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

Regulatory Specialist

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 3 days ago
Similar jobs that could be interesting for youBased on the Regulatory Specialist in Irvine, CA vacancy
  •  ...Jenavalve Technology Inc in Irvine, CA, seeks a Senior Specialist in Regulatory Affairs to lead global regulatory activities. The role involves preparing regulatory submissions, overseeing reporting, and ensuring compliance with medical device regulations. The ideal candidate... 
    Suggested

    JenaValve Technology, Inc.

    Irvine, CA
    1 day ago
  •  ...Immediate hire for a Jr. Regulatory Affairs Specialist that will support product development teams to deliver regulatory inputs, strategies, reports and other design control deliverables. Prepare Quality Assurance/Regulatory reports and present status in review meetings... 
    Suggested
    Immediate start

    ConsultNet Technology Services and Solutions

    Irvine, CA
    2 days ago
  •  ...The Kardion Regulatory Affairs team is seeking a high energy, driven individual who is looking for the unique opportunity and challenge...  ...and team fit are paramount. The Principal Regulatory Affairs Specialist is a senior technical expert and strategic problem solver within... 
    Suggested
    Full time
    Contract work
    Remote work
    3 days per week

    Kardion

    Irvine, CA
    1 day ago
  •  ...Embla Medical, a part of Össur, seeks a Compliance Specialist to support the Director of Compliance in managing the Americas compliance program across state and federal regulations and company code of conduct. Responsibilities include auditing, monitoring, training coordination... 
    Suggested

    Össur

    Irvine, CA
    1 day ago
  •  ...Regulatory Affairs Specialist Responsibilities Regulatory Affairs is responsible for planning, coordinating and implementing regulatory submissions for products that require government approval. Demonstrates working knowledge of healthcare-related regulations. Demonstrates... 
    Suggested
    Contract work

    Indotronix Avani Group

    Irvine, CA
    4 days ago
  •  ...ConsultNet Technology Services and Solutions is hiring a Jr. Regulatory Affairs Specialist in Irvine, CA to support product development teams with regulatory inputs, strategies, and design controls. You will prepare QA/regulatory reports and present status in review meetings... 

    ConsultNet Technology Services and Solutions

    Irvine, CA
    1 day ago
  • Prismatik Dentalcraft is a division of Glidewell Dental. We are seeking an experienced Regulatory Affairs Specialist to support global regulatory compliance and drive high‑impact submissions. In this role, you’ll lead FDA 510(k)/PMA filings, maintain international registrations... 

    PRISMATIK DENTALCRAFT, INC.

    Irvine, CA
    3 days ago
  • $86k - $119.2k

    Bio-Rad is looking for a Regulatory Affairs Specialist II to join our Irvine, CA office. In this position you will support new product developments/product modifications, IVDR implementation, and international product registrations. This position must be based in Irvine... 
    Work at office

    Bio-Rad Laboratories

    Irvine, CA
    13 hours ago
  •  ...A reputable medical devices company is seeking a Senior Regulatory Affairs Coordinator for an onsite position in Irvine, CA. The role involves supporting US and EU regulatory submissions, developing regulatory strategies, and providing guidance on registration. Candidates... 
    Contract work
    Work at office

    MILLENNIUMSOFT

    Irvine, CA
    1 day ago
  •  ...Job Title: Senior Specialist, Regulatory Affairs Role Level: Individual Contributor Supervisor/Manager Title: Senior Manager, Regulatory Affairs Job Location & Environment: Irvine, CA – Corporate Office Environment Job Description Summary: Responsible for global regulatory... 
    Work at office

    JenaValve Technology, Inc.

    Irvine, CA
    1 day ago
  •  ...cardiovascular and interventional space. As the company continues to expand its global footprint, they are seeking a Senior Regulatory Affairs Specialist to support regulatory strategy, submissions, and global compliance activities across the product lifecycle. This is an... 

    EPM Scientific

    Irvine, CA
    5 hours ago
  • $63.44k - $96.72k

     ...Select how often (in days) to receive an alert: Sr. Regulatory Compliance Specialist Location: Irvine, CA, US, 92618 Position Summary: The Senior Regulatory Compliance Specialist is responsible for supporting the implementation of the strategic food regulatory and nutrition... 
    Work at office
    Local area

    VENTURA FOODS LLC

    Irvine, CA
    4 days ago
  •  ...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 the acceptability of documentation... 

    Katalyst CRO

    Irvine, CA
    3 days ago
  •  ...Jenavalve Technology is hiring a Senior Specialist for Regulatory Affairs in Irvine, CA with a strong focus on managing regulatory communication and submissions. The role requires substantial experience in medical device regulations, ensuring compliance with quality standards... 

    JenaValve Technology, Inc.

    Irvine, CA
    2 days ago
  •  ...Edwards Lifesciences is seeking a Regulatory Affairs professional in California to guide submissions for domestic and international devices. You will collaborate with manufacturing and development teams, prepare comprehensive regulatory packages, and monitor global regulatory... 

    Edwards Lifesciences

    Irvine, CA
    2 days ago
  •  ...A clinical stage startup in Irvine, CA is seeking a Principal Regulatory Affairs Specialist to lead the execution of key U.S. FDA submissions for Class III cardiovascular medical devices. The role involves developing regulatory strategies, partnering with cross-functional... 

    Kardion

    Irvine, CA
    1 day ago
  •  ...Job Summary The Regulatory Affairs Specialist (FDA, DEA) will ensure BaRupOn’s pharmacy, manufacturing, and healthcare operations meet all applicable regulatory requirements. This position is responsible for preparing submissions, maintaining licenses, coordinating audits... 

    BaRupOn LLC

    Irvine, CA
    1 day ago
  •  ...Glidewell Dental. Essential Functions Prepare and submit product registrations and submissions (510(k), PMA) to FDA and other regulatory bodies. Maintains company registrations and device listings in the US, Canada, and the EU. Analyzes and reports department metrics... 

    PRISMATIK DENTALCRAFT, INC.

    Irvine, CA
    1 day ago
  •  ...BCG Attorney Search in Newport Beach, CA, seeks a Technology Specialist to work within their Intellectual Property practice. The role involves drafting patent applications, corresponding with the patent office, and advising patent litigation teams, offering hands-on training... 
    Work at office
    Flexible hours

    BCG Attorney Search

    Newport Beach, CA
    1 day ago
  •  ...Job Title - Regulatory Affairs Consultant Job Location - 17200 Laguna Canyon Road, Irvine, California, United States of America, 92618 Contract Duration: 12 months and more (Hybrid , 2 days per week onsite) Job Description: We are seeking a highly detail-oriented and... 
    Full time
    Contract work
    2 days per week

    Stellar Consulting Solutions, LLC

    Irvine, CA
    2 days ago
  • $120k - $155k

     ...Lead regulatory strategy and submission activities for Qnovia's drug-device combination products across FDA, MHRA, and other global regulatory...  ...the United States and United Kingdom. As a Regulatory Affairs Specialist, you will develop and execute regulatory strategies, prepare... 
    Local area
    Flexible hours

    Qnovia, Inc.

    Newport Beach, CA
    4 days ago
  • $38.46 - $40.87 per hour

     ...THIS POSITION WILL BE LOCATED IN WILIMINGTON, CA 90744 Ensure compliance with LIHTC, HUD, and other owner, investor, lender, and regulatory agency requirements. Audit move‑in, recertification, and eligibility files; prepare and submit required compliance reports; track... 
    Hourly pay
    Full time
    Work at office
    Monday to Friday
    Flexible hours

    WSH MANAGEMENT INC

    Irvine, CA
    13 hours ago
  •  ...seeking a senior Research Compliance professional to oversee institutional research integrity, sponsored research accountability, and regulatory compliance activities. The role applies expert knowledge of federal, state, and university regulations related to research... 
    Remote work

    University-of-California,-Irvin

    Irvine, CA
    1 day ago
  •  ...leading technology firm in California is seeking a Trade Compliance Specialist responsible for the ECCN and HTS classification of technology...  ...U.S. Export Control Laws, the ability to navigate intricate regulatory standards, and proficient technical skills in analyzing... 

    Ingram Micro

    Irvine, CA
    4 days ago
  •  ...ByteLight is seeking a Senior Analyst, Trade Operations Americas to lead regulatory oversight of imports/exports across the U.S., Mexico, Canada and LATAM. The role reports to the Senior Manager, Global Trade Compliance Operations and requires close collaboration with... 

    ByteLight

    Costa Mesa, CA
    1 day ago
  • Safran Cabin in Costa Mesa, CA, is seeking an Expense Compliance Analyst to join the Finance team. You will review employee expense reports in Concur to ensure adherence to T&E policies and internal controls. This role supports policy improvements and assists with month...

    Safran S.A.

    Costa Mesa, CA
    1 day ago
  • $84k - $85k

     ...Compliance Specialist Avanath is proud to be named one of the top communities management companies to provide affordable housing for...  ...and attend affordable and LIHTC audits performed by state and regulatory agencies. Review applications and determine eligibility for... 
    Contract work
    Local area
    Immediate start
    Flexible hours

    Avanath Capital, LLC

    Irvine, CA
    13 hours ago
  • $99.4k - $124.3k

     ...are 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
    Local area

    Origence

    Irvine, CA
    1 day ago
  • At Volex, we are dedicated to improving the quality of life around the world by bringing connectivity and power to high tech equipment that is changing how we live, work, and communicate. We invest in developing our production sites to meet our customers’ evolving requirements...
    Internship
    Work at office
    Local area

    Volex

    Irvine, CA
    5 hours ago
  • $23 - $25 per hour

     ...updates to key stakeholders Develop and maintain compliance training programs for employees to ensure understanding and adherence to regulatory requirements Collaborate with internal teams to assess compliance risks and implement effective controls and mitigation... 
    Hourly pay
    Full time
    Fixed term contract
    Work at office
    Local area
    Monday to Friday
    Shift work

    Alleviate

    Irvine, CA
    8 days ago

Do you want to receive more vacancies?

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