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Fda Internship Jobs in California (NOW HIRING)

BRIDGEMED SOLUTIONS INC

Entry Level Biologist

Irvine, CA · On-site

$20 - $23/hr

... FDA and ISO 13485 quality system requirements Qualifications Required:  Bachelor's degree in ... or regulated lab environment (internships welcome)  Strong attention to detail and ...

BRIDGEMED SOLUTIONS INC

Entry Level Biologist

Irvine, CA · On-site

$20 - $23/hr

... FDA and ISO 13485 quality system requirements Qualifications Required:  Bachelor's degree in ... or regulated lab environment (internships welcome)  Strong attention to detail and ...

BRIDGEMED SOLUTIONS INC

Entry Level Biologist

Irvine, CA · On-site

$20 - $23/hr

... FDA and ISO 13485 quality system requirements Qualifications Required:  Bachelor's degree in ... or regulated lab environment (internships welcome)  Strong attention to detail and ...

Argen Corporation

Argen Intern

San Diego, CA · On-site

$18.25/hr

Argen's products are FDA regulated and ISO certified. About the Opportunity Argen Interns are provided a great opportunity to learn more about their field of study. The internship will both challenge ...

Masimo

Cybersecurity Quality Engineer

Irvine, CA · On-site

$85K - $105K/yr

... internship, co-op, or project-based experience in regulated environments will be considered ... Familiarity with FDA 21 CFR Part 820, ISO 13485, ISO 14971, FDA cybersecurity guidance, or related ...

Masimo

Cybersecurity Quality Engineer

Irvine, CA · On-site

$85K - $105K/yr

... internship, co-op, or project-based experience in regulated environments will be considered ... Familiarity with FDA 21 CFR Part 820, ISO 13485, ISO 14971, FDA cybersecurity guidance, or related ...

EMSAR

Field Service Engineer I

Palo Alto, CA · On-site

$28 - $33/hr

FDA field change orders ("recalls") * Bench repair and remanufacturing * Installation * Call center ... internship, externship, apprentice is acceptable) * Valid driver license and liability insurance

EMSAR

Field Service Engineer I

Palo Alto, CA

$28 - $33/hr

FDA field change orders ("recalls") * Bench repair and remanufacturing * Installation * Call center ... internship, externship, apprentice is acceptable) * Valid driver license and liability insurance

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Fda Internship information

What is an FDA internship?

An FDA Internship is a temporary position designed for students or recent graduates to gain hands-on experience in regulatory science, public health, and policy. Interns work on projects related to drug approval, food safety, medical devices, and other areas overseen by the U.S. Food and Drug Administration. These internships provide valuable exposure to federal regulations, research, and compliance processes. Opportunities may be available in various FDA offices and centers, offering mentorship and professional development.

What kinds of projects or tasks do FDA interns typically work on during their internship?

FDA interns often work on a variety of projects related to public health, regulatory policy, scientific research, or data analysis, depending on their department. Interns may assist with laboratory studies, analyze clinical trial or adverse event data, contribute to policy reviews, or help draft scientific reports and communications. Supervision and mentorship are typically provided by experienced professionals, and interns often have opportunities to attend seminars or networking events. This hands-on experience provides valuable practical insight into the federal regulatory process and helps interns build skills for future careers in science or public health.

What are the key skills and qualifications needed to thrive in the FDA internship position, and why are they important?

To thrive as an FDA Intern, you generally need a background in life sciences, public health, pharmacy, or a related field, along with strong analytical and research skills. Familiarity with data analysis tools, laboratory techniques, or regulatory databases is often beneficial depending on the specific internship focus. Excellent written and verbal communication, attention to detail, and the ability to work collaboratively in multidisciplinary teams are stand-out soft skills. These attributes are crucial for meeting the FDA's standards for study integrity, regulatory compliance, and effective information sharing within complex projects.

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 Internship jobs in California? For Fda Internship jobs in California, the most frequently searched job titles are:
What job categories do people searching Fda Internship jobs in California look for? The top searched job categories for Fda Internship jobs in California are:
What cities in California are hiring for Fda Internship jobs? Cities in California with the most Fda Internship job openings:
Fda Internship jobs near you
Infographic showing various Fda Internship job openings in California as of August 2026, with employment types broken down into 8% Internship, 2% As Needed, 67% Full Time, 11% Part Time, 6% Temporary, and 6% Contract. Highlights an 96% In-person, 2% Hybrid, and 2% Remote job distribution.

Operations Internship - Labeling Process & Formulation Laboratory

Cordis

Irvine, CA • On-site

$24/hr

Full-time

Posted 13 days ago

Job description

Overview
Selution, in partnership with Cordis, specializes in the development of ground-breaking technology and commercialization of advanced drug device combination products for the treatment of coronary and peripheral artery disease. Our mission is to revolutionize healthcare by creating next-generation solutions that address unmet and critical medical needs.
Responsibilities
The Operations Intern will support daily activities within the Labeling Process and Formulation Laboratory to ensure manufacturing operations comply with quality standards, regulatory requirements, and production schedules. This 6-month internship provides hands-on exposure to medical device manufacturing, documentation practices, quality systems, and laboratory operations in a regulated environment.
Key Responsibilities
Labeling Process
  • Assist with the preparation, verification, and issuance of product labels in accordance with approved procedures and regulatory requirements.
  • Support label reconciliation, inspection, and documentation activities.
  • Verify label accuracy, including product information, lot numbers, expiration dates, and barcode readability.
  • Participate in label change control and document revision processes.
  • Help maintain compliance with Good Documentation Practices (GDP) and Standard Operating Procedures (SOPs).

Formulation Laboratory
  • Assist laboratory personnel in preparing formulations, solutions, and materials according to established procedures.
  • Support laboratory testing, sample preparation, and data collection activities.
  • Maintain laboratory equipment cleanliness, calibration records, and inventory of chemicals and consumables.
  • Record experimental observations and maintain accurate laboratory documentation.
  • Follow laboratory safety protocols and Good Laboratory Practices (GLP).

Operations Support
  • Support production documentation, and quality records.
  • Collaborate with Manufacturing, Quality Assurance, Regulatory Affairs, and Engineering teams.
  • Perform other operational and administrative duties as assigned.

Qualifications
Required Qualifications
  • Currently pursuing a bachelor's degree in a related scientific discipline.
  • Strong interest in medical device manufacturing and regulated industries.
  • Basic understanding of laboratory practices and manufacturing operations.
  • Familiarity with Microsoft Office Suite (Excel, Word, PowerPoint).
  • Excellent organizational, analytical, and communication skills.
  • Ability to work independently and collaboratively in a team environment.
  • High attention to detail and commitment to quality and compliance.

Preferred Qualifications
  • Knowledge of ISO 13485, FDA Quality System Regulation (21 CFR Part 820), or Good Manufacturing Practices (GMP).
  • Experience with laboratory techniques or manufacturing environments through coursework or previous internships.
  • Exposure to Lean Manufacturing or Six Sigma concepts is an advantage.

Learning Outcomes
By the end of the internship, the intern will gain experience in:
  • Medical device manufacturing operations
  • Labeling compliance and documentation control
  • Formulation laboratory procedures
  • Quality Management Systems (QMS)
  • Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP)
  • Cross-functional collaboration within a regulated medical device environment
  • Continuous improvement and operational excellence principles

This description reflects responsibilities commonly assigned to operations interns in FDA- and ISO-regulated medical device manufacturing environments while providing meaningful exposure to both production labeling and laboratory processes
Pay / Compensation - The expected pre-tax pay rate for this position is $24 hourly
US work authorization is a precondition of employment. The company will not consider candidates who require sponsorship for a work-authorized visa.
Preferred Qualifications
Cordis is proud to be an equal opportunity employer and is committed to providing equal opportunity for all teammates and applicants. At Cordis, our teammates all bring different strengths, experiences, and backgrounds, who share a passion for improving people's lives. Diversity not only includes race and gender identity, but also age, disability status, veteran status, sexual orientation, religion, and many other parts of one's identity. All our teammates' points of view are key to our success, and we believe inclusion is everyone's responsibility. Together, we strive to create and maintain working and learning environments that are inclusive, equitable and welcoming.

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