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Regulatory Jobs in Riverside, CA (NOW HIRING)

Collabera

Assoc Regulatory Affairs Spec

Irvine, CA

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

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 ...

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 ...

Prismatik

Regulatory Affairs Specialist, Sr.

Irvine, CA · On-site

$84K - $120K/yr

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.

Prismatik

Regulatory Affairs Specialist, Sr.

Irvine, CA · On-site

$84K - $120K/yr

Maintains knowledge on current regulations and guidelines. * Evaluates compliance with applicable regulations, project policies, and procedures * Reviews and writes standard operating procedures ...

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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 Jun 14, 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.

Which is better, RA or QA?

Regulatory Affairs (RA) and Quality Assurance (QA) are distinct roles in the healthcare and manufacturing industries. RA focuses on ensuring products comply with regulations and obtaining approvals, often requiring knowledge of regulations and documentation skills, while QA emphasizes maintaining product quality through testing, audits, and process improvements. Both roles are essential, and the choice depends on your interest in compliance versus quality management.

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 jobs pay 500,000 a year in the US?

In the regulatory field, senior roles such as Chief Compliance Officers, regulatory directors, and senior legal counsel can reach or exceed $500,000 annually, especially in large corporations or financial institutions. These positions typically require extensive experience, advanced certifications, and strong leadership skills. Compensation varies based on industry, company size, and geographic location.

What does a regulatory job do?

A regulatory job involves ensuring that a company's products, services, or operations comply with government laws, industry standards, and internal policies. Professionals in this field review documentation, prepare reports, and may interact with regulatory agencies to maintain compliance and obtain necessary approvals. Strong knowledge of relevant regulations and attention to detail are essential skills in this role.

Will AI replace regulatory affairs?

AI is unlikely to fully replace regulatory affairs professionals, as the role requires complex judgment, interpretation of regulations, and communication skills that AI cannot replicate. Instead, AI tools can assist with data analysis, document review, and compliance tracking, enhancing efficiency. Regulatory professionals will continue to play a vital role in ensuring adherence to evolving regulations and providing strategic guidance.

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
Specialist, Regulatory Affairs Surgical

Specialist, Regulatory Affairs Surgical

Edwards Lifesciences Corporation

Irvine, CA

$74K - $104K/yr

Full-time

Posted 16 days ago

Edwards Lifesciences rating

8.3

Company rating: 8.3 out of 10

Based on 30 frontline employees who took The Breakroom Quiz

65th of 518 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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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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