The position provides both management oversight and hands on support and implementation of safety programs for EMCOR Facilities Services, Inc., (EFS) primarily at client location in Golden, CO. The primary purpose of this role is to support the site teams in their execution of the EFS safety program. The position requires the ability to communicate effectively and efficie

Posted Apr 26, 2024 Weekly Hours 40 Role Number 200547914 Imagine what you could do here. At Apple, new ideas have a way of becoming extraordinary products, services, and customer experiences very quickly. Bring passion and dedication to your job and there's no telling what you could accomplish. The people here at Apple don't just create products they create the kind of w

At Nutrien, our purpose is Feeding the Future and we do so with safety, inclusion, integrity and results as our core values. Nothing is more important than sending our people home safe, every day. Nutrien Ag Solutions is the retail division of Nutrien, the largest crop inputs company in the world. As part of our collective mission of Feeding the Future, Nutrien Ag Solutio

Reviews prime contract and subcontract details for specifications and requirements, identifies quality requirements and ensures that quality activities align with project scope as per the terms and conditions. Performs visual examination, witnesses, monitors, and documents results as per project specifications and Inspection testing plans (ITPs). Collects and compiles qua

Perform field and/or laboratory testing, observation, and inspection of construction materials (e.g. soils, aggregates, concrete, asphalt, and steel). Communicate with project manager, engineering technicians, client representative, contractor's representative and others as applicable regarding the construction site, project requirements, and testing, observation, and ins

The Director of Design Quality Product Lifecycle Excellence will direct all Quality Management System related activities for Research & Development, Risk Management, and Product Lifecycle Management. As a member of the Global Quality leadership team, the Director will play an integral role in designing and implementing quality systems to support the successful development

Troubleshooting network equipment, removing/replacing defective equipment, and working with appropriate resources to isolate and ultimately restore the network. Analyzing blueprints to determine where construction projects will take place. Identifying and mapping location and depth of utilities such as water, sewer, gas, cable, oil and electric lines. Documenting interact

include influencing and driving teams in the areas of process improvements, trend monitoring and correlating leading quality metrics, problem solving approaches, and data analysis. Leads root cause analysis of complex systems issues. Evaluates changes to products ensuring that the implications of changes are fully understood. Leads Management Review for factory that drives

Requisition ID 31924 At Terumo Blood and Cell Technologies, our 7,000+ global associates proud to come to work each day, knowing that what we do impacts the lives of patients around the world. We make medical devices and related products that are used to collect, separate, manufacture and process various components of blood and cells. With our innovative technologies and

A. HMIS System Oversight and Support Provide technical assistance (group and individual user consultation) and data entry oversight to HMIS end users to enhance data quality and program performance. Collaborate and coordinate with program staff on HMIS program set up, data entry, analysis, and reporting. Promote the use of HMIS and reporting accountability throughout DMSS

Supervise and provide direction to quality assurance technicians/auditors who are responsible for enforcing good manufacturing practices and other quality related policies in order to meet product quality standards. Review Production Records and other manufacturing related documents to verify compliance and record keeping for all mandated manufacturing processes, quality

Serve as legal regulatory counsel and strategic partner to DaVita Labs, with a primary emphasis on healthcare laws and regulations, as well as support for payor relations and contracting. In partnership with other DaVita attorneys and compliance teammates, assist business clients in identifying and resolving legal/regulatory matters related to business initiatives. Advise

include but are not limited to Design, Implement, and improve engineering and program Lifecyle management policies, procedures, and standards to be used for Test and Flight Operations systems. Manage data in Blue Origin eco system Establish effective communication with major stakeholders. Lead and/or support change control meetings to ensure risks and change impacts are we

Support Credentialing Team who is responsible for reviewing all applications submitted by providers to DaVita to be credentialed in our facilities. Identify and opine on elements that may be associated with increased risk to DaVita. Assist in updating medical staff bylaws. Provide legal guidance related to peer review investigations. Develop policies and process related t

High school diploma or equivalent required. Must possess the ability to communicate and interact positively with others who are in a time of need. Experience working in a high volume environment preferred. Experience working with the homeless population or experience in a related direct human services field working with underserved population preferred. Gain/Maintain CPR/