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What does a successful Commerce Hub Quality Assurance Engineering Director do at Fiserv? Commerce Hub Quality Assurance Engineering Director opportunity is to ensure, that the delivery is of the best quality, predictable and consistent.
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Reporting directly to the Senior Manager of Quality, this position collaborates closely with External Manufacturing Organizations (EMO), spanning pharmaceuticals, medical devices/combination products, consumer products/OTC, and biologics sectors, ensuring adherence to cGMP regulations and Bausch Health requirements.
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Responsibilities will vary depending on department of assignment (e.g., Emergency Room/Clinic, advisory to non-medical administrator, infection control, nurse/health education development, quality assurance, nurse anesthetist, etc.
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Minimum of 9+years' experience in validation, biological quality assurance and/or quality control in an FDregulated biotechnology or pharmaceutical company with progressive levels of responsibility.
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Must have experience collaborating with other teams such as Regulatory Affairs, Clinical Development, Quality Assurance, Legal, Clinical Operations, etc. The successful candidate will provide quality expertise to manage and improve processes across Aquestive's development program, ensuring compliance with Good Clinical Practices (GCP), Good Laboratory Practice (GLP), Preclinical stage and GMP for clinical manufacturing oversight.
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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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The purpose of the Facility and Reliability Engineer is to development and implement a Reliability Centered Maintenance (RCM) strategy to support Summit West Cell Therapy Operations and to maintain a qualified and compliant facility operation status.
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The Senior Scientist, Quality Control Analytics will coordinate and execute all activities to ensure the timely testing and release of all samples, collaborate with team in the design and execution of validation and other major projects.
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The Specialist will partner with site Business Owners, CI Owners, Quality, and the global EMES team to create, manage, and improve computerized systems/Recipes validation deliverables for electronic systems, applications, and associated controls to maintain data integrity supporting ALCOA+ principles throughout the CSV lifecycle.
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Hiring for Quality Assurance Engineer Consultant (Must-Have Skillset: ETL Testing, Data Driven Testing, Enterprise Data Warehouse Testing) role. Minimum 8 years of Quality Assurance experience (manual/automated testing) with a proven track record of improving Data Quality by implementing QA best practices within the organization.
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Use Mastercam CAD/CAM software to define efficient tooling operations to create high quality parts. The CNC Machinist Programmer will be responsible for operating several CNC machining tools to produce a variety of precision parts to support our growing sales of industrial drying equipment and systems.
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Description Department: Radiation OncologyLocation: Berkeley Heights, Florham Park and Clifton NJ*Accepting resumes with certifications in process*Job functions:Acceptance/Commissioning of radiation therapy machines/software/equipmentContinuous quality assurance and dosimetry calibration of various equipment, external beam radiation, brachytherapy, CT simulator and Treatment Planning System.
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Experience with MES infrastructure, ALM and Veeva document/change management systems and middleware WebMethods. The Specialist works cross-functionally to execute validation activities and prepare validation deliverables for S12 Enterprise Manufacturing Execution System (EMES) used in cell therapy manufacturing.
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As an Appliance Repair Technician, you are the key component in providing excellent customer service by providing high-quality maintenance services for our customer's appliances. Quality of Work: This role requires critical thinking skills and the ability to problem solve.
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Title: Validation - Specialist, MSEO Manufacturing Systems Validation. Familiar with the development of CSV documentation (Validation Plans, Requirements, Design / Configuration Specifications, Test Scripts [IQ/OQ/PQ/UAT], Summary Reports, Trace Matrices, SOPs.
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quality assurance jobs Title: quality assurance intern in Basking Ridge, NJ
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