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The Senior Manager also develops and establishes Quality Assurance testing methods with IT Operations, including automated regression test methods and tools using the golden dataset concept.
$175,000 - $195,000 a yearExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The Quality Assurance Manager will work under the direction of the Quality Assurance Director to perform the required quality assurance inspections on utility scale PV systems.
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The Quality Assurance Document Control Specialist role is an exempt position responsible for supporting the document management process within a cell therapy manufacturing facility to support both clinical and commercial requirements in a sterile GMP environment.
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Participates in departmental quality-assurance and safety activities for drug usage, infection control, and handling hazardous materials according to state/federal regulations and departmental policy; assists in the collection and review of patient-specific data used by pharmacists for monitoring drug therapy.
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Quality assurance, client experience and satisfaction. - Work closely with the Director of Nursing in supervising and mentoring our team of compassionate caregivers, ensuring they deliver high-quality care that meets the individual needs and preferences of each client.
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Global Pharmaceutical company, with US HQ in Central New Jersey, focused in Metabolics, Endocrinology and Oncology is expandingLooking for a strong Quality Assurance Manager for the entire North American manufacturing and quality organization.
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A background of pharmaceutical manufacturing or quality control/quality assurance is a plus. The CMC Regulatory Technical Writer II authors high quality Module 2 and 3 regulatory submissions for both development and post-approval dossiers, change controls and technical reports.
Full-timeExpandApply NowActive JobUpdated 12 days ago - UpvoteDownvoteShare Job
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The Client Regulatory Technical Writer II authors high quality Module 2 and 3 regulatory submissions for both development and post-approval dossiers, change controls and technical reports. He/she/they defines and manages the compilation of the documentation, required for the authoring by reaching out to appropriate internal/external functions such as quality, manufacturing, Global Regulatory Affairs (GRA), technical experts from global organizations locations or contract manufacturing organizations (CMOs), or alliance partners.
$40 - $50 an hourExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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It is preferable that the candidate has experience working in a cGMP manufacturing facility, quality assurance, manufacturing compliance, clinical quality, or cell therapy. Legend Biotech is seeking QA Document Control Specialist as part of the Quality team based in Raritan, NJ.
Full-timeExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Looking for a strong Quality Assurance Manager for the entire North American manufacturing and quality organization. In addition, this role will perform critical quality assurance activities such as Change Management, SOP Management, and Audit oversight.
Full-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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BS degree in Chemistry, Engineering, Life Science or related discipline and a minimum of 10 years of relevant Quality Assurance experience; advanced degree and a minimum of 8 years relevant experience required.
$171,000 - $239,667 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Additional Responsibilities - Supplier Quality Assurance. Previous technical experience should be in materials management and/or supplier quality activities associated with biotechnology manufacturing processes (large scale cell culture and purification processes.
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This is a multidisciplinary role & this individual will need the ability to interface with all levels of the organization, including Manufacturing, MS&T, Quality Assurance, QC, Process/Analytical Development, Supply Chain, Training, Engineering/Facilities, HS&E, and Finance.
$90,000 - $210,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Reporting to the Sr. Director of Clinical Quality Assurance, the Associate Director of Clinical Quality Assurance (CQA) serves as a CQA lead representative on the development team assuring quality and regulatory compliance related to GCPs and other related activities performed by Medical/Clinical Departments.
$139,000 - $195,200 a yearFull-timeExpandApply NowActive JobUpdated 12 days ago - UpvoteDownvoteShare Job
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The Quality Assurance Manager will play a key role for the North American manufacturing and quality organization, in managing activities related to Good Manufacturing Practices (GMP), in connection with CMOs and with the local RRD Inc. affiliate responsibilities.
Full-timeExpandApply NowActive JobUpdated 8 days ago
quality assurance jobs in Branchburg, NJ
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