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Reporting to the Senior Director, Analytical Development & Quality Control (QC), the Associate Director of Quality Control will be acting as QC lead, responsible for leading and managing the QC activities of PepGen’s pipeline.
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Develop collaborative relationships with peers in DTE, Market Access, Commercial, Quality, Vendor partners, and various other teams to help design, develop, enhance, and deliver solutions that meet business goals and objectives.
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Advanced knowledge of factoring and asset-based lending, accounting, statistical analysis, audit procedures, collateral, loans, and credit quality. Analyze the quality and accuracy of a borrower's books, records, and financial and collateral reports submitted to the bank.
$210,000 a yearFull-timeExpandApply NowActive JobUpdated 19 days ago - UpvoteDownvoteShare Job
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The Associate Director, Clinical Data Analyst, has a critical role in the delivery of high-quality external data across Dyne's development pipeline by proactively identifying, measuring, and mitigating risk prior to acquisition of non-electronic data capture (EDC) data.
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Competitive Salary Annual Bonus Equity (RSUs) 401k Program REMOTE Health Benefits Commercial DrugJob DetailsWe are looking for an Associate Director of Quality Operations who will provide laboratory QA support for our biologics commercial and clinical development programs by working closely with our various contract development and manufacturing organizations.
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We are looking for an Associate Director, Strategy and Operations to work directly with our Chief Operating Officer (COO) to drive the company’s growth and operations, including the operations of the clinical diagnostics laboratory.
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Acts as central steward of data quality, monitors risks through the holistic review of clinical and operational data, using detailed knowledge of the protocol, considering the specific therapeutic area aspects of the protocol related to the data collected and aligning with cross functional operational plans to drive comprehensive data science modeling tasks.
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The Senior Manager/Associate Director, Supply Chain Planning will be responsible for supply chain planning for clinical supplies (clinical trial material) across a number of small molecule drug development programs in support of Xenon’s clinical trials.
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Attends/covers for the Executive Director at hospital meetings as needed such as but not limited to; OIC, Quality & Safety, EOC, Data & Privacy and Diversity. The Associate director provides administrative oversight primarily when the Executive Director is off campus or off.
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A Third Rock Ventures Stealth NewCo is seeking a Senior Manager/Associate Director, Quality Control (QC) to join their growing, experienced, and collaborative CMC team. Senior Manager/Associate Director, Quality Control (QC.
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This individual will report to the Sr. Director of Global GCP/GLP compliance and while working closely with the US Site VP and the Global Quality team. Minimum of 5+ years of progressive Quality experience working in regulated environment preferably in the field of biotechnology, biopharma, and/or cell/gene therapy (deep experience with GLP or GCP preferred.
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Tango has an exciting new opportunity to join our growing IT team as an Associate Director of Business Systems. Oversee master data management systems and tools, supporting broader data governance efforts to drive data quality.
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Promote advances in healthcare delivery science and digital medicine to improve population healthThe Director will work with UMass Chan-Lahey researchers and clinicians to harness innovations in healthcare delivery science to tackle prevalent health challenges and enhance the quality of care across diverse populations.
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In addition, the Associate Director will provide essential medical and scientific expertise, review, advisement and oversight to support development of high quality promotional and medical materials, internal training materials, and communications as part of the Promotional Review Committee (PRC) and Medical Review Committee (MRC.
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The Associate Director is a key member of multidisciplinary teams responsible for preparation of high-quality regulatory submissions focusing on chemistry, manufacturing, and controls (CMC) for lifecycle management and global expansions of the commercial programs.
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quality director jobs Title: associate in Everett, MA
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