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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.
$200,000 - $280,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Participates in product stage gate reviews representing Site Quality Assurance. Demonstrated experience building and leading exceptional Quality Assurance teams. Director, Quality Assurance Operations– CAR-T Manufacturing.
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A background of pharmaceutical manufacturing or quality control/quality assurance is a plus. Works closely with quality, manufacturing, Global Regulatory Affairs (GRA), and technical staff from global locations within industrial network, contract manufacturing organizations (CMOs), and alliance partners to author high quality Module 2 and 3 regulatory submissions for both development and post-approval dossiers.
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Their responsibilities include: Installing, testing, troubleshooting, repairing or replacing cryptologic networks, physical security systems, electronic equipment, antennas, personal computers, auxiliary equipment, digital and optical interfaces, and data systems Configuring, monitoring and evaluating Information Operations (IO), Information Warfare (IW) systems and Information Assurance (IA) operations Cryptologic Technician Collection (CTR) – CTRs serve as experts in intercepting signals.
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MS (or equiv) in CompSci, Information Systems Technologies - Information Assurance, Engg (Comp/Mech/Electronics), or related field, plus 3 years of experience in position involving similar duties/technical capabilities.
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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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As an Intern with McDermid Alpha Electronic Solutions you will support the Chemistry Department with general R&D operations and organizational tasks. Intern Personality Profile. Specific Intern Duties & Responsibilities.
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This position reports to the Associate Vice President, Quality Assurance and will manage or support: cGMP compliance assessment of contract manufacturers, the company SOP and Training systems, QA/QC Testing /Audit program, and Quality/Compliance decisions related to the Companys ANDA products, as well as its products subject to OTC Monographs and FDA or other industry-accepted standards for Dietary Supplements and Medical Foods.
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Lead the preparation and review of Uniform Federal Policy Quality Assurance Project Plans (UFP-QAPPs) for all projects. Maintain and implement the REAC Program Quality System. We are seeking an Environmental QA/QC Manager to support our U.S. EPA Response Engineering and Analytical Contract (REAC) and EPA Emergency Response Team (ERT.
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3-5 years of experience in drug safety, pharmacovigilance, quality assurance, or a related field. This role requires a strong leader with a deep understanding of commercial patient services, pharmacovigilance, quality assurance, and regulatory compliance.
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Manages the packaging Batch Record review and approval process with Quality Assurance and other CSO personnel. Works closely with Quality Assurance to obtain temperature excursion disposition to update impacted inventory in IRT and other related systems.
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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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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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Broad knowledge of risk-based quality systems approaches consistent with post-marketing Good Pharmacovigilance Practices and ICH E-6 for Good Clinical Practice. Facilitate and maintain a risk-based and scientific-based quality system to support Good Pharmacovigilance Practice (GVP.
$207,000 - $289,867 a yearFull-timeExpandApply NowActive JobUpdated 23 days ago - UpvoteDownvoteShare Job
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Job Description Description: Support in identifying cybersecurity deficiencies in information systems by performing technical assessments of assigned systems and applications to determine the severity of weaknesses; Supports the Security Authorization (SA) and Continuous Monitoring (CM), Risk Management Framework (RMF) process.
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assurance job Title: quality assurance intern in Warren, NJ
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