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Quality Regulatory Manager Jobs in Riverside, CA

Strong knowledge of Quality Management Systems (QMS) principles and regulated quality processes. * Deep understanding of applicable regulatory and industry requirements, including but not limited to:

Strong knowledge of Quality Management Systems (QMS) principles and regulated quality processes. * Deep understanding of applicable regulatory and industry requirements, including but not limited to:

Showing results 21-40

Quality Regulatory Manager information

See Riverside, CA salary details

$25K

$89.9K

$164.8K

How much do quality regulatory manager jobs pay per year?

As of Aug 20, 2026, the average yearly pay for quality regulatory manager in Riverside, CA is $89,887.00, according to ZipRecruiter salary data. Most workers in this role earn between $45,900.00 and $141,900.00 per year, depending on experience, location, and employer.

What is a quality regulatory manager?

A Quality Regulatory Manager is a professional responsible for ensuring that a company's products and processes comply with industry regulations, standards, and quality requirements. They oversee the implementation of quality management systems, prepare for regulatory audits, and keep the organization updated on changing regulations. This role often involves working closely with various departments to ensure documentation, processes, and products meet both internal and external compliance standards. Quality Regulatory Managers play a critical part in maintaining the company's reputation and ability to operate within legal guidelines.

How does a quality regulatory manager typically collaborate with cross-functional teams to ensure compliance?

A Quality Regulatory Manager works closely with departments such as manufacturing, R&D, and supply chain to interpret and implement regulatory requirements across the organization. Regular meetings and clear communication are essential to align quality systems with evolving regulations and address compliance gaps. The manager often leads training sessions, reviews documentation, and coordinates audits, ensuring all teams understand and adhere to quality standards. This collaborative approach helps maintain product safety and supports successful regulatory submissions.

What are the key skills and qualifications needed to thrive as a quality regulatory manager, and why are they important?

To thrive as a Quality Regulatory Manager, you need in-depth knowledge of quality management systems, regulatory compliance, and industry standards, typically backed by a relevant degree and experience in regulated environments. Familiarity with ISO standards, FDA regulations, audit management tools, and certifications like CQE or RAC is highly valued. Strong analytical thinking, attention to detail, and effective communication are critical soft skills for collaborating across departments and ensuring compliance. These skills and qualifications are essential to maintain product quality, meet regulatory requirements, and mitigate compliance risks within an organization.

What is the difference between Quality Regulatory Manager vs Quality Assurance Specialist?

AspectQuality Regulatory ManagerQuality Assurance Specialist
CertificationsISO 13485, Regulatory Affairs certificationsISO 9001, QA certifications
Work EnvironmentRegulatory agencies, compliance departmentsManufacturing, production, quality labs
Employer & Industry UsageMedical devices, pharmaceuticals, biotechManufacturing, consumer products, electronics

The Quality Regulatory Manager focuses on ensuring products meet regulatory standards and manages compliance documentation, often working closely with regulatory agencies. In contrast, the Quality Assurance Specialist primarily ensures product quality through testing and process audits. Both roles require quality certifications but differ in their focus areas and work environments.

What job categories do people searching Quality Regulatory Manager jobs in Riverside, CA look for?

The top searched job categories for Quality Regulatory Manager jobs in Riverside, CA are:

What cities near Riverside, CA are hiring for Quality Regulatory Manager jobs?

Cities near Riverside, CA with the most Quality Regulatory Manager job openings:

Infographic showing various Quality Regulatory Manager job openings in Riverside, CA as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 14% Part Time, 4% Contract, and 1% Nights. Highlights an 88% Physical, 2% Hybrid, and 10% Remote job distribution, with an average salary of $89,887 per year, or $43.2 per hour.

Senior Regulatory Affairs Associate

Alcon

Lake Forest, CA • On-site

Full-time

Medical, Life, Retirement, PTO

Re-posted 6 hours ago


Alcon rating

7.5

Company rating: 7.5 out of 10

Based on 70 frontline employees who took The Breakroom Quiz

235th of 542 rated manufacturers


Job description

At Alcon, we're passionate about enhancing sight and helping people see brilliantly. With more than 25,000 associates, we innovate fearlessly, champion progress, and act swiftly to impact global eye health. We foster an inclusive culture, recognizing your contributions and offering opportunities to grow your career like never before. Together, we make a difference in the lives of our patients and customers. Are you ready to join us?
This role is part of Alcon's Quality & Regulatory Affairs function, a team that ensures our products are in compliance with global, local, and internal regulations and meet the strictest standards of quality as we help people see brilliantly. The Sr. Associate, Regulatory Affairs Strategy (Professional Path) , reporting to the Senior Manager of Regulatory Affairs (LLSI), is primarily responsible for coordinating regulatory compliance for Alcon's product portfolio, managing local initiatives, and supporting business requests for product and regulatory information. You will also participate in cross-functional teams for risk management and produce compliance metrics. Occasionally, you will represent the Regulatory Affairs Manager, when requested.
In this role, a typical day will include:
  • Operational support / execution tasks associated with LCM work
    • Working with Reg. Ops. to complete user fee requests
    • Data requests to R&D for tender applications, one-off requests for country-specific technical information, maintenance of project status master slide deck for regional RA calls, drafting (not signing) explanation letters, and other administrative requirements for HA queries
  • Perform specialized tasks and conduct independent research within the Regulatory Affairs Strategy team to optimize outcomes and contribute to project goals
  • Coordinate product submissions, renewals, and updates by liaising with plants, agents, and authorities to ensure timely submissions and approvals
  • Oversee promotional material approval for Alcon ME/KSA portfolio, ensuring ethical conduct and compliance with laws, codes, and regulations
  • Provide regulatory strategies for new product introductions and changes, maintaining compliance to drive competitive advantage
  • Support medical device and/or pharmaceutical products, ensuring adherence to relevant regulations
  • Adhere to Good Practice (GxP) regulations by following Standard Operating Procedures (SOPs), maintaining documentation, ensuring quality control, and completing required training
  • ROW submissions for new projects, with supervision
  • Assistance with LCM work, with supervision
    • Change assessments / RIARs
    • PPRR work, registration renewals, TF maintenance, etc.
  • Operational support / execution tasks associated with LCM work
    • Working with Reg. Ops. to complete user fee requests
    • Data requests to R&D for tender applications, one-off requests for country-specific technical information, maintenance of project status master slide deck for regional RA calls, drafting (not signing) explanation letters, and other administrative requirements for HA queries

WHAT YOU'LL BRING TO ALCON:
  • Bachelor's Degree or Equivalent years of directly related experience (or high school +10 yrs; Assoc.+16yrs; M.S.+0 yrs) The ability to fluently read, write, understand and communicate in English
  • 2 Years of Relevant Experience
  • 1 Years of Demonstrated Leadership
  • Location: Onsite Lake Forest, CA
  • Travel Requirements: 0 - 10%
  • Relocation Assistance: Not Available
  • Sponsorship Available: Not Available

HOW YOU CAN THRIVE AT ALCON:
  • Collaborate with teammates to share standard processes and learnings as work evolves!
  • See your career like never before with focused growth and development opportunities
  • Join Alcon's mission to provide outstanding, innovative products and solutions to improve sight, improve lives, and grow your career!
  • Alcon provides robust benefits package including health, life, retirement, flexible time off for exempt associates, PTO for hourly associates, and much more!

Alcon Careers
See your impact at alcon.com/careers
ATTENTION: Current Alcon Employee/Contingent Worker
If you are currently an active employee/contingent worker at Alcon, please click the appropriate link below to apply on the Internal Career site.
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Compensation and Benefits
Alcon's Total Rewards programs are designed to align incentives with business objectives, support our values, and deliver long-term value. Our compensation approach includes a combination of fixed and variable pay, with short-term and long-term incentive opportunities for eligible roles. Our benefits offerings are designed to support associates and their families across key life events, including programs that promote health and well-being, provide financial security, and support retirement planning.
The salary range posted represents the anticipated hiring range for this role. Actual compensation may vary based on factors such as experience, skills, location, and internal equity, and may fall outside the posted range.
Pay Range
102,850.00 - 133,100.00
Pay Frequency
Annual
Alcon is an Equal Opportunity Employer and participates in E-Verify. Alcon takes pride in maintaining a diverse environment and our policies are not to discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, gender identity, marital or veteran status, disability, or any other legally protected status. Alcon is also committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please send an email to alcon.recruitment@alcon.com and let us know the nature of your request and your contact information.

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