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Fda Entry Level Jobs in California (NOW HIRING)

... FDA regulated biopharmaceutical environments. The role coordinates all validation activities by ... (entry-level qualifications) to $98,000 (highly experienced) annually The application window is ...

... for entry-level; 2+ years commonly expected for full technician roles. * Familiarity with relevant standards (ISO, GMP, FDA) depending on industry. (Qualifications aggregated from job-market ...

02203A - Technician, QA

Fresno, CA · On-site

$17 - $18/hr

... for entry-level; 2+ years commonly expected for full technician roles. * Familiarity with relevant standards (ISO, GMP, FDA) depending on industry. (Qualifications aggregated from job-market ...

02203A - Technician, QA

Fresno, CA · On-site

$17 - $18.25/hr

... for entry-level; 2+ years commonly expected for full technician roles. * Familiarity with relevant standards (ISO, GMP, FDA) depending on industry. (Qualifications aggregated from job-market ...

Pharmacist I

Antioch, CA · On-site

$85 - $104.96/hr

... USP , FDA regulations (such as the DSCSA), California Business and Professions Codes, OSHA ... Position is entry level and requires 0-3 years' experience as a registered pharmacist required.

Pharmacist I

Antioch, CA · On-site

$85 - $104.96/hr

... USP , FDA regulations (such as the DSCSA), California Business and Professions Codes, OSHA ... Position is entry level and requires 0-3 years' experience as a registered pharmacist required.

Pharmacist I

Antioch, CA · On-site

$85 - $104.96/hr

... USP , FDA regulations (such as the DSCSA), California Business and Professions Codes, OSHA ... Position is entry level and requires 0-3 years' experience as a registered pharmacist required.

HME Delivery Driver

Sacramento, CA · On-site

$17.50 - $22/hr

The Home Medical Equipment (HME) Delivery Driver is an entry level position whose primary ... OSHA, NFPA, FDA and DOT regulations. The HME Delivery Driver operates vehicles in a safe ...

HME Delivery Driver

Santa Fe Springs, CA · On-site

$17 - $21.25/hr

The Home Medical Equipment (HME) Delivery Driver is an entry level position whose primary ... OSHA, NFPA, FDA and DOT regulations. The HME Delivery Driver operates vehicles in a safe ...

HME Delivery Driver

Hayward, CA · On-site

$16 - $23/hr

The Home Medical Equipment (HME) Delivery Driver is an entry level position whose primary ... OSHA, NFPA, FDA and DOT regulations. The HME Delivery Driver operates vehicles in a safe ...

... FDA and GMP compliance. What You'll Work On * Assure compliance with corporate and divisional ... Lead, coach, and mentor non-exempt and entry level exempt personnel on quality principles and ...

Showing results 41-60

Fda Entry Level information

What are the typical responsibilities of an FDA entry level?

In an FDA Entry Level role, you may be tasked with supporting regulatory submissions, compiling and reviewing documentation, and ensuring compliance with FDA guidelines. Your responsibilities might also include data entry, assisting with laboratory tests or inspections, and helping prepare reports for internal and external stakeholders. You could work closely with scientists, regulatory affairs specialists, and quality assurance teams, which provides valuable exposure to the regulatory process and industry best practices. This hands-on experience helps you build foundational knowledge and opens the door to advancement to more specialized or senior roles over time.

What are the key skills and qualifications needed for an FDA entry level?

To thrive in an FDA Entry Level position, candidates typically need a bachelor’s degree in life sciences, pharmacy, or a related field, along with basic knowledge of regulatory processes. Familiarity with regulatory documentation, data entry systems, and software like Microsoft Office is important and some roles may require training in Good Laboratory Practice (GLP) or similar certifications. Detail orientation, analytical thinking, and strong written and verbal communication skills help candidates excel and collaborate effectively. These competencies ensure accuracy, compliance, and smooth communication in highly regulated environments.

What qualifications do I need for FDA entry level jobs?

FDA entry-level jobs typically require a bachelor's degree in a relevant field such as biology, chemistry, or health sciences. Strong attention to detail, good communication skills, and familiarity with regulatory guidelines and documentation are also important qualifications.

What is an FDA entry level?

An FDA entry-level job is a starting position within the U.S. Food and Drug Administration, typically suited for recent graduates or individuals with minimal experience in regulatory affairs, public health, or scientific research. These roles can include positions in drug evaluation, food safety, compliance, and laboratory research. Responsibilities often involve data analysis, regulatory review, inspections, and assisting senior staff with policy implementation. Entry-level professionals gain valuable experience in federal regulations, public health policies, and scientific evaluations, which can lead to career advancement within the agency.

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 Entry Level jobs in California?

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

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

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

What cities in California are hiring for Fda Entry Level jobs?

Cities in California with the most Fda Entry Level job openings:

Infographic showing various Fda Entry Level job openings in California as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution.

Validation Engineer I

NKW NantKwest Inc

El Segundo, CA • On-site

$98K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 4 days ago


Job description

Company Overview
ImmunityBio, Inc. (NASDAQ: IBRX) is a commercial-stage biotechnology company developing cell and immunotherapy products that are designed to help strengthen each patient's natural immune system, potentially enabling it to outsmart the disease and eliminate cancerous or infected cells. We envision a day when we no longer fear cancer, but can conquer it, thanks to the biological wonder that is the human immune system. Our scientists are working to develop novel therapies that harness that inherent power by amplifying both branches of the immune system, attacking cancerous or infected cells today while building immunological memory for tomorrow. The goal: to reprogram the patient's immune system and treat the host rather than just the disease.
Why ImmunityBio?
ImmunityBio is developing cutting-edge technology with the goal to transform the lives of patients with cancer and develop next-generation therapies and vaccines that complement, harness and amplify the immune system to defeat cancers and infectious diseases.
Opportunity to join a publicly traded biopharmaceutical company with headquarters in Southern California.
Work with a collaborative team with the ability to work across different areas of the company.
Ability to join a growing company with professional development opportunities.

Position Summary

The Validation Engineer I is responsible for generating and executing protocols, creating summary reports and executing validation activities in FDA regulated biopharmaceutical environments. The role coordinates all validation activities by constant communication with affected departments and personnel. The Validation Engineer I works on projects and matters of minimal complexity in a support role and works closely with senior staff.

Essential Functions

  • Support collaboration with cross-functional departments, clients, CMOs, and vendors to meet project and company expectations and objectives.
  • Assist in perform validation activities for equipment, utility systems, facilities, processes, and automation systems in compliance with approved SOPs, cGMPs, and applicable regulatory requirements.
  • Generate, support and execute validation protocols (IQ/OQ/PQ/CV/PV) of all site equipment including laboratory equipment, production equipment, utilities (as applicable) and other related systems in an FDA regulated environment,
  • Generate and keep current inventory of GMP systems and requalification/periodic reviews schedules.,
  • Perform risk assessments for GMP systems as required.
  • Plan validation efforts according to risk.
  • Troubleshoot discrepancies reported during validation/qualification and assist senior engineers with resolutions.
  • Support the Validation team purchasing acquisitions and oversee the supplies and equipment inventory as needed.
  • Adhere to Standard Operating Procedures (SOPs), process improvements, and standardization of templates.
  • Performs ad-hoc and cross-functional duties and/or projects assigned to support business needs and provide developmental opportunities.

Basic Qualifications

  • Bachelor's degree in a science or related discipline is required.
  • 1+ years of relevant validation or GMPregulated industry experience is required.
  • Experience with facility commissioning and validation of equipment and facilities is required.

Preferred Qualifications

  • Good technical document writing and reviewing with teams
  • Good understanding and application of validation principles, concepts, practices, and industry standards.
  • Working knowledge of validation principles including commissioning, IQ/OQ/PQs related to equipment and facilities
  • Working knowledge of related quality systems such as change control; CAPA (including deviations/OOSs); training and document control is required.
  • Working knowledge of GMPs, OSHA compliance, 21 CFR Part 11 and cleanrooms, automated biopharmaceutical processing and plant equipment
  • Good interpersonal skills and the ability to work well independently and in a team environment
  • Good communication and organizational skills

Working Environment / Physical Environment

  • This position works on-site.
  • Exposure to onsite in-lab environment
  • Must be able to don and wear Personal Protective Equipment (PPE) as required
  • Lifting, standing, climbing, bending, grasping, sitting, pulling, pushing, stooping, stretching, and carrying are generally required to perform the functions of this position
  • Must possess mobility to work in a standard office setting and to use standard office equipment, including a computer.
  • Must be able to lift frequently lift up to 35 pounds and occasionally lift/move 50 pounds

This position is eligible for a discretionary bonus and equity award. The annual base pay range for this position is below. The specific rate will depend on the successful candidate's qualifications, prior experience as well as geographic location.

$88,200 (entry-level qualifications) to $98,000 (highly experienced) annually

The application window is anticipated to close on 60 days from when it is posted or sooner if the position is filled or closed.

ImmunityBio employees are as valuable as the people we serve. We have built a resource of robust benefit offerings to best support the total wellbeing of our team members and their families. Our competitive total rewards benefits package, for eligible employees, include: Medical, Dental and Vision Plan Options Health and Financial Wellness Programs Employer Assistance Program (EAP) Company Paid and Voluntary Life/AD&D, Short-Term and Long-Term Disability Healthcare and Dependent Care Flexible Spending Accounts 401(k) Retirement Plan with Company Match 529 Education Savings Program Voluntary Legal Services, Identity Theft Protection, Pet Insurance and Employee Discounts, Rewards and Perks Paid Time Off (PTO) includes: 11 Holidays Exempt Employees are eligible for Unlimited PTO Non-Exempt Employees are eligible for 10 Vacation Days, 56 Hours of Health Pay, 2 Personal Days and 1 Cultural Day We are committed to providing you with the tools and resources you need to optimize your Health and Wellness.

At ImmunityBio, we are an equal opportunity employer dedicated to diversity in the workplace. Our policy is to provide equal employment opportunities to all qualified persons without regard to race, gender, color, disability, national origin, age, religion, union affiliation, sexual orientation, veteran status, citizenship, gender identity and/or expression, or other status protected by law.