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Assist the Vice President Quality Assurance maintain a Reinsurance Claims Quality Assurance Program focused on assessing quality of technical claims handling, ensuring high quality claims handling for Everest, and identifying areas for improvement across the Global Reinsurance Claims Department.
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Reporting to the Executive Director of Development Quality Assurance, the Senior Director of Pharmacovigilance QA serves as a strategic partner managing quality and regulatory compliance related to Good Pharmacovigilance Practices (GVP) and other related activities performed by Drug Safety & Pharmacovigilance and Medical/Clinical Departments.
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Internationally, the position works cross-functionally with Logistics and Quality Assurance at Oticon Medical's suppliers to ensure that product labeling is consistent with FDA approvals.
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The Quality Assurance (QA) Automation Engineer designs, builds, tests, and deploys effective test automation solutions for a myriad of Web and Windows applications. This position will report to the Manager of IT Quality Assurance in the Information Technology department.
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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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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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Associates or no degree required with 4 or more years of experience working in the pharmaceutical industry in Quality Control/Assurance or Manufacturing, and 2 or more years in a leadership role.
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Reporting to the Global Quality Engineering Director, the Supplier Quality Specialist will achieve ALAM goals in the areas of manufacturing quality, technology advancement, productivity, off-spec elimination, non-conformance elimination, customer satisfaction, and cost reduction.
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Job Title: Lead - Quality Assurance. Gather application's business requirements and specifications for developing architecture pattern, formulating test plan & strategies, test analysis, test design, test cases, development & maintenance of database usingAzure DevOps, IBM Rational and Collibra Data Governance center, SharePoint, Data Modeling, & Oracle SQL Developer.
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Experience of working under own initiative and in planning and prioritizing workloads University or technical college degree or equivalent qualification in relevant sciences such as: Medicine, Pharmacy, Chemistry, Biochemistry, Biology, Microbiology, Biotechnology, Health Technology, Toxicology, Physics, Biophysics, Material Science Biomedical Engineering, Mechanical, Electrical or Electronic Engineering, Computer & Software Technology, Human Physiology, Nursing, Quality Management.
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Support Quality Systems such as; change control, deviation, CAPA, audits, quality metrics, etc. This role will be a hands-on resource reporting to the Quality Control Manager. We are seeking an innovative, creative, and detail-oriented Senior Quality Control Analyst to join our team in Bridgewater, New Jersey.
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Advise on and support the effective quality management of third parties, including SaaS / cloud suppliersLead risk assessment, quality assurance, quality/validation strategy definition and oversee their execution in collaboration with external service providersQuality Mgmt. SystemDefine Quality and Compliance Standards for emerging regulatory concerns relating to data science, artificial intelligence, machine learning, etc.
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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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The Quality technician provides constant supervision and support to the Pilot Plant while promoting a Food Safety culture on site. - Work with the Pilot Plant individuals on reporting quality deviations and taking immediate corrections.
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We are looking for a Quality Control Inspector interested in starting a SWEET career as part of our Quality Control team at PIM's Somerset site in New Jersey. Report food safety and quality problems to Plant Management and SQFP to initiate action.
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quality assurance jobs Company: Johnson in Raritan, NJ
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