Director, Regulatory Affairs
City Of Hope Hospital Duarte - Comprehensive Cancer Center
Regulatory and Accreditation Specialist – Performance Improvement Job Summary The Regulatory and Accreditation team member leads the strategic development, coordination, and execution of regulatory compliance and accreditation activities across the organization. This role ensures City of Hope meets or exceeds requirements set forth by federal and state regulatory bodies, national accrediting organizations, and internal policies to support compliance and deliver high‑quality patient care. This position supports performance and quality improvement initiatives by defining project scope, developing and monitoring timelines, and documenting outcomes to meet accreditation, regulatory, and quality standards. Responsibilities Manage small‑scale projects from concept through implementation. Assist in developing communication materials related to quality and regulatory initiatives (e.g., memos, newsletters, SharePoint or intranet content). Participate in larger, more complex projects as needed. Prepare internal and external reports by gathering, analyzing, and summarizing data for leadership and stakeholders. Manage and archive all quality‑related project documentation. Partner closely with clinical, administrative, legal, and quality teams to interpret evolving regulations, support survey and inspection readiness, and drive continuous improvement in compliance systems. Support enterprise‑wide initiatives and collaborate with leadership, departments, clinics, physicians, and administrative teams to promote regulatory excellence. Provide cross‑coverage within the Quality team as required. Position Qualifications Minimum Education: Degree in Healthcare Administration, Healthcare, Public Health, Compliance, or Nursing required. Minimum Experience: Minimum of three (3) years of experience in clinical nursing and/or quality, risk, or regulatory functions. Preferred Qualifications: Bachelor of Science in Nursing (BSN). Certification: Healthcare Accreditation Certification Program (HACP). Experience: Thorough knowledge of Joint Commission standards, Illinois Department of Public Health (IDPH), CMS Conditions of Participation, and other regulatory agencies. Skills & Abilities: Demonstrates sensitivity to patient care and patient privacy; strong interpersonal skills that promote trust and collaboration; professional demeanor fostering a positive organizational image; cultural sensitivity and awareness of diversity and inclusion; excellent verbal, written, organizational, and presentation skills; proficiency with computer applications and software tools; data analysis and data visualization skills; ability to build engagement and enthusiasm for quality and compliance initiatives. City of Hope is an equal opportunity employer. #J-18808-Ljbffr
$165k - $185k
...within the United States SUMMARY: The Senior Manager, Regulatory Strategy (US RA): supports the creation and implementation of... ...reviews and represents US regulatory perspective at Regulatory Affairs Focus Team (RAFT) meetings. Identifies risk, problem-solves,...SuggestedWork at officeRemote workFlexible hours$78k - $156k
...expert to assure successful investigations and corrective actions. Serves as a source of information on the IT Compliance needs and regulatory environment.What You’ll Work OnLeads the IT Compliance activities for specific CAPA (Corrective and Preventive Action) event...SuggestedWorldwide- What Regulatory Affairs contributes to Cardinal HealthRegulatory provides regulatory affairs and product development consulting services to enable pharmaceutical, medical and biotechnology companies to obtain regulatory approvals. This function applies subject matter expertise...SuggestedFull timeTemporary workWork experience placementWork at officeLocal areaImmediate start
- ...distributor of shipping, industrial and packaging materials! As a Senior International Trade Compliance Specialist, you’ll tackle regulatory hurdles, find tariff savings and bring Uline’s high quality products to international destinations.Careers Packed with Potential....SuggestedFull time
- ...please visit us at . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description The Director, Regulatory Affairs Data Standards and Governance is responsible for driving awareness and implementation of data standards and associated...SuggestedFull timeWork at officeLocal area
$123k - $205.1k
...execution without unnecessary delay. You will report to the Senior Director, Global Trade Compliance.This position is based in Lake Forest... ..., and controls tailored to the company's risk profile and regulatory requirements. Function as a hands-on operational leader for...Full timeWork at officeLocal areaWorldwide3 days per week- ...Manages the Regulatory Operations team responsible for various operational regulatory activities. Oversee the preparation, review and... ...or regulated industry, specifically three years in Regulatory Affairs Minimum of two years’ management experience Experience with Regulatory...
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- Connecting to a Career That Makes a Difference By submitting your application and selecting "Accept All", you confirm that you have read and understand this privacy statement and consent to the collection, use, and sharing of your personal information as described. Privacy...
- ...job opening with US Tech Solutions that fits your expertise and skillset. Job Description Serve as the senior and principal regulatory affairs member of project development teams, primarily focused on (but not limited to) drug products. Provide regulatory oversight and...
- • Develops regulatory strategies for development projects, design changes and manufacturing improvements, and analyzes risk vs. benefit... ...industry experience with a minimum of five years in regulatory affairs with direct experience and authoring 510(k) and/or CE...
- ...visit us at . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description The Senior Director, Global Regulatory Strategy Lead and FDA Regulatory SME is responsible for oversight of complex product development within and across...Full timeLocal areaImmediate start
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$110k - $150k
Astronics SubsidiaryAstronics CSC LocationWaukegan, IL DescriptionAstronics Connectivity Systems and Certification (formerly Telefonix PDT and Astronics Armstrong Aerospace) serves as the experienced, global market leader for in-flight entertainment and connectivity (IFEC...Full timeTemporary workPart timeFlexible hours$55.64k - $92.73k
...Functions: Ensures compliance with all state and federal regulatory requirements including, but not limited to, Anti-Money... ...Savings, Truth in Lending, Illinois Credit Union Act Advises Director of Risk and Senior Management of emerging compliance issues and...Local area- Job-ID29031369Reference26-22116Purpose: Describe the primary goals, objectives or functions or outputs of this position. Assure compliance with FDA current Good manufacturing Practices (cGMP) and Good Distribution Practices (cGDP) regulations. Assure compliance with Corporate...
- ...Responsible for the development and implementation of US and Canada regulatory strategic and tactical planning (RSTP) for assigned on market... ...communication on Regulatory/FDA issues including Public Affairs, Clinical Development, Legal, and others such as Commercial....Local area
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- ...Enhance Rehabilitation is now hiring a Director of Rehab to oversee rehabilitation services in one or more of our service locations!... ...ensure adherence to evidence-based care delivery standards and regulatory compliance Ensures the clinical management of the rehab department...Full timeContract workImmediate start
- ...efficiencies. Act as a trusted source for trade compliance insights by proactively tracking, interpreting, and communicating regulatory and legislative updates to GTC stakeholders—ensuring the organization stays ahead of potential impacts with timely and actionable...Full timeTemporary workLocal areaWorldwide
- Senior Pharmaceutical Recruiter - Unicon Pharma Inc Regulatory Affairs Specialist Provide regulatory support for U.S. and global medical device submissions, including FDA and EU requirements. Prepare and organize registration packages and maintain global regulatory dossiers...Contract work
- Responsibilities Provides regulatory advice and support to assigned products/teams. Identifies and communicates registration needs and... ...ease of regulatory agency review. Represents Global Regulatory Affairs at research and development meetings and presents agreed upon...Local area
$97.5k - $139.75k
Position Summary Provides regulatory support and expertise associated with global and US registration of medical device products, including... ...of regulatory agency review. Represents Global Regulatory Affairs at research and development meetings and presents agreed upon...Work at officeLocal area$68k - $136k
...medical devices, nutritionals and branded generic medicines. Our 115,000 colleagues serve people in more than 160 countries. Regulatory Affairs Specialist II Working at Abbott At Abbott, you can do work that matters, grow, and learn, care for yourself and your family,...Work experience placementWorldwide- Responsibilities Support regional Regulatory Information Management (RIM) activities using systems such as COSMOS, HUBBLE, and CIU. Create... ...initiatives. Requirements Bachelor's degree in Regulatory Affairs, Pharmacy, Health Sciences, or a related discipline. Experience...
$124.2k - $207k
...As the Sr. Manager, Federal Strategy, you will report to the Director, Market Strategy and lead the Government Federal Sales Segment... ...translating federal agency mission priorities, procurement behaviors, regulatory requirements, and contract vehicles into compelling bundled...Full timeContract workLive inLocal areaWorldwide$16.5 - $19 per hour
Quality Assurance Associate Waukegan, IL 60085 Overview Salary Range $16.50 - $19.00 Hourly Job Shift 3rd Shift Education Level High School/GED Category Quality Description Join the PAK The Visual Pak Companies are aligned with many of the largest consumer...Hourly payContract workWork experience placementWork at officeLocal areaFlexible hoursShift workNight shift- Quality Assurance Specialist Ready to proactively identify problems with products and goods? In manufacturing and industrial environments, that's what quality assurance specialists and technicians do best. If you have what it takes to report and verify defects, troubleshoot...Immediate start
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