1

Regulatory Program Manager Jobs in Riverside, CA

The Sr Technical Program Manager is responsible for driving Project Management Office (PMO) ... Quality, Regulatory, Operations, Clinical, and Product Management. Please note this is an onsite ...

The Sr Technical Program Manager is responsible for driving Project Management Office (PMO) ... Quality, Regulatory, Operations, Clinical, and Product Management. Please note this is an onsite ...

S. Food and Drug Administration started regulating such products in 1976. We are shaping the ... Program/project management experience preferred PMP and CAPM certification preferred. Working ...

Showing results 41-60

Regulatory Program Manager information

See Riverside, CA salary details

$40.2K

$112.1K

$163.8K

How much do regulatory program manager jobs pay per year?

As of Aug 8, 2026, the average yearly pay for regulatory program manager in Riverside, CA is $112,110.00, according to ZipRecruiter salary data. Most workers in this role earn between $82,900.00 and $138,200.00 per year, depending on experience, location, and employer.

What are some common challenges faced by regulatory program managers, and how can they be addressed in day-to-day work?

Regulatory Program Managers often encounter challenges such as navigating evolving regulatory requirements, coordinating across multiple departments, and ensuring timely submissions to regulatory bodies. Staying updated on changes in regulations and fostering strong communication with cross-functional teams are key to overcoming these hurdles. Leveraging project management tools and establishing clear processes can also help maintain compliance and keep projects on track. Building relationships with regulatory agencies and internal stakeholders further facilitates smoother approvals and minimizes delays.

What is the difference between Regulatory Program Manager vs Regulatory Affairs Specialist?

AspectRegulatory Program ManagerRegulatory Affairs Specialist
Required CredentialsBachelor's degree, certifications like RAC often preferredBachelor's degree, certifications like RAC often preferred
Work EnvironmentOversees multiple projects, manages teams, strategic planningFocuses on specific regulatory submissions, documentation, compliance
Employer & Industry UsageUsed in healthcare, pharmaceuticals, medical devicesCommon in similar industries, often collaborates with managers
Search & Comparison IntentUnderstanding managerial roles, project scopeDetailing compliance tasks, submission processes

The Regulatory Program Manager typically oversees multiple regulatory projects, manages teams, and develops strategic compliance plans. In contrast, the Regulatory Affairs Specialist focuses on preparing documentation, ensuring regulatory compliance for specific products, and supporting submissions. Both roles require similar credentials and are vital in regulated industries like healthcare and pharmaceuticals, but they differ in scope and responsibilities.

What are the key skills and qualifications needed to thrive as a regulatory program manager?

To excel as a Regulatory Program Manager, you need expertise in regulatory compliance, project management, and industry-specific regulations, often supported by a relevant degree and certifications like PMP or RAC. Familiarity with regulatory submission systems, document management tools, and compliance tracking software is typically required. Strong organizational skills, attention to detail, and effective communication are crucial soft skills for managing complex projects and diverse stakeholders. These abilities ensure regulatory objectives are met efficiently, reducing risks and supporting organizational success in a highly regulated environment.

What does a regulatory program manager do?

A Regulatory Program Manager oversees and coordinates regulatory compliance activities within an organization, often in industries such as pharmaceuticals, healthcare, finance, or energy. They ensure that the company meets all applicable laws, regulations, and industry standards by managing projects related to regulatory submissions, audits, and communications with regulatory agencies. Their role often includes developing strategies for regulatory approvals, monitoring changes in regulations, and working cross-functionally with other departments to maintain compliance. Effective Regulatory Program Managers help minimize compliance risks and support the organization's business objectives.
What job categories do people searching Regulatory Program Manager jobs in Riverside, CA look for? The top searched job categories for Regulatory Program Manager jobs in Riverside, CA are:
What cities near Riverside, CA are hiring for Regulatory Program Manager jobs? Cities near Riverside, CA with the most Regulatory Program Manager job openings:
Infographic showing various Regulatory Program Manager job openings in Riverside, CA as of August 2026, with employment types broken down into 1% As Needed, 75% Full Time, 19% Part Time, 1% Temporary, and 4% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $112,110 per year, or $53.9 per hour.

Sr Technical Program Manager

Masimo

Irvine, CA • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 12 days ago


Job description

Job Summary:

The Sr Technical Program Manager is responsible for driving Project Management Office (PMO) operational excellence through the development, standardization, implementation, and continuous improvement of project management processes, governance methodologies, portfolio management practices, reporting frameworks, and supporting technologies.

This role serves as a strategic partner to Project Management leadership and Engineering stakeholders, improving portfolio visibility, governance, resource planning, reporting, and organizational maturity across the engineering portfolio. The position leads PMO process improvement initiatives, develops executive portfolio reporting and performance metrics, supports portfolio governance and capacity planning, and enables data-driven decision making across Engineering, Software, Quality, Regulatory, Operations, Clinical, and Product Management.

Please note this is an onsite position at our Irvine, CA office. 

Duties & Responsibilities:

  • Drive PMO operational excellence through the development, implementation, standardization, and continuous improvement of project management methodologies, governance processes, tools, and execution frameworks. 
  • Partner with the Vice President of Project Management to translate Engineering portfolio strategy into scalable PMO processes, portfolio governance, analytics, and execution practices. 
  • Lead portfolio governance, project intake, prioritization, capacity planning, resource forecasting, and cross-project portfolio reviews to support strategic planning and investment decisions. 
  • Develop and maintain portfolio management frameworks, governance standards, operating procedures, templates, and best practices that improve execution consistency and organizational maturity across Engineering. 
  • Develop executive dashboards, portfolio reports, KPIs, portfolio health metrics, forecasting models, and performance analytics using Power BI and related reporting tools to enable data-driven decision making. 
  • Analyze portfolio performance, identify risks, trends, resource constraints, and dependencies, and provide actionable recommendations to Engineering leadership. 
  • Facilitate executive portfolio reviews by preparing portfolio summaries, decision-support materials, and recommendations while improving portfolio visibility, execution predictability, and delivery performance. 
  • Own the governance, optimization, and adoption of PMO collaboration and portfolio management tools, including Jira, Confluence, Power BI, and related platforms, ensuring data integrity and reporting consistency. 
  • Drive organizational adoption of PMO standards, tools, and best practices through coaching, training, documentation, and change management while mentoring Engineering Project Managers on governance and portfolio management practices. 
  • Build collaborative relationships and influence cross-functional stakeholders across Engineering, Software, Product Management, Quality, Regulatory, Clinical, Operations, Manufacturing, and Information Systems to improve organizational effectiveness and execution excellence. 
  • Support special projects and strategic initiatives as assigned.

Minimum Qualifications:

  • 8+ yrs of experience in regulated technical product development or technical project management

  • Experience developing and implementing project management methodologies, governance frameworks, and portfolio management processes

  • Experience supporting cross-functional engineering programs and portfolios

  • Experience developing executive dashboards, portfolio reporting, and performance metrics using Power BI or similar reporting tools

  • Experience using Jira, Confluence, and project or portfolio management platforms 

  • Strong analytical, organizational, communication, and problem-solving skills

  • Demonstrated ability to influence cross-functional stakeholders and drive alignment without direct authority

Preferred Qualifications:  

  • Medical device or other highly regulated industry experience 
  • Experience building, transforming, or maturing an Engineering PMO
  • Experience supporting integrated hardware, software, firmware, systems, or algorithm development programs
  • Experience with portfolio planning, engineering resource capacity planning, and investment prioritization
  • Experience supporting executive portfolio governance and strategic planning
  • PMP, PgMP, PMI-PMOCP, SAFe, Agile, Lean Six Sigma, or equivalent certification

Education: 

  • Bachelor's degree in Engineering, Engineering Management or related technical field required; advanced degree in Engineering, or related technical or business discipline preferred.

Language Requirements:

  • Ability to read, write, and communicate effectively in English
  • Ability to interpret technical documents, schematics, and written instructions
  • Ability to clearly document technical findings and communicate with cross-functional team members

Compensation + Benefits:  The anticipated range for this position is $160,000 - $180,000. Actual placement within the range is dependent on multiple factors, including but not limited to skills, education, and experience. This position also qualifies for up to 10% annual bonus based on Company, department, and individual performance. Masimo offers benefits such as Medical, Dental, Vision, Life/AD&D, Disability Insurance, 401(k), Vacation, Sick, Holiday, Paid Maternity Leave, Flexible Spending Accounts, voluntary Accident, Critical Illness, Hospital, Long-Term Care, Employee Assistance Program, Pet Insurance, on-site Wellness Clinic, Fitness Center, Cafe. All benefits are subject to eligibility requirements.

Physical requirements/Work Environment: 

This position primarily works in a laboratory environment. It requires frequent sitting, standing, and walking. Daily use of a computer and other computing and digital devices is required. May stand for extended periods when facilitating meetings or walking in the facilities.

The physical demands of the position described herein are essential functions of the job and employees must be able to successfully perform these tasks for extended periods. Reasonable accommodation may be made for those individuals with real or perceived disabilities to perform the essential functions of the job described.


Masimo logo

About Masimo

Sourced by ZipRecruiter

Industry

Medical equipment and supplies manufacturing

Company size

1,001 - 5,000 Employees

Headquarters location

Irvine, CA, US

Year founded

1989

Social media