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Regulatory Jobs in Riverside, CA (NOW HIRING)

Kaygen Inc

Coord 3, Regulatory Affairs

Irvine, CA · On-site

Regulatory Affairs Coordinator 3 (Contract) Duration: 6 months, with option to extend We are seeking a highly detail-oriented and accountable Regulatory Affairs Coordinator 3 to support key ...

Collabera

Assoc Regulatory Affairs Spec

Irvine, CA · On-site

The Regulatory Affairs Admin/Coordinator is a key position in regulatory affairs as this individual will provide the necessary administrative and coordination support to the Global Regulatory Affairs ...

Alcon

Regulatory Affairs Manager I

Lake Forest, CA · On-site

The Manager I, Regulatory Affairs Strategy (Professional Path) ), reporting to the Senior Manager of Regulatory Affairs (LLSI), is primarily responsible for coordinating regulatory affairs activities ...

Kaygen Inc.

Coord 3, Regulatory Affairs

Irvine, CA · On-site

Regulatory Affairs Coordinator 3 (Contract) Duration: 6 months, with option to extend We are seeking a highly detail-oriented and accountable Regulatory Affairs Coordinator 3 to support key ...

Alcon

Director, Regulatory Affairs Strategy

Lake Forest, CA · On-site

$159K - $210K/yr

The Regulatory Strategy job family covers roles responsible for developing and implementing strategies to obtain and maintain product approvals from regulatory agencies in support of Alcon ...

Masimo

Sr Regulatory Affairs Specialist

Irvine, CA · On-site

$85K - $130K/yr

Job Summary Sr Regulatory Affairs Specialist is an accomplished regulatory professional with a successful work history with leading regulatory initiatives and partnering with Sales and Marketing ...

Alcon

Director, Regulatory Affairs Strategy

Lake Forest, CA · On-site

$159K - $210K/yr

As a Director, Regulatory Affairs Strategy (Management Path) supporting Alcon's Quality & Regulatory Affairs organization, this onsite role based at our Lake Forest, California main campus is ...

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Showing results 21-40

All JobsRegulatory JobsRegulatory Jobs in Riverside, CA

Regulatory information

See Riverside, CA salary details

$19

$41

$65

How much do regulatory jobs pay per hour?

As of Aug 8, 2026, the average hourly pay for regulatory in Riverside, CA is $41.28, according to ZipRecruiter salary data. Most workers in this role earn between $33.12 and $48.89 per hour, depending on experience, location, and employer.

What are some common challenges faced in a regulatory role, and how can they be addressed?

Professionals in Regulatory roles often face the challenge of keeping up with constantly evolving laws and industry standards. Staying current requires ongoing education, close collaboration with legal teams, and proactive monitoring of regulatory updates. Additionally, balancing compliance requirements with business goals can be complex, so strong communication and problem-solving skills are essential. Building relationships with internal departments and regulatory agencies can help streamline processes and ensure timely responses to regulatory changes.

What are the key skills and qualifications needed to thrive in a regulatory role, and why are they important?

To thrive in a Regulatory role, you need a strong understanding of compliance frameworks, regulatory guidelines, and industry standards, often supported by a degree in law, life sciences, or a related field. Familiarity with regulatory submission systems, document management tools, and certifications such as RAC (Regulatory Affairs Certification) are advantageous. Attention to detail, analytical thinking, and effective communication are critical soft skills for managing regulatory processes and liaising with authorities. These abilities ensure timely approvals, minimize compliance risks, and support organizational reputation and market access.

What is a regulatory job?

A regulatory job involves ensuring that organizations comply with laws, regulations, and standards relevant to their industry. Professionals in this field often review policies, prepare documentation, and work with government agencies to maintain compliance, requiring knowledge of legal requirements and attention to detail.

What is the difference between Regulatory vs Compliance Officer?

AspectRegulatoryCompliance Officer
Required CredentialsRegulatory certifications, industry-specific licensesCompliance certifications, such as CCEP or CRCM
Work EnvironmentRegulatory agencies, government bodies, legal teamsCorporate offices, compliance departments, financial institutions
Employer & Industry UsageUsed in industries like healthcare, finance, manufacturingCommon in banking, insurance, healthcare sectors
Search & Comparison IntentUnderstanding regulatory roles, legal complianceEnsuring company adherence to policies, internal audits

While both roles focus on adherence to rules, Regulatory professionals primarily interpret and implement government regulations, often working with legal and government entities. Compliance Officers focus on internal policies and procedures to ensure their organization meets legal and ethical standards. Both roles are essential for risk management but differ in scope and focus.

What are the most commonly searched types of Regulatory jobs in Riverside, CA? The most popular types of Regulatory jobs in Riverside, CA are:
What are popular job titles related to Regulatory jobs in Riverside, CA? For Regulatory jobs in Riverside, CA, the most frequently searched job titles are:
What job categories do people searching Regulatory jobs in Riverside, CA look for? The top searched job categories for Regulatory jobs in Riverside, CA are:
What cities near Riverside, CA are hiring for Regulatory jobs? Cities near Riverside, CA with the most Regulatory job openings:
Regulatory jobs near you
Infographic showing various Regulatory job openings in Riverside, CA as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 13% Part Time, and 4% Contract. Highlights an 91% Physical, 3% Hybrid, and 6% Remote job distribution, with an average salary of $85,868 per year, or $41.3 per hour.

Specialist, Regulatory Affairs Surgical

Edwards Lifesciences Corporation

Irvine, CA • On-site

$74K - $104K/yr

Full-time

Re-posted 10 days ago

Edwards Lifesciences rating

8.3

Company rating: 8.3 out of 10

Based on 30 frontline employees who took The Breakroom Quiz

67th of 537 rated manufacturers

Job description

Make a meaningful difference to patients around the world. From design to production, our Regulatory Affairs teams help guide our innovative technologies through complex domestic and international regulatory environments. Working in partnership with external government and regulatory authorities, and alongside diverse internal stakeholders, your close attention to detail and technical mastery will help ensure our products reach clinicians and improve patients' lives.

Dedicated to innovation, our Surgical business unit is focused on identifying and solving critical, unmet needs in cardiac surgery. In understanding the challenges of open-heart surgery, we partner with surgical teams to deliver modern technologies intended to enhance patients' quality of life and expand their potential treatment opportunities. It's our driving force to help patients live longer and healthier lives. Join us and be part of our inspiring journey.

How you will make an impact:

  • Represent the regulatory function on manufacturing and product development teams to provide input on regulatory requirements, including presenting alternatives for meeting regulatory requirements and resolving conflicts between those requirements and development issues, and/or reporting to management

  • Prepare and oversee documentation packages for submission to global regulatory agencies. Track timelines and documents milestone achievements for inclusion in regulatory submissions. May interact with regulatory agencies as part of submission review and on-site audit support (e.g., IDE's, PMA's, annual reports, 510(k)'s, STED's and CE marking design dossiers and technical files)

  • Provide guidance on regulatory requirements necessary for contingency planning

  • Monitor proposed and current global regulations and guidance; assesses impact of such regulations and guidance on assigned project(s); proposes suggestions on utilizing regulatory updates to expedite approval process

  • Review labeling content, product and process changes, and product documentation to assure regulatory requirements compliance, consistency, and accuracy

  • Prepare documents for submissions, including assuring the appropriate forms for all of the global regulatory bodies; assist with GUDID submissions

What you will need (Required):

  • Bachelor's Degree & a minimum of 3 years related experience or equivalent experience based on Edwards criteria

  • Coursework, seminars, and/or other formal government and/or trade association training

What else we look for (Preferred):

  • Bachelor's Degree in scientific discipline (e.g., Biology, Microbiology, Chemistry, Bioengineering)

  • Experience in preparing domestic and international product submissions

  • Solid knowledge and understanding of global regulations relevant to medical devices, Class II and/or Class III devices

  • Solid knowledge and understanding of global regulatory requirements for new products or product changes

Aligning our overall business objectives with performance, we offer competitive salaries, performance-based incentives, and a wide variety of benefits programs to address the diverse individual needs of our employees and their families.
For California, the base pay range for this position is $74,000 - $104,000 (highly experienced).
The pay for the successful candidate will depend on various factors (e.g., qualifications, education, prior experience). Applications will be accepted while this position is posted on our Careers website.

#LI-Onsite

Edwards is an Equal Opportunity/Affirmative Action employer including protected Veterans and individuals with disabilities.

COVID Vaccination Requirement

Edwards is committed to protecting our vulnerable patients and the healthcare providers who are treating them. As such, all patient-facing and in-hospital positions require COVID-19 vaccination. If hired into a covered role, as a condition of employment, you will be required to submit proof that you have been vaccinated for COVID-19, unless you request and are granted a medical or religious accommodation for exemption from the vaccination requirement. This vaccination requirement does not apply in locations where it is prohibited by law to impose vaccination.

What Edwards Lifesciences employees say

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Benefits

Hours and flexibility

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About Edwards Lifesciences

Sourced by ZipRecruiter

Edwards Lifesciences is the global leader in patient-focused medical innovations for structural heart disease, as well as critical care and surgical monitoring. Driven by a passion to help patients, the company collaborates with the world's leading clinicians and researchers to address unmet healthcare needs, working to improve patient outcomes and enhance lives. Headquartered in Irvine, California, Edwards Lifesciences has extensive operations in North America, Europe, Japan, Latin America and Asia and currently employs over 15,000 individuals worldwide. For us, helping patients is not a slogan - it's our life's work. From developing devices that replace or repair a diseased heart valve to creating new technologies that monitor vital signs in the critical care setting, we focus on helping patients regain and improve the quality of their life.

Industry

Medical equipment and supplies manufacturing

Company size

10,000+ Employees

Headquarters location

Irvine, CA, US

Year founded

1958

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