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Fda Entry Level Jobs in Tennessee (NOW HIRING)

Tjoapack

Validation Writer

Clinton, TN · On-site

... FDA- and GMP-compliant documentation supporting primary and secondary pharmaceutical packaging operations as an entry level technical writer. Your primary responsibility is entry level Technical ...

Tjoapack

Validation Writer

Clinton, TN · On-site

... FDA- and GMP-compliant documentation supporting primary and secondary pharmaceutical packaging operations as an entry level technical writer. Your primary responsibility is entry level Technical ...

Vanderbilt Health

Cook

Nashville, TN · On-site

$13.50 - $18/hr

FDA/USDA Regulations (Novice): Possesses sufficient fundamental proficiency to successfully ... Provides guidance to entry level co-workers. Core Capabilities : Supporting Colleagues : Develops ...

Vanderbilt Health

Cook

Nashville, TN · On-site

$13.50 - $18/hr

FDA/USDA Regulations (Novice): Possesses sufficient fundamental proficiency to successfully ... Provides guidance to entry level co-workers. Core Capabilities : Supporting Colleagues : Develops ...

Vanderbilt Health

Food Service Associate

Nashville, TN · On-site

$13.50 - $17.75/hr

FDA/USDA Regulations (Novice): Possesses sufficient fundamental proficiency to successfully ... Provides guidance to entry level co-workers. Core Capabilities : Supporting Colleagues : Develops ...

Vanderbilt Health

Food Service Associate

Nashville, TN · On-site

$13.50 - $17.75/hr

FDA/USDA Regulations (Novice): Possesses sufficient fundamental proficiency to successfully ... Provides guidance to entry level co-workers. Core Capabilities : Supporting Colleagues : Develops ...

Vanderbilt Health

Cook

Nashville, TN · On-site

$13.50 - $18/hr

FDA/USDA Regulations (Novice): Possesses sufficient fundamental proficiency to successfully ... Provides guidance to entry level co-workers. Core Capabilities : Supporting Colleagues : Develops ...

Vanderbilt Health

Cook

Nashville, TN

$13.50 - $18/hr

FDA/USDA Regulations (Novice): Possesses sufficient fundamental proficiency to successfully ... Provides guidance to entry level co-workers. Core Capabilities : Supporting Colleagues : Develops ...

Care Access

Clinical Research Assistant

Memphis, TN · On-site

$19 - $33/hr

How This Role Makes a Difference The Clinical Research Assistant is an entry level clinical ... Maintain adherence to FDA regulations and ICH guidelines in all aspects of conducting clinical ...

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All JobsFda JobsFda Entry Level JobsFda Entry Level Jobs in Tennessee

Fda Entry Level information

See Tennessee salary details

$20.7K

$48.3K

$98.4K

How much do fda entry level jobs pay per year?

As of Jul 19, 2026, the average yearly pay for fda entry level in Tennessee is $48,304.00, according to ZipRecruiter salary data. Most workers in this role earn between $35,327.00 and $51,981.00 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 position at the FDA can be competitive due to high applicant volume and specific qualification requirements, such as relevant education and sometimes prior internship experience. Candidates often need strong academic backgrounds, knowledge of regulatory processes, and may be required to pass background checks and assessments. The hiring process can take several months, and relevant certifications or training can improve chances.

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.

What are the most commonly searched types of Fda jobs in Tennessee? The most popular types of Fda jobs in Tennessee are:
What are popular job titles related to Fda Entry Level jobs in Tennessee? For Fda Entry Level jobs in Tennessee, the most frequently searched job titles are:
What job categories do people searching Fda Entry Level jobs in Tennessee look for? The top searched job categories for Fda Entry Level jobs in Tennessee are:
What cities in Tennessee are hiring for Fda Entry Level jobs? Cities in Tennessee with the most Fda Entry Level job openings:
Fda Entry Level jobs near you
Infographic showing various Fda Entry Level job openings in Tennessee as of July 2026, with employment types broken down into 1% Locum Tenens, 86% Full Time, 10% Part Time, 1% Temporary, and 2% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $48,304 per year, or $23.2 per hour.

Validation Writer

Tjoapack

Clinton, TN • On-site

Full-time

Re-posted 11 days ago

Job description

Validation Writer

???? Clinton, TN | Full-time | Onsite
???? Department: Technical Services

About Tjoapack

Tjoapack is a global contract packaging organization (CPO) specializing in primary and secondary pharmaceutical packaging and supply chain management services. With more than 30 years of experience, we process millions of medicine packages every year for customers in over 45 countries worldwide.

Operating in Clinton, TN since 2021, Tjoapack is focused on delivering safe, compliant, and reliable packaging solutions—always with the patient at the center of our supply chain.

The Role

As a Validation Writer, you are a key member of the Technical Services team, responsible for developing FDA- and GMP-compliant documentation supporting primary and secondary pharmaceutical packaging operations as an entry level technical writer.

Your primary responsibility is entry level Technical Writing- authoring product-specific Master Batch Records (MBRs) executed during production, as well as equipment and component specific validation tests. You will also assist with the execution of qualification activities as needed, supporting new product introductions and validated packaging operations.

This role requires a strong understanding of packaging equipment and processes, along with the ability to clearly communicate technical concepts to diverse internal and external stakeholders.

One year of prior experience in a cGMP environment is required for consideration.

What You’ll Do

???? Process & Equipment Validation

  • Develop, author, and support execution of validation protocols including FAT, SAT, Engineering Studies (ES), IQ, OQ, and PQ.
  • Design equipment- and component-specific validation tests.
  • Assist with the execution of qualification activities as required.
  • Support Operational and Performance Qualifications for new products introduced to the facility.
  • Ensure equipment and processes meet GMP, FDA, and customer requirements.

???? Technical Documentation Development

  • Create and maintain product-specific Master Batch Records (MBRs).
  • Develop Master Setup Sheets and Work Instructions supporting validated processes.
  • Prepare Label Requests and ensure labeling accuracy and traceability.
  • Ensure documentation supports efficient, compliant, and validated production.

⚙️ Packaging & Component Evaluation

  • Perform technical evaluations of packaging components and processes.
  • Assess and document the impact of changes to packaging and serialization processes as they relate to validation and documentation requirements.

???? Project Support & Collaboration

  • Participate in cross-functional projects related to product introductions, validation, and process changes.
  • Collaborate with Engineering, Quality, Operations, and Production teams.
  • Support training of teams on new documentation, processes, or technologies as needed.

???? Continuous Improvement

  • Identify inefficiencies in validation or documentation processes.
  • Propose and implement process improvements.
  • Support or initiate RCAs, Change Controls, CAPAs, Risk Assessments, and Validation activities in accordance with Tjoapack procedures.
What We’re Looking For
  • One year of prior experience in a cGMP environment is required for consideration.
  • Experience in technical and/or validation writing.
  • Strong attention to detail and ability to follow regulatory requirements.
  • Excellent verbal and written communication skills.
  • Proficiency with Office 365 (Word, Excel) and Microsoft Teams.
  • Familiarity with manufacturing operations and production support.
  • Ability to manage multiple priorities and meet timelines in a regulated environment.
Why Join Us?
  • Play a critical role in supporting compliant, validated packaging operations.
  • Work cross-functionally with Engineering, Quality, and Production teams.
  • Gain exposure to new product introductions and pharmaceutical packaging validation.
  • Be part of a growing global organization with long-term stability.
  • Competitive compensation and benefits with opportunities for growth.
Pre-Employment Requirements ⚕️

All employment at Tjoapack is contingent upon successful completion of:

  • Background check
  • Drug screening
  • Physical examination
Apply Now

If you enjoy technical writing, validation work, and supporting regulated manufacturing environments, we’d love to hear from you.