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

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/

Drafts, reviews, analyzes, and negotiates plan and provider templates, agreements, and memoranda and other legal documents. Coordinates, manages and provides strategic advice on the full spectrum of health plan, integrated care, and provider contracting issues for Payor Partnerships. Facilitate the coordination of input from various subject matter experts throughout the n

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

This is a full time (100% FTE), University Staff (non classified) Quality Assurance Coordinator position available at ClinImmune Cell & Gene Therapy within the Division of Allergy and Clinical Immunology at the University of Colorado Anschutz Medical Campus. ClinImmune provides umbilical cord blood and tissue banking, clinical testing for human stem cell and organ transpl

The Regulatory Affairs Coordinator is responsible for providing central management and regulatory oversight for clinical trials and investigator initiated studies for The Division of Gastroenterology and Hepatology. This position will work closely with Principal Investigators, Research Development Manager, the department's administration team, and other departments and ce

Station Engineer ID 2024 7053 Job Locations US CA Concord | US CO Denver | US GA Atlanta Category Professional Position Type Regular Full Time Job Description Take Your Engineering Career to the Next Level! Are you ready to be challenged, make a difference, and experience professional growth in your career? Our Engineering team is looking for you! Kleinfelder (KLF) provid

Exercise limited judgment on details of work and in application of standard methods for conventional work Demonstrate sound engineering judgment Move Forward with Kleinfelder Kleinfelder has been connecting great people to the best work since 1961. We are engineers, scientists, and construction professionals providing solutions that improve our clients' transportation, wa