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Fda Jobs in California (NOW HIRING)

Cesna Group

Junior Software Engineer

San Diego, CA · On-site

$50K - $100K/yr

This role involves close collaboration with Vision, Control, Mechanical, and X-Ray hardware teams to develop FDA-regulated medical imaging software. * The position primarily focuses on GUI ...

Amicis Global

SRE/ Devops Engineer

Mountain View, CA · On-site

$80 - $90/hr

You will ensure reliability, scalability, and compliance of critical systems in alignment with FDA GxP guidelines and HITRUST standards for healthcare data protection. You will lead initiatives in ...

Spyglass Pharma

Clinical Trial Associate

Aliso Viejo, CA · On-site

$90K - $110K/yr

Participate in FDA, Regulatory Agency, IRB/IEC meetings as needed. * Review of regulatory submissions, including clinical trial applications, IND, IDE, NDA, PMA, annual reports, CIB updates, meeting ...

Spyglass Pharma

Clinical Trial Associate

Aliso Viejo, CA · On-site

$35.50 - $48.50/hr

Participate in FDA, Regulatory Agency, IRB/IEC meetings as needed. * Review of regulatory submissions, including clinical trial applications, IND, IDE, NDA, PMA, annual reports, CIB updates, meeting ...

BiVACOR Inc

QC Inspector

Huntington Beach, CA · On-site

About the Role This is a high-impact, hands-on quality role in an FDA-regulated, Class III medical device environment, where your expertise will directly support the production of one of the most ...

Spyglass Pharma

Clinical Trial Associate

Aliso Viejo, CA

$35.50 - $48.50/hr

Participate in FDA, Regulatory Agency, IRB/IEC meetings as needed. * Review of regulatory submissions, including clinical trial applications, IND, IDE, NDA, PMA, annual reports, CIB updates, meeting ...

BiVACOR Inc

QC Inspector

Huntington Beach, CA · On-site

$22 - $35/hr

About the Role This is a high-impact, hands-on quality role in an FDA-regulated, Class III medical device environment, where your expertise will directly support the production of one of the most ...

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$13

$38

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How much do fda jobs pay per hour?

As of Aug 16, 2026, the average hourly pay for fda in California is $38.53, according to ZipRecruiter salary data. Most workers in this role earn between $24.01 and $48.02 per hour, depending on experience, location, and employer.

What qualifications do you need to work for the Food and Drug Administration?

To work for the Food and Drug Administration (FDA), candidates typically need a bachelor's degree in a relevant field such as science, engineering, or healthcare. Many positions require specialized knowledge, experience, or advanced degrees, and some roles may require professional certifications or licenses. Strong analytical skills, attention to detail, and familiarity with regulatory guidelines are also important.

What are some typical challenges faced by professionals working at the FDA, and how can they be managed?

Professionals at the FDA often navigate complex regulatory requirements, tight deadlines, and the need to balance public health priorities with industry innovation. Collaborating across multidisciplinary teams and staying updated on evolving scientific data are essential parts of the role. Adapting to frequent changes in policy and handling high volumes of submissions can be demanding, but leveraging strong communication skills and seeking mentorship within the agency can help manage these challenges effectively.

What are the key skills and qualifications needed to thrive as an FDA Regulatory Affairs Specialist, and why are they important?

To thrive as an FDA Regulatory Affairs Specialist, you need a strong background in life sciences, regulatory guidelines, and compliance, usually supported by a relevant degree such as pharmacy, biology, or chemistry. Familiarity with regulatory submission systems, FDA regulations (such as 21 CFR), and certifications like RAC (Regulatory Affairs Certification) are highly beneficial. Attention to detail, strong analytical thinking, and effective communication skills help professionals navigate complex regulations and collaborate with cross-functional teams. These competencies ensure that products meet legal requirements and safety standards, facilitating successful approvals and market access.

What does an FDA professional do?

An FDA professional works for the U.S. Food and Drug Administration, a federal agency responsible for protecting public health by ensuring the safety and efficacy of drugs, medical devices, food, cosmetics, and other products. Their roles can include reviewing and approving new drugs and medical devices, conducting inspections, enforcing regulations, and providing guidance to industries. FDA professionals may also work in research, policy development, and public outreach to ensure that products meet regulatory standards and are safe for consumer use.

What is the difference between Fda vs Food Scientist?

AspectFdaFood Scientist
Required CredentialsTypically a degree in health, science, or related field; certifications varyBachelor's or master's in food science, microbiology, or related
Work EnvironmentRegulatory agencies, laboratories, inspection sitesFood manufacturing facilities, laboratories, research settings
Employer & Industry UsageU.S. Food and Drug Administration, government agenciesFood companies, research institutions, government agencies
Common Search & Comparison IntentUnderstanding regulatory roles, compliance, and enforcementFood safety, product development, research

While both Fda professionals and Food Scientists work within the food industry, Fda roles focus on regulation, compliance, and enforcement of food safety laws, often within government agencies. Food Scientists primarily engage in research, product development, and ensuring food quality in manufacturing settings. The two careers overlap in food safety knowledge but differ in their primary responsibilities and work environments.

What are the most commonly searched types of Fda jobs in California?

The most popular types of Fda jobs in California are:

What are popular job titles related to Fda jobs in California?

For Fda jobs in California, the most frequently searched job titles are:

What job categories do people searching Fda jobs in California look for?

The top searched job categories for Fda jobs in California are:

What cities in California are hiring for Fda jobs?

Cities in California with the most Fda job openings:

Fda jobs near you
Infographic showing various Fda job openings in California as of August 2026, with employment types broken down into 61% Full Time, 13% Part Time, 13% Contract, and 13% Nights. Highlights an 100% In-person job distribution, with an average salary of $80,144 per year, or $38.5 per hour.

Junior Software Engineer

Cesna Group

San Diego, CA • On-site

$50K - $100K/yr

Full-time

Re-posted 4 days ago

Job description

Job Summary
  • We are seeking a Junior Software Engineer to join our Ez-X medical X-ray system development team. This role involves close collaboration with Vision, Control, Mechanical, and X-Ray hardware teams to develop FDA-regulated medical imaging software.
  • The position primarily focuses on GUI development (C#), C++ platform integration, and business logic implementation using our in-house software platform.
  • As medical device development is an iterative and highly regulated process, specific tasks and priorities may evolve based on project needs, regulatory requirements, and business objectives.
  • Candidates should have hands-on experience with C++. While prior experience with C# is not required, we are seeking individuals who are highly motivated and eager to learn new technologies.
Job Description
  • The responsibilities listed below describe the primary functions of this role but are not intended to be an exhaustive list. Additional responsibilities may be assigned as needed, provided they are consistent with the employee's role, skills, and professional experience.
  • - Develop and maintain C#-based GUI applications for medical X-ray systems
  • - Integrate algorithms developed by the Vision team into software components
  • - Implement business logic using the existing C++ software platform
  • - Display motor angle and system status information received from control boards
  • - Implement and test TXM board control interfaces
  • - Collaborate with cross-functional teams, including Vision, Control, Mechanical, and X-Ray hardware teams
  • - Participate in software verification and validation (V&V) activities required for FDA approval
  • - Identify, analyze, and fix software defects to improve system stability under the guidance of senior engineers
  • - Prepare and maintain technical documentation, test procedures, and test reports in compliance with FDA and internal quality requirements
Qualifications
  • Required Qualifications
  • - Bachelor's degree in Computer Science, Software Engineering, or related field
  • - 0?3 years of professional software development experience
  • - Basic knowledge of C++ (classes, memory management, STL)
  • - Familiarity with Windows-based application development
  • Preferred Qualifications
  • - Experience with C# and WPF/WinForms
  • - Experience with hardware-connected software (motors, sensors, boards)
  • - Basic understanding of medical imaging or X-ray systems
  • - Familiarity with multi-threaded programming
  • - Exposure to FDA or regulated software development environments
What's On Offer
  • - Opportunity to work on FDA-approved and next-generation medical devices
  • - Hands-on experience with real medical imaging systems
  • - Mentorship from senior engineers in medical and imaging domains
  • - Competitive salary and benefits (US market)
  • - Long-term career growth in regulated medical software development

Apply online or feel free to contact us directly for more information about the opportunity. Due to the high volume of applicant, we regret to inform that only shortlisted candidates will be notified. Thank you for your understanding.

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