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Alameda Health System
Concord, CA, United States
Summary SUMMARY: Plans, coordinates, monitors compliance with federal, state and local regulations; manages accreditation activities necessary for maintaining required accreditation; manages requirements for certifications and licensure from various organizations, such as Joint Commission (JC), California Department of Public Health (CDPH), CMS, O
Job Source: Alameda Health SystemAlameda Health System
Dublin, CA, United States
Summary SUMMARY: Plans, coordinates, monitors compliance with federal, state and local regulations; manages accreditation activities necessary for maintaining required accreditation; manages requirements for certifications and licensure from various organizations, such as Joint Commission (JC), California Department of Public Health (CDPH), CMS, O
Job Source: Alameda Health SystemAlameda Health System
Castro Valley, CA, United States
Summary SUMMARY: Plans, coordinates, monitors compliance with federal, state and local regulations; manages accreditation activities necessary for maintaining required accreditation; manages requirements for certifications and licensure from various organizations, such as Joint Commission (JC), California Department of Public Health (CDPH), CMS, O
Job Source: Alameda Health SystemBD
Milpitas, CA, United States
Job Description Summary Job Description We are the makers of possible BD is one of the largest global medical technology companies in the world. Advancing the world of health is our Purpose, and it’s no small feat. It takes the imagination and passion of all of us—from design and engineering to the manufacturing and marketing of our billions of
Job Source: BDZEISS
Dublin, CA, United States
Employer: Carl Zeiss Meditec, Inc. Position: Senior Regulatory Affairs Specialist Duties: Works collaboratively with Global Regulatory Affairs, Product Development Teams and Product Marketing to register products in the United States. Additionally, this person supports and as appropriate develops pre-launch regulatory strategies, and facilitates
Job Source: ZEISSBayside Solutions
Fremont, CA, United States
Director, CMC Regulatory Affairs Direct Hire Full-Time Role Salary Range: $208,000 - $235,000 per year Location: Redwood City, CA - Hybrid Role Job Summary: The position is responsible for providing CMC regulatory strategies and leading the preparation of CMC sections of regulatory submissions to support the clinical development and eventual mark
Job Source: Bayside SolutionsArcus Biosciences
Hayward, CA, United States
Description Senior Manager, Regulatory Affairs CMC Summary: The Senior Manager, Regulatory Affairs CMC will provide support on a variety of activities in the Regulatory Affairs department related to regulatory submissions and systems. The individual must have the ability to work independently and as an effective and engaged team member in a fast
Job Source: Arcus BiosciencesStryker
Fremont
We are excited to be named one of the World’s Best Workplaces by Fortune Magazine! We are proud to offer you 12 paid holidays annually. For an overview of our benefits and time off, please follow this link to learn more:US Stryker employee benefits. (loudfront.net/oms/000000/document/2024/6/SMVZW\_USStrykerEmployeebenefits/USStrykerEmployeebenefits
Job Source: StrykerDublin, CA, United States
Summary
SUMMARY: Plans, coordinates, monitors compliance with federal, state and local regulations; manages accreditation activities necessary for maintaining required accreditation; manages requirements for certifications and licensure from various organizations, such as Joint Commission (JC), California Department of Public Health (CDPH), CMS, OSHPD, CDPH Lab Field Services, CDPH Radiologic Health Branch, etc.; prioritizes projects, coordinates action plans, and monitors/analyzes results for accreditation projects, consistent with the organization's strategic goals.
DUTIES & ESSENTIAL JOB FUNCTIONS: NOTE: Following are the duties performed by employees in this classification. However, employees may perform other related duties at an equivalent level. Not all duties listed are necessarily performed by each individual in the classification.
1. Actively coordinates the organizations readiness rounds program and is primarily responsible for the development, communication, implementation and tracking of action plans necessary to close identified gaps in care or compliance with The Joint- Commission (TJC) standards and Centers for Medicare and Medicaid Services (CMS) and Title 22 regulations.
2. Assists in all accreditation and regulatory activities, including surveys, survey preparation and readiness assessments.
3. Develops comprehensive accreditation work plans by establishing deliverables, accountabilities, and timelines.
4. Finalizes corrective action responses to The Joint Commission and other regulatory agencies for survey and for-cause and compliant investigations.
5. Identifies growth and areas of opportunity to enhance Regulatory Affairs and AHS initiatives.
6. Identifies regulatory vulnerabilities and determines escalation level if necessary.
7. Maintains and implements department unannounced survey plans.
8. Manages communications, agendas, and logistics for onsite survey activities.
9. Manages onsite accreditation and regulatory surveys; supports command center activities.
10. Performs other duties as assigned.
11. Provides guidance on Joint Commission standards interpretation and other regulatory requirements as they apply to organizational practice/ performance.
12. Serves as contact and point person for Joint Commission accreditation manuals, standards-related publications and newsletters and educational materials; distributes pertinent information.
MINIMUM QUALIFICATIONS :
Any combination of education and experience that would likely provide the required knowledge, skills and abilities as well as possession of any required licenses or certifications is qualifying.
Preferred Education: Masters degree in a healthcare related field.
Preferred Licenses/Certifications: Certified as a Professional Healthcare Quality (CPHQ) or Certified as a Joint Commission Professional (CJCP); LEAN/Six Sigma Certification.
Required Education: Bachelors degree in nursing or healthcare related field.
Required Experience: Five years of hospital operations or patient care experience; two years in accreditation/licensing/regulatory compliance/ quality/performance improvement/patient safety in healthcare; experience applying quality assurance/performance improvement (QAPI) and customer service approaches; experience with Midas, Epic / Electronic Health Record (EHR), County Health Systems, OSHPD.
Quality
Regulatory Affairs
Full Time
Day
Business Professional & IT
FTE: 1
Required Preferred Job Industries Other
Email Alert for Regulatory Affairs Manager jobs in Dublin, CA, United States
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