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The Program and Outreach Director is responsible for developing, leading and overseeing a resident centered activities and outreach program that promotes and integrates the Phoenix Senior Living philosophy to incorporate wellness in all aspects of the seniors' lives we serve.
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Leads quality assurance for both molecular genetics lab and cytogenetics lab. Serves as primary quality liaison to TPMG IT, LIS Support systems and KPIT for ongoing and new issues. Interacts with TPMG Regional Quality and Compliance.
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The Department of Pediatrics at the Oregon Health and Science University (OHSU) seeks a General Pediatrics Medical and Quality Director to oversee an outpatient clinic's operations, an educational program, quality, and value-based performance metrics.
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We are seeking a driven, hands-on experienced Director of Quality to join our team that specializes in engineered materials and coating solutions for semiconductor applications worldwide.
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Responsibility includes managing supply chain and incoming quality, and in-house manufacturing quality, integrated Supermicro product reliability and performance. Recommend to corporate quality office project plan and initiatives to promote product quality policy and control standards, and ensure effective implementation at operational levels, both in-house manufacturing factory sites and supply chain source.
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We are currently seeking a dynamic, highly motivated, and experienced individual for the position of Associate Director of GMP Quality Control, who oversees GMP compliance of manufacturing, testing and release activities for SMPA, its partners, contract testing laboratories, and suppliers of drug substances and drug products used for investigational clinical trials and/or commercial phases.
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Associate Director, GMP Quality Control. Experience working in more than one product area (e.g. solid oral dose, injectables, combination products), and therapeutic area (e.g. oncology, urology, regenerative medicine) within Quality Control a plus.
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Advanced knowledge and use of software applications, including LC chromatographic analyses, statistical applications, and quality management systems (e.g. Veeva). The Associate Director ensures compliance with GMPs, SMPA procedures and applicable global Regulatory guidelines by providing oversight and management of the global contract testing laboratories in partnership with the Company's CMC Team. The Associate Director also participates in drafting and reviewing CMC sections of the IND, IMPD and BLA/NDA submissions.
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Review and approve Quality Events, Investigations, CAPA, Change Controls, and Complaints in eQMS. Contribute to product development by making recommendations for manufacturing controls, sampling and testing to ensure product quality and compliance with GMPs from development through commercialization.
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Participate, as needed, in audits of contract laboratory sites and support annual Risk Assessments as part of the Supplier Quality program. Experience in evolving GMP related quality systems, policies, and procedures to ensure compliance with evolving standards as well as improving the efficiency of related workflows.
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MercyOne Clive Rehabilitation Hospital strives to maximize the health, function, and quality of life of those we serve through comprehensive physical medicine and rehabilitation programs. Certification preferred by APIC (American Practitioners of Infection Control), and NAHCQ (National Association of Health Care Quality.
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Quality leader and quality culture promoter within the global organization. Responsible for compliance with regulatory filings and therefore must have experience in a Quality Assurance and/or Quality Control function for marketed pharmaceutical products or clinical trial materials.
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8+ years of experience required, with relevant experience in biotech or pharmaceutical industry with most experience in a Quality role. Expertise in design of method validation, transfer, and stability studies consistent with regulatory, quality, and pharmaceutical best practices (e.g., USP, ICH.
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The Director, Quality Assurance, will manage a GLP QAU, including Good Laboratory Practice / Good Manufacturing Practice (GLP/GMP) within the Gene Therapy Program (GTP) at the University of Pennsylvania, supporting the development, manufacture, and testing of viral vectors for clinical trials.
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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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Title: director quality Company: Phillips Medisize Magnesium Molding
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