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Participates in Operating Room activities related to quality improvement, continuing education, orientation of new personnel and emergency preparedness. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment.
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Identifies performance improvement issues through chart review and attendance at morning report. Develops the quality improvement program of the Trauma Division in accordance with American College of Surgeon Committee on Trauma Guidelines.
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Duties include recruiting, supervising and evaluating all primary care providers and specialists, process improvement focused on clinical care, patient access, staffing, utilization management and patient scheduling, assisting in the development, implementation and monitoring of quality improvement and compliance efforts and budgeting and strategic planning.
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We also formed Blue Polymers, a joint venture with Ravago, to develop facilities that will further process plastic material from our Polymer Centers to help meet the growing demand for sustainable packaging.
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Along with the CLIA Lab Director and leadership, maintain laboratory audit readiness by overseeing and managing clinical lab audits with regulators, pharmaceutical partners, and with other agencies, ensuring that internal system and process audits are scheduled and conducted.
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The ideal candidate will have knowledge and experience in both non-profit accounting and cloud-based technology solutions along with an understanding of how to leverage technology for process improvement.
$82,400 - $156,200 a yearFull-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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The position focuses on process improvement related to clinical care, patient access, staffing, utilization management, and patient scheduling. Additional responsibilities include contributing to the development, implementation, and monitoring of quality improvement and compliance initiatives, as well as involvement in budgeting and strategic planning.
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Requirements Requires an advanced degree in Pharmaceutical Sciences, Chemistry, Materials Science, or related field with 5+ years of experience in process development and manufacturing of peptide and oligonucleotide APIs including PMOs. Experience with solid phase peptide/oligo synthesis preferred.
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Data Management: Maintain accurate records and data on community engagement activities, program outcomes, and client interactions, utilizing this information to inform decision-making and continuous improvement efforts.
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Our ideal candidate will have experience leading the people operations function for at least one globally distributed company and driving excellence in payroll, benefits, HRIS, compensation, policies, compliance, people analytics, and HR process improvement.
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Experience in project management and leading workstreams; execution of finance transformation, FP&A, and/or business process design/improvement initiatives. Demonstrable expertise in process improvement and operating/service delivery model design.
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Investment Operations generates operational alpha for Boston Partners and its clients through continuous process improvement. Reconciliation and Data IntegrityReview reconciliation between Northern Trust and custodians; act as escalation point for Northern Trust with any issues and maintain aging reportMaintain data integrity and security master requirements and interfaces between various internal systemsResponsible for start of day process by ensuring trading platform is ready and data exceptions are resolved.
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Collaborate with functional leads, including in vivo and in vitro, and discovery teams to drive program and candidate selection strategy and platform improvement. The Associate Director/Director, Oligonucleotide Medicinal Chemistry will oversee and actively contribute to all oligonucleotide medicinal chemistry activities from hit identification to clinical proof-of-concept.
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The Process Engineer is involved in new product scale-up, process optimization, technology transfer and process validation activities. Catalent Pharma Solutions is Chelsea, MA is hiring a Process Engineer who is responsible for assisting senior engineering staff in the design and implementation of manufacturing processes, instrumentation and equipment for clinical and commercial manufacturing.
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In particular, we are looking for individuals who can support current and emerging work across any number of areas such as: disability, population health, mental health and substance use, value-based purchasing and alternative payment models, measures of delivery and quality of services for beneficiaries, quality improvement, data analytics, and outcomes of innovative programs and policies.
$50,000 - $60,000 a yearFull-timeRemoteExpandApply NowActive JobUpdated Today
process improvement jobs Company: Ekidzcare in Boston, MA
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