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The Quality Assurance Case Aide (QAS4) is a practical and administrative support staff to the Community Umbrella Agency (CUA) program from within the Quality Assurance Department.
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The Quality Assurance Document Control individual acts as the primary liaison to our customer's quality assurance groups for batch record review and release. Job Description Quality Assurance Document Control Position Summary: Catalent Pharma Solutions is Philadelphia, PA is hiring for a Quality Assurance Document Control.
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Join our team and you will be able to provide insight and services that accelerate analytics, data integrity and quality increasing the reliability our clients reporting capabilities. Skilled at working with relational database management systems and SQL data transformation scripting Proven experience within the analytics domain gathering business and technical requirements, solution design, build, testing and solution deployment Strong technical writing skills and advanced data analytics knowledge Experience with business intelligence and data visualization and reporting platforms such as Tableau, Microsoft Power BI, Spotfire, etc.
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Overview WuXi Advanced Therapies is a leading global cell and gene therapy contract, testing, development, and manufacturing organization (CTDMO) that is dedicated to advancing the development and commercialization of cell and gene therapies.
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The primary purpose of the Manager, Quality Auditing Analyst is to provide leadership and direction of operational auditing for the following functions across the enterprise and covers approximately 1200+ associates: claims, contact center, enrollment, and provider maintenance.
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Required Education, Skills, and Knowledge Bachelor’s degree in a relevant discipline (biological sciences or equivalent)Minimum one (1) year of experience in the pharmaceutical industry within a Quality Control role; experience with cell therapy products is a plus.
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Conducts on-site provider visits, monitors Quality Improvement Plan submissions, and prepares required letters to providers. Essential Functions: Assists in the tracking and trending of all reported quality issues and produces trend analysis.
$59,600 - $66,000 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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5+ years of experience working with RDBMS (MySQL, Postgres, Teradata, etc.)
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Perform quality of care reviews on cases identified as Preventable Serious Adverse Events, based on the CMS / DPW Bulletin. Utilize the Healthcare Management integrated software system to build and track cases referred for quality of care, member complaints and PSAE's.
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Knowledge of Quality Management Systems (QMS). A South Jersey manufacturer has multiple openings for Quality Technicians for 2nd shift. These are full-time perm positions with benefits that begin on day1, competitive pay with bonus up to 10%, and OT pay when available.
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You’ll also be charged with mentoring fellow QC team members, performing GMP Quality investigations and QC stability testing. You'll be responsible for ensuring the highest standards of Quality Control Microbiology for life-saving therapies.
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Iovance is seeking an Associate Director, External Quality Control to provide strategic, technical, and operational leadership for external QC-related activities. Lead selection and oversight of contract QC laboratories including technical due diligence, routine performance management, and audits to ensure sustained quality analytical deliverables.
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The Coriell Institute for Medical Research is seeking an experienced Quality Assurance and Safety Manager to join our operational team. The person in this role will maintain all necessary documentation within the QMS including document control/document review, management review, audits, and corrective/preventative actions; perform all required internal quality audits and inspections including audit reporting to management; and complete in-house laboratory equipment calibrations as required.
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Review plans and procedures and assist with the implementation/utilization of Quality Assurance across the program. Candidate will ensure that the software quality records database, media, and supporting documentation are prepared and maintain in accordance documented requirements.
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The QA Supervisor will provide Quality Assurance support for the Quality Inspectors on the production floor, incoming material quality, and/or distribution quality, including quality oversight for material management of materials at Catalent-Philadelphia.
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Title: quality assurance Company: Intl Aids Vaccine in Philadelphia, PA
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