Assurance group; PhD with 0-3+ years of applicable experience. Primary responsibility for the Scientist/Senior Scientist in NSE is to ensure timely and high-quality deliverables from NSE to meet client's Discovery and Development goals; these deliverables include management/coordination of contracts, study-related documentation (protocols/reports), and regulatory submission documents, and program-related documents (e.g., candidate nomination.
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quality assurance jobs Company: Integrated Resources Inc Iri
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