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The Software Quality Assurance Testing Engineer will play a key role in the quality assurance of Anti-Money Laundering ("AML"), Sanctions Screening, AML Transaction Monitoring, and Know Your Customer ("KYC") suite of applications in the Boston, MA area.
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Associate Director, Clinical Quality Assurance / GCP QA will report directly to MorphoSys’ Group Leader GCP/GVP/GLP based in Germany and indirectly to MorphoSys’ Head of Global Quality Operations.
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The role works closely and have high visibility with Executives, VP's and Directors of Engineering, Infrastructure, SRE, Product Management and Customer Support to ensure overall software quality in development pipeline all the way to production regions, and to set the strategy for developing high-quality software to solve complex problems for our customers and users.
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The Quality Assurance Director will provide the Cell Manipulation Core Facility with direction and leadership in the development, implementation and auditing of Quality programs to support regulatory and accreditation compliance with applicable requirements (GMP/GTP/FACT/JC and other industry standards) as well as federal and state laws, and ensure that clinical and laboratory operations meet the highest quality standards set by the organization.
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Assists with all Quality Control/Quality Assurance processes as needed to ensure continuous compliance with State and Federal regulatory guidelines. The Breast Imaging Quality Navigator is responsible for maintaining the highest levels of empathy, communication, and efficiency to provide exemplary patient guidance and direction through complex imaging and treatment pathways.
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Quality Assurance: Ensure quality processes, procedures, and tools are fit for purpose, GxP compliant, and support analytical timelines and future commercial launch needs. Team Development: Build and lead an empowered team of quality and regulatory experts, overseeing tools, business processes, and procedures supporting cell-based bioassay, cell & gene therapy, and virology testing.
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Director of Rehab / Therapy Program Manager experience preferred. Director of Rehabilitation Qualifications. Director of Rehabilitation. Foster a service-oriented culture focused on top of license practice, collaboration, employee engagement, quality, patient safety, service excellence, fiscal responsibility, and the overall patient/resident experience.
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Perform secondary analyses to create additional value from Lilly’s data assets, create high quality data visualizations and present research findings to the scientific community. With high growth in this field, the Lilly Institute for Genetic Medicines is under construction, which will provide a state-of-the-art facility for the teams dedicated to developing innovative RNA, oligonucleotide, gene and genomic based therapeutic agents.
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Location: 258 Chestnut Street, Chelsea, MAPay Range: $20 to $23 per hourQUALIFICATIONSThe Kids Club Director (program administrator) shall be at least 21 years of age and meet one of the following sets of requirements:Have a minimum of a bachelor’s degree in child development, Early Childhood Education, Elementary Education, Child Guidance, Human Services, and Nursing.
$20 - $23Full-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Your role: The Director of Quality-RI is accountable for end-to-end quality across the product life cycle including new product introduction, sustaining & improvement engineering, risk management, post market surveillance, acquisitions and integrations, management of the Quality Management System (QMS) and quality key performance indicators assuring business quality & compliance.
$128,000 - $236,000 a yearFull-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Job Description: Director, Quant Data Engineering The Role The Asset Management Quant Research Engineering team is looking for a Director of Data Engineering who wishes to take on the challenge of building a world-class data operation.
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Act as a team lead and assist the Deputy Director of Safety Assurance and Promotion in managing, mentoring, and developing members of the Safety Assurance Team. The Safety Lead is responsible for assisting the Deputy Director of Safety Assurance and Promotion and the Director of SMS and Safety Oversight in designing, implementing, and monitoring the Authority's safety programs, policies, and procedures.
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Karuna is seeking an experienced and motivated individual to join our Quality Assurance team as Manager/Senior Manager, CMC Quality Assurance, to support drug development from Phase 1 to commercialization.
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Demonstrate the highest degree of professionalism, ethics, quality, and integrity. Develop content and lead the preparation of high quality, refined reports, written analyses, presentations, and other client deliverables.
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The ideal candidate will have a proven track record of leading and inspiring diverse teams, a keen interest in collaborating with in vivo scientists to generate high quality preclinical data, a passion for learning, strong communication and organizational skills, and a comprehensive understanding of the use of animal models in biopharmaceutical Research & Development.
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Title: director quality assurance Company: Sun Country Industries in Cambridge, MA
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