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Regulatory affairs associate Jobs in Oakland, CA

Last updated: 13 hours ago
  • Promoted
Regulatory Affairs Manager

Regulatory Affairs Manager

Alameda Health SystemOAKLAND, US
Full-time
Plans, coordinates, monitors compliance with federal, state and local regulations; manages accreditation activities necessary for maintaining required accreditation. manages requirements for certif...Show moreLast updated: 2 days ago
  • Promoted
Regulatory Affairs Director

Regulatory Affairs Director

Biolink360San Francisco, CA, US
Full-time
Director of Regulatory Affairs - San Francisco.We are seeking a highly motivated and experienced Senior Director of Regulatory Affairs for a Medical Device Orthopedic Portfolio.This person will lea...Show moreLast updated: 9 days ago
  • Promoted
DIRECTOR, REGULATORY AFFAIRS

DIRECTOR, REGULATORY AFFAIRS

Revolution MedicinesCA, United States
$204,000.00–$255,000.00 yearly
Full-time
Revolution Medicines is a clinical-stage precision oncology company focused on developing novel targeted therapies to inhibit frontier targets in RAS-addicted cancers. The company's R&D pipeline com...Show moreLast updated: 1 day ago
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Associate Director Regulatory Affairs APAC - Diabetes Care

Associate Director Regulatory Affairs APAC - Diabetes Care

Abbott Laboratories companyAlameda, CA, United States
Full-time
Abbott is a global healthcare leader that helps people live more fully at all stages of life.Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses an...Show moreLast updated: 23 days ago
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  • New!
Organic Regulatory Affairs Manager

Organic Regulatory Affairs Manager

NitricitySan Francisco, CA, US
$110,000.00–$135,000.00 yearly
Full-time
Nitricity is a startup addressing one of the most significant climate change contributors, and we seek your help.We are innovating in an essential chemical industry that supports global food system...Show moreLast updated: 13 hours ago
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Senior Director, Regulatory Affairs

Senior Director, Regulatory Affairs

Marea TherapeuticsSan Francisco, CA, US
$215,000.00–$285,000.00 yearly
Full-time
Marea Therapeutics is a clinical-stage biotechnology company based in San Francisco with a growing pipeline of first-in-class therapies to address genetically validated cardioendocrine disease targ...Show moreLast updated: 1 day ago
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Senior Director, Regulatory Affairs

Senior Director, Regulatory Affairs

Shelby American, Inc.San Francisco, CA, US
$215,000.00–$285,000.00 yearly
Full-time
All Jobs > Senior Director, Regulatory Affairs.Marea Therapeutics is a clinical-stage biotechnology company based in San Francisco with a growing pipeline of first-in-class therapies to address ...Show moreLast updated: 9 days ago
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Regulatory Affairs Associate

Regulatory Affairs Associate

Select Source InternationalAlameda, CA, United States
Full-time
Minimum of 2 years experience in a regulated industry (e.Regulatory area is preferred but may consider quality assurance research and development / support scientific affairs operations or related ar...Show moreLast updated: 2 days ago
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(Associate) Director / Senior Director, Regulatory Affairs, Therapeutics

(Associate) Director / Senior Director, Regulatory Affairs, Therapeutics

Mammoth BiosciencesBrisbane, CA, United States
$205,000.00–$260,000.00 yearly
Full-time
Mammoth is hiring a(n) (Associate) Director / Sr.Director, Regulatory Affairs, Therapeutics, to lead the regulatory activities of our growing CRISPR-based therapeutic programs as we bring them from c...Show moreLast updated: 18 days ago
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Vice President Regulatory Affairs

Vice President Regulatory Affairs

MeetSan Francisco, CA, United States
Full-time
Vice President, Regulatory Affairs.Hybrid Workstyle (2-3x per week onsite in South San Francisco, CA).Meet has partnered with an exciting biotech that is looking for a Vice President of Regulatory ...Show moreLast updated: 4 days ago
  • Promoted
Director, Clinical Regulatory Affairs

Director, Clinical Regulatory Affairs

Vera TherapeuticsBrisbane, CA, US
$180,000.00–$235,000.00 yearly
Full-time
Title : Director, Clinical Regulatory Affairs.Vera Therapeutics (Nasdaq : VERA), is a late clinical-stage biotechnology company focused on developing treatments for serious immunological diseases.Ver...Show moreLast updated: 1 day ago
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Organic Regulatory Affairs Manager

Organic Regulatory Affairs Manager

Tbwa Chiat / Day IncSan Francisco, CA, US
$110,000.00–$135,000.00 yearly
Full-time
Nitricity is a startup addressing one of the most significant climate change contributors, and we seek your help.We are innovating in an essential chemical industry that supports global food system...Show moreLast updated: 3 days ago
  • Promoted
Associate Counsel, Regulatory Affairs

Associate Counsel, Regulatory Affairs

VisaSan Francisco, CA, US
$152,900.00–$195,000.00 yearly
Full-time
Visa is a world leader in payments and technology, with over 259 billion payments transactions flowing safely between consumers, merchants, financial institutions, and government entities in more t...Show moreLast updated: 4 days ago
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  • New!
Regulatory Affairs Associate

Regulatory Affairs Associate

VirtualVocationsOakland, California, United States
Full-time
A company is looking for a Regulatory Affairs Associate.Key ResponsibilitiesProvide daily regulatory support to achieve organizational goals and strategiesSupport third-party certification processe...Show moreLast updated: 15 hours ago
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Regulatory Affairs Manager

Regulatory Affairs Manager

Randstad Life Sciences USSan Francisco, CA, US
$54.00–$63.00 hourly
Full-time
Get AI-powered advice on this job and more exclusive features.Randstad Life Sciences US provided pay range.This range is provided by Randstad Life Sciences US. Your actual pay will be based on your ...Show moreLast updated: 3 days ago
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Manager, Regulatory Affairs

Manager, Regulatory Affairs

Kyverna TherapeuticsEmeryville, CA, US
Full-time
Kyverna Therapeutics is a patient-centered, clinical-stage biopharmaceutical company focused on developing cell therapies for patients suffering from autoimmune diseases. The Kyverna therapeutic pla...Show moreLast updated: 1 day ago
Regulatory Affairs Associate

Regulatory Affairs Associate

ExelixisAlameda, CA
$70,000.00–$99,000.00 yearly
Full-time
Responsible for managing and maintaining existing investigational new drug (IND) and clinical trial application (CTA) submissions and preparing amendments in compliance with guidelines and regulati...Show moreLast updated: 30+ days ago
Regulatory Affairs

Regulatory Affairs

Katalyst HealthCares & Life SciencesOakland, CA
Responsibilities and Requirements : .This role will be accountable for leading the development and execution of innovative and value-added global regulatory strategies. Be responsible for formulating ...Show moreLast updated: 30+ days ago
  • Promoted
Regulatory Affairs Manager

Regulatory Affairs Manager

SimplyApplyOakland, CA, United States
Full-time
Plans, coordinates, monitors compliance with federal, state and local regulations; manages accreditation activities necessary for maintaining required accreditation. manages requirements for certif...Show moreLast updated: 1 day ago
  • Promoted
Associate Director Regulatory Affairs - APAC - Diabetes Care

Associate Director Regulatory Affairs - APAC - Diabetes Care

AbbottAlameda, CA, US
$144,100.00–$288,300.00 yearly
Full-time
Abbott is a global healthcare leader that helps people live more fully at all stages of life.Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses an...Show moreLast updated: 3 days ago
Regulatory Affairs Manager

Regulatory Affairs Manager

Alameda Health SystemOAKLAND, US
2 days ago
Job type
  • Full-time
Job description

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 organization’s 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 : Master’s 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 : Bachelor’s 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

Services As Needed / Per Diem

Varies

Business Professional & IT

FTE : 0.01