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Alameda 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 SystemNevro
Redwood City, CA, United States
About Nevro: Nevro (NYSE: NVRO) is a global medical device company headquartered in Redwood City, California. We are focused on delivering comprehensive, life-changing solutions that continue to set the standard for enduring patient outcomes in chronic pain treatment. The company started with a simple mission to help more patients suffering from d
Job Source: NevroAlameda Health System
San Carlos, 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 SystemNevro
Redwood City
Regulatory Affairs Manager Company: Nevro Location: Redwood City, CA Position Type: Full Time Experience: See below Education: See below Regulatory Affairs Manager at Nevro in Redwood City, CA Req. Master�s deg in RA, Biomedical Eng�g or Med. Devi...
Job Source: NevroAscendis Pharma
Palo Alto, CA, United States
Here at Ascendis we pride ourselves in exceptional science, visionary leadership, skilled and passionate colleagues. We are a dynamic, fast-growing biopharma company with offices in Denmark, Germany, and the United States. Today, were advancing programs in Endocrinology Rare Disease, Oncology, and Ophthalmology. We are applying our TransCon technol
Job Source: Ascendis PharmaNevro
Redwood City, CA, United States
Regulatory Affairs Manager Read all the information about this opportunity carefully, then use the application button below to send your CV and application. Company: Nevro Location: Redwood City, CA Position Type: Full Time Experience: See below Education: See below Regulatory Affairs Manager at Nevro in Redwood City, CA Req. Masters deg in RA, B
Job Source: NevroAlameda 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 SystemNevro
San Carlos, CA, United States
Regulatory Affairs Manager Company: Nevro Location: Redwood City, CA Position Type: Full Time Experience: See below Education: See below Regulatory Affairs Manager at Nevro in Redwood City, CA Req. Masters deg in RA, Biomedical Engg or Med. Device Engg, & 6 years exp as RA Manager or RA Specialist or rel. occupation in RA, or Bachs deg in RA, Biome
Job Source: NevroNewark, 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
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Email Alert for Regulatory Affairs Manager jobs in Newark, CA, United States
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