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Fda Entry Level Jobs (NOW HIRING)

Acro Service Corporation

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Quality Inspector

Salt Lake City, UT · On-site

$19/hr

Job Summary Entry-level Quality/Inspection role focused on performing mechanical, physical, and ... Exposure to medical device, regulated industry, or FDA standards preferred * Familiarity with ...

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FOOD FUSION NJ LLC

Quality Inspector

Bridgeton, NJ · On-site

$18 - $21/hr

Quality Technician Food Manufacturing | Entry-Level | Full-Time Department | Quality Assurance ... Support internal SQF audits and FDA/USDA inspection readiness by organizing records and ensuring ...

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FOOD FUSION NJ LLC

Quality Inspector

Bridgeton, NJ · On-site

$18 - $21/hr

Quality Technician Food Manufacturing | Entry-Level | Full-Time Department | Quality Assurance ... Support internal SQF audits and FDA/USDA inspection readiness by organizing records and ensuring ...

FOOD FUSION NJ LLC

Quality Inspector

Bridgeton, NJ · On-site

$18 - $21/hr

Quality Technician Food Manufacturing | Entry-Level | Full-Time Department | Quality Assurance ... Support internal SQF audits and FDA/USDA inspection readiness by organizing records and ensuring ...

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All JobsFda Entry Level Jobs

Fda Entry Level information

See salary details

$20.5K

$47.9K

$97.5K

How much do fda entry level jobs pay per year?

As of Jul 6, 2026, the average yearly pay for fda entry level in the United States is $47,856.00, according to ZipRecruiter salary data. Most workers in this role earn between $35,000.00 and $51,500.00 per year, depending on experience, location, and employer.

What qualifications do I need for FDA jobs?

For entry-level FDA jobs, candidates typically need a bachelor's degree in a relevant field such as biology, chemistry, or health sciences. Some positions may require knowledge of regulatory guidelines, good manufacturing practices, or quality assurance, and relevant certifications can be advantageous.

What are some typical responsibilities for someone in an FDA Entry Level position?

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 to thrive in the Fda Entry Level position, and why are they important?

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 is the starting salary for FDA?

The starting salary for an entry-level FDA employee typically ranges from $50,000 to $70,000 annually, depending on location, education, and experience. Entry-level roles often require a bachelor's degree and may include training on regulatory processes and compliance standards.

How difficult is it to get a job at the FDA?

Securing an entry-level FDA position can be competitive due to high standards for education, relevant experience, and sometimes specialized certifications. Candidates often need a strong academic background in science or healthcare, along with good interview skills and knowledge of regulatory processes. The hiring process typically involves multiple steps, including application reviews, assessments, and interviews, which can take several months.

How to start working for the FDA?

To start working as an FDA entry-level employee, candidates typically need a relevant bachelor's degree in fields like biology, chemistry, or health sciences, and may need to pass a background check. Applying through USAJOBS, the federal government's official job portal, is the standard process, and some positions require passing exams or obtaining specific certifications. Gaining experience through internships or related roles can also improve chances of employment.

What is a FDA Entry Level job?

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.

More about Fda Entry Level jobs
What cities are hiring for Fda Entry Level jobs? Cities with the most Fda Entry Level job openings:
What are the most commonly searched types of Fda jobs? The most popular types of Fda jobs are:
What states have the most Fda Entry Level jobs? States with the most job openings for Fda Entry Level jobs include:
What job categories do people searching Fda Entry Level jobs look for? The top searched job categories for Fda Entry Level jobs are:
Fda Entry Level jobs near you
Infographic showing various Fda Entry Level job openings in the United States as of June 2026, with employment types broken down into 40% Full Time, and 60% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $47,856 per year, or $23 per hour.
Quality Engineering Specialist (Entry Level)

Quality Engineering Specialist (Entry Level)

Kelly Services

Austin, TX

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 14 days ago

Job description

Quality Specialist, Entry Level 
Austin, Texas
Entry Level Contract Quality Specialist needed to review production records and assist with non-conformance management, incumbent will also support quality and training documentation. Technical and quality expertise within an FDA-regulated, ISO 13485 environment preferred, and emphasizes operational excellence and regulatory compliance.
This is an entry level position, client prefers a Contract to Hire (for speed to hire purposes). 
Summary:
Working collaboratively with Operations, Manufacturing, and Engineering teams, the Quality Inspector focus on supporting the transfer of manufacturing processes, quality documentation, and ensuring alignment with FDA and ISO standards.  
Key Responsibilities:
Ensure all quality inspection activities follow FDA QSR (21 CFR 820), ISO 13485, and relevant global medical device standards.
Review, update, and verify device history records, work instructions, validation protocols, and training certification documents for the new site.
Collaborate with R&D, Operations, Manufacturing, Regulatory, and Quality Assurance teams to facilitate the successful transfer of quality systems and training materials.
Update and maintain training documentation and assist with internal audits during the transition period.
Maintain meticulous records and use strong technical writing skills while managing risk throughout the process.
Assist with the review and approval of engineering change orders, nonconformances, and CAPAs as required.
Qualifications:
0-3 years experience in a fast-paced manufacturing environment with changing priorities.
0-3 years of quality assurance or quality inspection experience, or manufacturing documentation. Medical device, diagnostic, or biotechnology industry, and/or FDA familiarity preferred.
Associates or Bachelor's degree in life sciences (Biology, chemistry, biochemistry or similar) preferred.
Knowledge of FDA QSR (21 CFR 820), ISO 13485, quality documentation, design controls, validation, and CAPA processes.
Skilled in data analysis, risk management, deviation handling, technical writing, and audit support.
Excellent communication and teamwork skills; consistent attention to detail.
Commitment to operational and regulatory priorities over titles or manufacturing-only background.
About our Client:
Client is a global leader in diagnostic solutions, combining over 50 years of scientific and technological innovation to develop trusted diagnostic assays and instruments. Our products are used worldwide to improve patient care and clinical outcomes.
As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan. Click here for more information on benefits and perks that may be available to you as a member of the Kelly Talent Community.

Why Kelly® Engineering?

Your engineering skills are in demand, but how do you find the right fit? Easy. At Kelly Engineering, our team creates expert talent solutions to solve the world’s most critical challenges. We connect you with leading organizations where you can collaborate on innovative projects, work with cutting-edge technologies and accelerate your growth. Whether you prefer the variety and flexibility of short-term projects or are looking for a long-term opportunity, we’re here to guide you to the next step in your engineering career.

About Kelly

Work changes everything. And at Kelly, we’re obsessed with where it can take you. To us, it’s about more than simply accepting your next job opportunity. It’s the fuel that powers every next step of your life. It’s the ripple effect that changes and improves everything for your family, your community, and the world. Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life-just ask the 300,000 people we employ each year.
Kelly is committed to providing equal employment opportunities to all qualified employees and applicants regardless of race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center. Kelly complies with the requirements of California’s state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S.
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