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
- 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...SuggestedWork at office
- ...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
$60 per hour
...Take your regulatory affairs expertise to the next level with an opportunity to support innovative diagnostic products on a global scale... ...:00 PM Why This Role Matters As a Regulatory Affairs Specialist III, you will help ensure critical diagnostic products meet...SuggestedHourly payTemporary workMonday to Friday- ...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...Suggested
$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- 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...
$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$76k - $121.9k
...dignity of our employees and recognize their merit. Job Function Regulatory Affairs Group Job Sub Function Regulatory Affairs Job Category... ...Johnson & Johnson is recruiting for a Regulatory Affairs Specialist II, MedTech Neurovascular. At Johnson & Johnson,we believe health...Temporary workLocal area- 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...
$60 per hour
Our client, a leading organization in the medical device and diagnostics industry, is seeking a Regulatory Affairs Specialist to join their team. As a Regulatory Affairs Specialist, you will be part of the Regulatory Affairs department supporting global product registration...Hourly payTemporary workMonday to FridayShift work- 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
$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 officeLocal area- 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
- ...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...
$89.2k
...quality of patient care with innovative Urology solutions. We are looking to hire an enthusiastic individual for a Senior Regulatory Affairs Specialist position (hybrid work mode) supporting our rapidly growing active implantable device portfolio. This role will be...Hourly payWork at officeLocal areaRelocationShift work3 days per week- ...Principal Regulatory Affairs Specialist Diality is a medical device company focused on developing solutions to improve lives impacted by kidney disease. Diality offers the Moda-flx Hemodialysis System, a user-friendly, mobile, and connected hemodialysis system designed...Work at officeRemote work
- 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...
$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 timeTemporary workImmediate startWorldwideFlexible hours$32 - $36 per hour
...Regulatory Affairs Associate Location: Tustin, CA Schedule: Monday–Friday, 9:00 AM–5:00 PM Pay: $32–$36 per hour, based on experience and qualifications Employment Type: Temporary-to-Hire A growing biotechnology company in Tustin is seeking a Regulatory Affairs...Hourly payTemporary workWork at officeMonday to Friday- ...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...
$68k - $75k
...Zymo Research is looking for a motivated individual to join our Regulatory Affairs team! In this role, you will play a vital part in supporting regulatory activities and maintaining compliance with applicable requirements, utilizing your skills and expertise in regulatory...H1bLocal areaWork visaFlexible hours$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...$80k - $95k
...Regulatory Affairs Specialist 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...Work at officeWorldwideWeekend workAfternoon shift$61.12k - $95.39k
...Supports solutions. Helping people live a Life Without Limitations is why we exist as a company. About the Role The Compliance Specialist is responsible for assisting the Director of Compliance in the management of the compliance program for Embla Medical's Americas...Full timeWork experience placementLocal area- ...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...Work at office
$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- ...a Compliance Analyst to support the BSA & Compliance Officer in implementing compliance programs. This role involves monitoring regulatory requirements, conducting compliance reviews, and assisting in risk assessments. The ideal candidate will have a degree in business...
$23 - $25 per hour
...work schedule. The ideal candidate will have at least 2 years of relevant experience, strong analytical skills, and a thorough understanding of regulatory requirements. Join a mission-driven team dedicated to providing innovative debt relief solutions! #J-18808-Ljbffr...Hourly payFull time$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 timeLocal area
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Regulatory Specialist. Be the first to apply!
- regulatory compliance analyst Irvine, CA
- medicare compliance specialist Irvine, CA
- regulatory analyst Irvine, CA
- senior compliance officer Irvine, CA
- legal compliance officer Irvine, CA
- senior compliance analyst Irvine, CA
- regulatory specialist Irvine, CA
- risk and compliance analyst Irvine, CA
- aml compliance analyst Irvine, CA
- regulatory compliance associate Irvine, CA

