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Regulatory Associate Jobs in Santa Rosa, CA (NOW HIRING)

Tax Associate

Sonoma, CA · On-site +1

$145K - $300K/yr

CFM is seeking Associates with experience advising private funds on formations, fundraising, and ... regulatory compliance or tax. * Tax LLM preferred We offer competitive salary, bonuses, 401(K) ...

Tax Associate

Santa Rosa, CA · On-site +1

$145K - $300K/yr

CFM is seeking Associates with experience advising private funds on formations, fundraising, and ... regulatory compliance or tax. * Tax LLM preferred We offer competitive salary, bonuses, 401(K) ...

Associate Informaticist

Saint Helena, CA · On-site

$32.79 - $44.98/hr

Associate's/Technical Degree in one of the following fields of study: patient care technician ... activities during regulatory surveys, operational projects, downtimes etc. to ensure care ...

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Regulatory Associate information

See Santa Rosa, CA salary details

$18

$35

$53

How much do regulatory associate jobs pay per hour?

As of May 28, 2026, the average hourly pay for regulatory associate in Santa Rosa, CA is $35.21, according to ZipRecruiter salary data. Most workers in this role earn between $26.83 and $41.78 per hour, depending on experience, location, and employer.

What Does a Regulatory Associate Do?

As a regulatory associate or regulatory affairs associate, your job is to coordinate compliance with internal—and occasionally external—regulations. This work involves checking each inspection review for accuracy, using safety data sheets (SDS), gathering and compiling documentation for products, and submitting material for license renewals and registrations. In this role, you often create management templates, study existing report documents, oversee the collection of consent forms, and audit the company for any sign of regulatory noncompliance. Some regulatory associates frequently travel to perform audits at various locations. Depending on the industry, you may have additional tasks that involve meeting state or federal guidelines.

What are the key skills and qualifications needed to thrive as a Regulatory Associate, and why are they important?

To thrive as a Regulatory Associate, you need strong attention to detail, knowledge of regulatory guidelines (such as FDA or EMA), and a relevant degree in life sciences or a related field. Familiarity with regulatory submission systems, document management tools, and electronic common technical document (eCTD) software is typically required. Excellent organizational skills, communication abilities, and the capacity to manage deadlines make candidates stand out. These skills ensure accurate regulatory submissions, compliance with evolving regulations, and effective collaboration across teams, all of which are crucial for product approvals and market access.

What are some common challenges Regulatory Associates face when working with cross-functional teams?

Regulatory Associates often work closely with teams from R&D, quality assurance, clinical, and legal departments to ensure compliance throughout product development and approval processes. A common challenge is navigating differing priorities and timelines among these groups, which requires strong communication and organizational skills. Additionally, Regulatory Associates must interpret and clarify complex regulatory requirements to various stakeholders, ensuring everyone is aligned and informed. Building collaborative relationships and proactively addressing potential misunderstandings are key to overcoming these challenges.

What is a Regulatory Associate?

A Regulatory Associate is a professional who supports regulatory affairs teams in ensuring that a company complies with all relevant laws and regulations, particularly in industries like pharmaceuticals, biotechnology, and medical devices. They assist in preparing, submitting, and maintaining regulatory filings and documentation required by government agencies. Regulatory Associates also help track changes in regulations and support product development by ensuring all necessary approvals are obtained for products to enter the market.

What is the difference between Regulatory Associate vs Compliance Specialist?

AspectRegulatory AssociateCompliance Specialist
Required CredentialsBachelor's degree in life sciences, regulatory affairs, or related field; certifications like RAC are a plusBachelor's degree in law, business, or related; certifications like CCEP may be relevant
Work EnvironmentPharmaceutical, biotech, or medical device companies; regulatory departmentsCorporate compliance departments across various industries, including healthcare and finance
Employer & Industry UsageUsed in regulated industries to prepare and submit regulatory documentsUsed to ensure company adherence to laws and regulations, often involving audits and policy development

The Regulatory Associate primarily focuses on preparing and managing regulatory submissions within life sciences industries, while the Compliance Specialist ensures ongoing adherence to laws and regulations across various sectors. Both roles require similar educational backgrounds and certifications, but their core responsibilities and work environments differ slightly, with Regulatory Associates working more directly with regulatory agencies and Compliance Specialists focusing on internal compliance processes.

What are the most commonly searched types of Regulatory jobs in Santa Rosa, CA? The most popular types of Regulatory jobs in Santa Rosa, CA are:
What job categories do people searching Regulatory Associate jobs in Santa Rosa, CA look for? The top searched job categories for Regulatory Associate jobs in Santa Rosa, CA are:
What cities near Santa Rosa, CA are hiring for Regulatory Associate jobs? Cities near Santa Rosa, CA with the most Regulatory Associate job openings:
Infographic showing various Regulatory Associate job openings in Santa Rosa, CA as of May 2026, with employment types broken down into 1% As Needed, 77% Full Time, 19% Part Time, and 3% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $73,245 per year, or $35.2 per hour.
Regulatory and Quality Specialist (St. Helena)

Regulatory and Quality Specialist (St. Helena)

Adventist Health

Saint Helena, CA • On-site

Full-time

This job post has expired today. Applications are no longer accepted.


Adventist Health rating

7.8

Company rating: 7.8 out of 10

Based on 237 frontline employees who took The Breakroom Quiz

101st of 864 rated healthcare providers


Job description

Quality And Regulatory Specialist

Located in the metropolitan area of Sacramento, the Adventist Health corporate headquarters have been based in Roseville, California, for more than 40 years. In 2019, we unveiled our WELL-certified campus - a rejuvenating place for associates systemwide to collaborate, innovate and connect. Adventist Health Roseville and shared service teams have access to enjoy a welcoming space designed to promote well-being and inspire your best work.

Plays a key role in supporting accreditation readiness, regulatory compliance, and quality improvement activities at the facility and network level. Reporting to the Manager of Quality and Regulatory Compliance, this role assists in implementing day-to-day processes that align with the standards of the Centers for Medicare and Medicaid Services (CMS), The Joint Commission (TJC), state agencies, and other regulatory and accrediting bodies. Responsible for performing tracers, audits, and monitoring activities that identify compliance gaps and improvement opportunities. Working closely with clinical and non-clinical staff, helps translate regulatory requirements into daily workflows, provides frontline coaching, and documents findings to ensure timely follow-up and closure of action items. Contributes to maintaining accurate regulatory documentation, survey files, and performance dashboards. Supports the preparation and logistics of external surveys and assists in compiling evidence, data, and reports that demonstrate compliance and quality outcomes. Collaborates with nursing, medical staff, and quality leaders and gathers and analyzes data related to patient safety, clinical effectiveness, and regulatory compliance. Helps track corrective action plans, supports quality improvement initiatives, and escalates risks or unresolved issues to the Manager for further action. Serves as a hands-on resource for departments, the Quality and Regulatory Specialist fosters a culture of continuous readiness, regulatory excellence, and high-quality care delivery across the organization.

Job Requirements:

Education and Work Experience:

  • Associate's/Technical Degree or equivalent combination of education/related experience: Required
  • Two years' experience in healthcare: Required
  • Three years' experience with health care compliance and regulatory activities and two years with project management experience: Preferred
  • Prior experience facilitating small-scale project teams or improvement initiatives: Preferred
  • Exposure to Lean, Six Sigma, or other improvement methodologies: Preferred

Licenses/Certifications:

  • Lean or Six Sigma Green Belt or GE Change Management certification: Required within two years of hire
  • Lean or Six Sigma Green Belt (LGB) or PROSCI-CCMP: Required

Essential Functions:

  • Maintains and controls all regulatory, licensure and accreditation documents. Monitors Joint Commission standards compliance. Conducts periodic internal reviews and/or audits to ensure compliance procedures are followed. Identifies compliance issues that require follow-up or investigation.
  • Coordinates logistics for regulatory and accrediting body surveys, including scheduling communications, team assignments, and preparation of materials for surveyors and internal stakeholders. Supports the evaluation, planning and continuous readiness activities to maintain deemed status accreditation (e.g. The Joint Commission) and compliance with federal, state, and local regulatory requirements and licenses.
  • Administers and supports use of tracer management systems including development of tracers/audits, user assignments, report generation, training and oversight to ensure adherence to systemwide requirements. Supports design and execution of performance improvement initiatives under the guidance of program managers or senior leaders. Assists with project planning, team coordination, charter development, and progress tracking to ensure deliverables are achieved.
  • Facilitates small-scale quality and performance improvement projects aimed at enhancing clinical outcomes, efficiency, and patient experience. Applies basic Lean, Six Sigma, PDSA, or other improvement methodologies to identify process gaps and implement corrective actions. Collects, validates, and analyzes quality, operational, and performance data. Prepares and presents reports, dashboards, and scorecards to leaders, committees, and frontline teams to identify trends, variation, and opportunities for improvement.
  • Provides basic coaching and support to staff and leaders on improvement tools, methods, and techniques. Collaborates with interdisciplinary teams to share best practices and support adoption of standardized workflows. Monitors improvement project outcomes and assists with follow-up actions to ensure sustainability of changes. Documents lessons learned and promotes organizational learning to support continuous performance improvement.
  • Performs other job-related duties as assigned.

Organizational Requirements:

Adventist Health is committed to the safety and wellbeing of our associates and patients. Therefore, we require that all associates receive all required vaccinations as a condition of employment and annually thereafter, where applicable. Medical and religious exemptions may apply. Adventist Health participates in E-Verify. Visit https://adventisthealth.org/careers/everify/ for more information about E-Verify. By choosing to apply, you acknowledge that you have accessed and read the E-Verify Participation and Right to Work notices and understand the contents therein.

About Us

Adventist Health is a faith-based, nonprofit, integrated health system serving more than 100 communities on the West Coast and Hawaii with over 440 sites of care, including 27 acute care facilities. Founded on Adventist heritage and values, Adventist Health provides care in hospitals, clinics, home care, and hospice agencies in both rural and urban communities. Our compassionate and talented team of more than 38,000 includes employees, physicians, Medical Staff, and volunteers driven in pursuit of one mission: living God's love by inspiring health, wholeness and hope.

Job Info

  • Job Identification 63141
  • Job Category Specialist
  • Posting Date 05/13/2026, 06:48 PM
  • Locations 10 Woodland Road, Saint Helena, CA, 94574, US
  • Job Shift Day Shift
  • Assignment Category Full-time regular
  • Pay Range The estimated base pay for this position is $81,273 to $121,909. Additional individual compensation may be available for this role through differentials, extra shift incentives, bonuses, etc. Base pay is only a portion of the total rewards package, and a comprehensive benefits program is available for qualifying positions. Please contact our Talent Acquisition team for more information.
  • Hiring Department Quality Resources
  • Shift Length 8 Hours

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