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Alameda Health Sytem
Oakland, CA, United States
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, CD
Job Source: Alameda Health SytemAlameda 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
Oakland, 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,
Job Source: Alameda Health SystemAlameda Health System
Hercules, 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 SystemMastech Digital
Oakland, CA, United States
Position: HIM Director-Regulatory Affairs Manager Location: Oakland CA USA 94612 (5 days onsite) Duration: 12+ Months (Possibility to extend/Convert) Required Qualifications: ? Bachelor's degree with additional 10 years of progressively responsible experience managing quality compliance/assurance functions. Masters degree may substitute for two
Job Source: Mastech DigitalUltragenyx Pharmaceutical Inc.
Novato, CA, United States
Brisbane, CA; Novato, CA; Woburn, MA; or Remote- United States Why Join Us? Be a hero for our rare disease patients At Ultragenyx, we fundamentally believe that taking real impactful action to care for the needs of patients and our people is always the right thing to do.To achieve this goal, our vision is to lead the future of rare disease medicine
Job Source: Ultragenyx Pharmaceutical Inc.Intellectt Inc
Alameda, CA, United States
Hello, I Hope you are doing great. This is Bhanu from Intellectt INC; we’ve got an important role Regulatory Affairs Associate - Alameda, CA with one of our prestigious clients. Interested candidates can please send your updated resume at [email protected] Role: Regulatory Affairs Associate Location: Alameda, CA Duration: 12 Months S
Job Source: Intellectt IncBio-Rad Laboratories, Inc
Hercules, CA, United States
As part of our RA/QA team, you will provide coordination of the internal and external audit program for IVD medical device GMP facility for instruments, software and reagents within Clinical Diagnostic Group. You will also be responsible for facilitating the management of the quality management system audit program and reporting to management. Thi
Job Source: Bio-Rad Laboratories, IncPort Costa, 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 Port Costa, CA, United States
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