Sign up to access all features of our service.
  • Job search
  • Favorites
  • Create a CV
    New
  • Salaries
  • Subscriptions

Regulatory Specialist

Full-time

Westcliff University

Job Description

Job Description

Description:

What if I told you it is possible to find a Company that lived to educate, inspire and empower others while creating a family atmosphere that truly appreciates and respects their team? Would you apply? What if I threw in strong Company values, outstanding benefits, and the opportunity for you to make a tangible impact and feel appreciated?

See below for a feel of what the Company culture is (REALLY) like. Hint: it's amazing.

At Westcliff, we are constantly striving to be the best while valuing each of our team members as human beings and succeeding together!

Westcliff is a leader in innovative global education. We are respected for our transformative, technologically advanced programs and initiatives with a focus on excellence, social responsibility, and diversity. Our tagline – “Educate. Inspire, Empower.” – is a summary of our Mission Statement. As it suggests, the main focus of our University is to strive to enhance the opportunities of our students and employees to enjoy success through empowerment, as a result of their education and hard work.

By joining the Westcliff team, you’ll be playing a significant role in our growth, having an opportunity to put your personal touch on Westcliff’s progress as we grow and succeed together!

Regulatory Specialist

JOB SUMMARY

The Regulatory Specialist supports regulatory compliance, accreditation, authorization, and licensure activities for Westcliff University and its related institutions. This position assists in securing approvals and maintaining compliance with institutional accreditation, state and provincial regulatory bodies, licensing boards, and other governing agencies. The Regulatory Specialist coordinates documentation, reporting, monitoring, and compliance-related processes to support ongoing regulatory pursuits, obligations, and readiness. Working collaboratively with academic and administrative departments and reporting to the Director of Regulatory Initiatives, the position helps ensure the university secures the necessary approvals for its initiatives, maintains compliance, supports continuous quality improvement initiatives, and remains prepared for reviews, audits, site visits, and regulatory reporting requirements. 

 

Duties and Responsibilities

  • Support the university’s compliance with institutional accreditation standards, state and provincial regulations, licensing boards, and other regulatory requirements.
  • Coordinate the preparation, submission, and maintenance of accreditation, authorization, licensure, and regulatory reports, applications, renewals, and related documentation.
  • Monitor regulatory and accreditation requirements, deadlines, substantive changes, and reporting obligations to ensure ongoing compliance.
  • Collect, organize, validate, and maintain compliance and accreditation records, evidence, and supporting documentation.
  • Assist with accreditation reviews, self-studies, site visits, audits, annual reports, and continuous quality improvement initiatives.
  • Research and communicate changes in regulatory, accreditation, and licensure requirements and assess potential impacts on university operations.
  • Collaborate with academic and administrative departments to gather data, coordinate compliance activities, and support regulatory and accreditation initiatives.
  • Track compliance findings, recommendations, corrective actions, and improvement plans to support accreditation readiness and institutional effectiveness.
  • Prepare reports, summaries, presentations, and other materials for university leadership, accrediting agencies, and regulatory bodies.
  • Maintain compliance calendars, tracking systems, and documentation repositories to support timely and accurate reporting.
  • Assist with policy and procedure reviews to ensure alignment with applicable regulatory and accreditation requirements.
  • Perform other related duties as assigned.

Qualifications

  • Bachelor’s degree required (education, healthcare administration, or related field preferred); Master’s degree preferred.
  • 2–5 years of experience in higher education compliance, accreditation, institutional effectiveness, regulatory affairs, or a related field.
  • Knowledge of higher education accreditation standards and regulatory frameworks required. Direct experience with Westcliff’s accreditors and regulatory bodies preferred.
  • Strong project management, organizational, and documentation skills.
  • Experience coordinating complex projects involving multiple stakeholders and deadlines.
  • Proficiency with Microsoft Office Suite, data management systems, and document repositories.
  • Excellent written, verbal, analytical, and interpersonal communication skills.
  • Ability to manage multiple priorities while maintaining a high level of accuracy and attention to detail.

 

Limitations and Disclaimer

The above job description is meant to describe the general nature and level of work being performed; it is not intended to be construed as an exhaustive list of all responsibilities, duties and skills required for the position. All job requirements are subject to possible modification to reasonably accommodate individuals with disabilities. Some requirements may exclude individuals who pose a direct threat or significant risk to the health and safety of themselves or other employees. This job description in no way states or implies that these are the only duties to be performed by the employee occupying this position. Employees will be required to follow any other job-related instructions and to perform other job-related duties requested by their supervisor in compliance with Federal and State Laws. Requirements are representative of minimum levels of knowledge, skills and/or abilities. To perform this job successfully, the employee must possess the abilities or aptitudes to perform each duty proficiently. Continued employment remains on an at-will basis, unless otherwise contractually bound.

Westcliff University is an Equal Opportunity Employer

Requirements:

Vacancy posted 2 days ago
Similar jobs that could be interesting for youBased on the Regulatory Specialist in Irvine, CA vacancy
  •  ...Manufacturing, and/or Project Management within the IVD industry. Knowledge of FDA, and CE marking requirements for IVD products is preferred. Excellent verbal and written communication skills. Thorough knowledge of policies, practices and procedures related to Regulatory Affairs.
    Suggested

    Katalyst Healthcares & Life Sciences

    Irvine, CA
    2 days ago
  • Job-ID31554631Reference25-04530 Responsibilities: This position is responsible for the preparation of regulatory submissions required to market medical devices in both the U.S. and Europe, support of international product registrations and related regulatory affairs activities... 
    Suggested
    Work at office

    Katalyst Healthcares & Life Sciences

    Irvine, CA
    2 hours ago
  • $55 - $60 per hour

     ...Take your regulatory affairs expertise to the next level with an opportunity to support innovative diagnostic products on a global scale...  ...-5:00 PM Why This Role Matters As a Regulatory Affairs Specialist III, you will help ensure critical diagnostic products meet global... 
    Suggested
    Hourly pay
    Temporary work
    Monday to Friday

    Manpower Group Inc.

    Irvine, CA
    1 day ago
  • $80k - $100k

     ...an impact in the lives of others. Learn about the Danaher Business System ( which makes everything possible. The Regulatory Affairs Specialist is responsible for obtaining domestic and internal regulatory clearances for Masimo products to meet business objectives... 
    Suggested
    Work experience placement
    Worldwide

    Danaher Corporation

    Irvine, CA
    3 days ago
  • $80k - $100k

     ...impact in the lives of others. Learn about the Danaher Business System which makes everything possible. The Regulatory Affairs Specialist is responsible for obtaining domestic and internal regulatory clearances for Masimo products to meet business objectives... 
    Suggested
    Full time
    Work experience placement
    Worldwide

    Danaher

    Irvine, CA
    14 days ago
  • Job-ID31853494Reference26-00237 Responsibilities: Represent Regulatory Affairs on cross-functional project teams and provide strategic input and technical guidance on product lifecycle planning and regulatory requirements for non-medical devices, and medical devices. Assess... 

    Katalyst Healthcares & Life Sciences

    Irvine, CA
    2 days ago
  • $80k - $100k

     ...Regulatory Affairs Specialist at Masimo, a Danaher medical technology company, manages domestic and international regulatory clearances for medical devices. The role involves preparing submissions, coordinating with regional teams, and ensuring compliance with regulatory... 
    Worldwide

    Danaher

    Irvine, CA
    14 days ago
  • $74k - $104k

     ...Edwards Lifesciences seeks a Regulatory Affairs Specialist to support corporate regulatory compliance and process improvements across global operations. The role involves analyzing regulatory changes, managing device listings and registrations, and collaborating with cross... 
    Work at office
    Worldwide

    Edwards Lifesciences

    Irvine, CA
    1 day ago
  • $110.1k - $183.4k

    Work Flexibility: Hybrid or OnsiteStaff International Regulatory Affairs SpecialistIrvine, CAIn this International Regulatory Affairs role, you will ensure global product registrations move efficiently and compliantly through diverse regulatory pathways. This is a meaningful... 
    Full time
    For contractors
    Local area

    Stryker

    Irvine, CA
    3 days ago
  • $127k - $153k

     ...to provide a broad range of prescriptions and meet the needs of any professional dialysis care setting. The Principal Regulatory Affairs Specialist will serve as a key contributor responsible for authoring and compiling regulatory submissions, providing regulatory... 
    Work at office

    Diality

    Irvine, CA
    1 day ago
  • Company DescriptionAt the dawn of the new millennium, a unique information technology company was born: HCL Technologies. As narrated in the video below, HCL Technologies has demonstrated remarkable growth through the recent economic downturn, emerging as one of only eight...

    Artech

    Irvine, CA
    2 days ago
  • $92.45k - $114.2k

     ...management, and other risk mitigation activities. You'll collaborate with all lines of defense departments to support adherence to regulatory commitments and the development of enhanced monitoring and controls to mitigate compliance risk.Interpret and effectively... 
    Full time

    Western Alliance Bancorporation

    Irvine, CA
    3 days ago
  • $85.8k - $137.3k

     ...supportPrepare on demand reports and SKU lists for Compliance Specialists and ManagementReview and upload approved classification data...  ...determined by SupervisorAdministrative support for required regulatory reporting requirements in a timely manner.Export Control Laws... 
    Full time
    Temporary work
    Immediate start
    Worldwide
    Flexible hours

    Ingram Micro

    Irvine, CA
    1 day ago
  • $90k - $140k

     ...Regulatory Strategy Lead For AI/ML-Based SaMD Product Execute on regulatory strategy of De Novo submissions for AI/ML-based Software as a Medical Device (SaMD) product, including AidaBreast. Serve as regulatory lead for novel oncology diagnostic technologies integrating... 

    PreludeDx

    Laguna Hills, CA
    1 day ago
  • $80k - $95k

     ...Job Purpose The Regulatory Affairs Specialist is responsible for coordinating and executing routine regulatory activities that support the company's worldwide medical device business. This position supports product registrations, regulatory submissions, approvals,... 
    Work at office
    Worldwide
    Weekend work
    Afternoon shift

    Nihon Kohden Orange Med

    Santa Ana, CA
    2 days ago
  • $40 - $46 per hour

     ...Job Description Job Description Trade Compliance Specialist This is an exciting opportunity to join a Global, industry leading company as a Trade Compliance Specialist. Responsibilities: Generate SAP reports to present KPIs in Tier 4 meetings and OTIF calls... 
    Hourly pay
    Full time

    Cypress HCM

    Irvine, CA
    2 days ago
  •  ...assist in the implementation and maintenance of the bank's compliance program. You will be responsible for monitoring and analyzing regulatory requirements, internal policies, and industry standards to ensure the bank operates in adherence to applicable laws and... 
    Full time
    Work at office

    CommerceWest Bank

    Irvine, CA
    2 days ago
  • Job Description Job Description The Compliance Coordinator is responsible for the accurate creation, tracking, and submission of fire life safety inspections, repairs, and retest reports. This role ensures all required documentation is complete, compliant, and delivered...
    Hourly pay
    Full time
    Weekend work

    Commercial Fire Protection, Inc.

    Irvine, CA
    2 days ago
  •  ...let’s grow and succeed together!   Records Compliance Specialist Job Summary: The Records Compliance Specialist at...  ...organizations, such as BPPE and WSCUC, by staying abreast of regulatory changes and compliance requirements. Collaborate with relevant... 
    Work at office
    Flexible hours

    Westcliff University

    Irvine, CA
    a month ago
  • $24 - $43 per hour

     ...Maintains proficient knowledge of applicable compliance statutes, regulations and interpretations. Provide assistance during regulatory examinations and independent audits at the direction of the Compliance Officer, including gathering of documentation and information... 
    Hourly pay
    Full time
    Work at office
    Local area
    Flexible hours

    Commercial Bank of California

    Irvine, CA
    5 days ago
  •  ...1% Better Each Day Join Our Team We are seeking a detail-oriented and highly organized Compliance Coordinator to support regulatory compliance activities across our Substance Use Disorder (SUD) treatment programs in Rhode Island. This position plays an important... 
    Work at office
    Remote work

    Zinnia Health LLC

    Irvine, CA
    4 days ago
  • Anduril Industries is seeking a People Compliance Coordinator in Costa Mesa, California. You will be responsible for coordinating background check processes and ensuring adherence to compliance regulations. The role requires 3+ years of experience in compliance or HR, alongside...

    Anduril

    Costa Mesa, CA
    6 days ago
  •  ...supporting Anduril's compliance initiatives. Your collaboration with cross-functional teams will be essential to ensure adherence to regulatory requirements, including background checks, I-9/right-to-work processes, mandatory employee trainings, and reporting obligations.... 
    Full time
    Work experience placement
    Local area
    Relocation
    Relocation package

    Anduril

    Costa Mesa, CA
    5 days ago
  •  ...The Associate Director Regulatory Affairs US Advertising and Promotion-Oncology  is responsible for setting strategy and leading cross-functional multidisciplinary therapeutic teams and executes multidivisional initiatives. The Associate Director envisions the future... 
    Full time
    Work at office
    Local area
    Remote work

    AbbVie

    Irvine, CA
    17 days ago
  •  ...month contract with possible extension QUALITY COMPLIANCE SPECIALIST Seeking a detail-oriented Quality Compliance Specialist...  ..., manufacturing, and post-market processes strictly adhere to regulatory frameworks like FDA 21 CFR Part 820, ISO 13485:2016, and EU MDR... 
    Hourly pay
    Contract work
    Local area

    Ledgent Tech

    Irvine, CA
    2 days ago
  • $74.5k - $99.5k

    Data Analyst Call Center Please Note: This position has a hybrid schedule which is 3 days onsite and 2 days remote. This role supports the ERS Call Center Analytics team by providing analytical and organizational assistance in developing and delivering accurate...
    Full time
    Local area
    Remote work

    AAA

    Costa Mesa, CA
    2 days ago
  • $146k - $194k

     ...military in months, not years.This position is looking for a highly motivated Program Manager with emphasis in FAA, DoD, and other regulatory organizations focused on FAA compliance and airspace access. Work closely with the program leadership, legal and a wide spectrum... 
    Full time
    Work experience placement
    Immediate start
    Remote work

    Anduril Industries

    Costa Mesa, CA
    4 days ago
  • $70k - $80k

     ...United States. We are looking for an experienced HR Compliance Specialist to join our Corporate HR team in Irvine California. Reporting...  ...will monitor employment requirements analyze HR data prepare regulatory reports and help translate legal and policy requirements into... 
    Full time
    For contractors
    Local area

    Global 1st Flagship

    Irvine, CA
    2 days ago
  • $99.4k - $124.3k

     ...excited by emerging technologies and eager to use them responsibly to solve problems and drive impact. The Compliance Specialist (Regulatory Change & Governance) is responsible for coordinating and executing compliance initiatives across Origence and its affiliated... 
    Full time
    Work at office
    Local area
    Flexible hours
    3 days per week

    Origence

    Irvine, CA
    19 days ago
  • $92k - $130k

     ...Senior Specialist in International Regulatory Affairs supporting the Transcatheter Mitral and Tricuspid Therapies business unit. Develop and track complex regulatory submissions for overseas markets, represent regulatory requirements to product development teams, and... 
    Overseas

    Edwards Lifesciences

    Irvine, CA
    14 days ago

Do you want to receive more vacancies?

Subscribe and receive similar vacancies to Regulatory Specialist. Be the first to apply!