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:- ...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
- ...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
- ...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...SuggestedImmediate start
- ...Regulatory Affairs Specialist 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, including...SuggestedWork at office
- ...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...Suggested
- ...Westcliff University is seeking a Regulatory Specialist to manage regulatory compliance, accreditation, licensure, and related reporting across the university and affiliated institutions. You will coordinate documentation, ensure timely submissions, and work with academic...
- ...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...Full timeContract workRemote work3 days per week
$92k - $138k
...and other neurovascular conditions. The team partners across regulatory, quality, engineering, clinical, and commercial functions to maintain... ...is expected to be minimal.The Senior Regulatory Affairs Specialist supports regulatory compliance and product lifecycle management...Full timeH1bWork at officeLocal areaImmediate startFlexible hours$85k - $130k
Job SummarySr Regulatory Affairs Specialist is an accomplished regulatory professional with a successful work history with leading regulatory initiatives and partnering with Sales and Marketing teams in obtaining domestic and internal regulatory clearances for Masimo products...Work experience placementLocal areaWorldwideFlexible hours- 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...
- 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...Contract work
- 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...
- ...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...
- ...Senior Regulatory Affairs Specialist Work mode: Hybrid Onsite Location(s): Marlborough, MA, US, 01752 Additional Location(s): US-CA-Irvine; US-MN-Arden Hills; US-MN-Maple Grove Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance...Work at officeLocal areaRelocation3 days per week
$95.8k - $159.6k
...Senior International Regulatory Affairs Specialist Irvine, CA Join a team focused on bringing medical technologies to market while ensuring compliance with global regulatory requirements. In this role, you will support regulatory strategy, submissions, and product lifecycle...Temporary workLocal areaFlexible hours- ...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
$63.44k - $96.72k
...Sr. Regulatory Compliance SpecialistLocation: Irvine, CA, US, 92618 Employment Type: Salaried Work Arrangement: Remote Position Summary: The Senior Regulatory Compliance Specialist is responsible for supporting the implementation of the strategic food regulatory and nutrition...Work at officeLocal areaRemote work- ...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...
- ...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...
- 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...
$110.1k - $183.4k
Irvine, CA In this International Regulatory Affairs role, you will ensure global product registrations move efficiently and compliantly through diverse regulatory pathways. This is a meaningful opportunity to drive operational excellence, collaborate across global teams...Temporary workLocal areaFlexible hours$90k - $140k
...Regulatory Strategy Lead 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 genomic and proteomic...- ...University of California, Irvine seeks a Regulatory Compliance professional to coordinate accreditation and licensing activities for UCI Health. The role includes reviewing controls, developing policies, and guiding staff on regulatory standards, partnering with regulatory...
$80k - $95k
...Regulatory Affairs SpecialistThe 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...Work at officeWorldwideWeekend workAfternoon shift$70k - $90k
...Compliance Specialist CopperPoint has an exciting opportunity for a Compliance Specialist. In this role, you'll help develop and administer an effective regulatory compliance program that ensures adherence to state regulatory and statutory requirements. You'll research...Hourly payTemporary workFlexible hours$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 payFull timeWork at officeMonday to FridayFlexible hours$99.4k - $124.3k
...Compliance Specialist (Regulatory Change & Governance)Shaping the Future of LendingWith 30 years of fintech leadership, Origence empowers credit unions with innovative SaaS lending solutions that make lending more accessible, efficient, and competitive. We invest in our...Full timeLocal area- ...Kura Sushi USA in Irvine, CA is seeking a GRC Senior Regulatory Compliance Analyst to join our hybrid team. You will assist the Integrated GRC Senior Manager to ensure Kura meets legal, regulatory and internal standards across operations, contracts and vendor engagements...
- ...Associate for its Irvine, CA office. The successful candidate will have 2 to 5 years of experience in transactional matters and regulatory compliance, with exposure to export controls, sanctions, and CFIUS considerations. The role emphasizes detailed regulatory analysis...Work at office
- 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...
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Regulatory Specialist. Be the first to apply!
- regulatory affairs specialist Irvine, CA
- medicare compliance specialist Irvine, CA
- senior compliance analyst Irvine, CA
- regulatory compliance analyst Irvine, CA
- compliance specialist Irvine, CA
- aml compliance analyst Irvine, CA
- regulatory officer Irvine, CA
- healthcare compliance officer Irvine, CA
- regulatory analyst Irvine, CA
- regulatory specialist Irvine, CA

