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Validation Engineer Entry Level Jobs in North Carolina

Entry-Level Project Engineer

Cary, NC · On-site

$62K - $82K/yr

ENTRY LEVEL PROJECT ENGINEER (EI) Giles Flythe Engineers, Inc. is looking for an entry-level ... Valid Driver's license with a good driving record. ABOUT GILES FLYTHE ENGINEERS (GFE): Giles Flythe ...

Entry-Level Project Engineer

Cary, NC · On-site

$62K - $82K/yr

ENTRY LEVEL PROJECT ENGINEER (EI)Giles Flythe Engineers, Inc. is looking for an entry-level ... Valid Driver's license with a good driving record.ABOUT GILES FLYTHE ENGINEERS (GFE):Giles Flythe ...

Dewberry's Raleigh, NC office is currently seeking an Entry Level Site/Civil Engineer to support ... Dewberry only compensates job placement recruiters that have a valid Dewberry-approved written ...

Dewberry's Raleigh, NC office is currently seeking an Entry Level Site/Civil Engineer to support ... Dewberry only compensates job placement recruiters that have a valid Dewberry-approved written ...

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Validation Engineer Entry Level information

What is a validation engineer entry level?

An Entry-Level Validation Engineer is responsible for testing and verifying that products, systems, or processes meet required standards and specifications. They work in industries like pharmaceuticals, manufacturing, and software, ensuring compliance with regulations and quality standards. Their tasks may include writing test protocols, analyzing data, and troubleshooting issues. This role requires attention to detail, problem-solving skills, and knowledge of engineering principles. Typically, they work under supervision but gain experience to take on more complex validation tasks over time.

What are the typical daily responsibilities of a validation engineer entry level?

As an Entry Level Validation Engineer, your daily tasks often include executing validation protocols, documenting test results, and assisting with equipment or process qualification under supervision. You'll collaborate closely with senior engineers, quality assurance teams, and production staff to ensure systems meet regulatory and company standards. Troubleshooting, process improvement, and maintaining accurate records are also common parts of the role. This position is a great opportunity to develop technical expertise and gain practical experience in a regulated industry, setting the foundation for future career advancement.

What are the key skills and qualifications needed to thrive in a validation engineer entry level position?

To thrive as a Validation Engineer Entry Level, you need a solid background in engineering or the life sciences, attention to detail, and a basic understanding of validation protocols and regulatory standards. Familiarity with technical tools such as data logging software, validation documentation, and quality management systems like ISO or GMP is highly valuable. Strong analytical thinking, problem-solving, and effective communication are crucial soft skills for collaborating with multidisciplinary teams and presenting findings. These abilities ensure accuracy, compliance, and effective teamwork in delivering reliable processes and products in regulated industries.

What are the most commonly searched types of Validation Engineer jobs in North Carolina?

The most popular types of Validation Engineer jobs in North Carolina are:

What are popular job titles related to Validation Engineer Entry Level jobs in North Carolina?

For Validation Engineer Entry Level jobs in North Carolina, the most frequently searched job titles are:

What job categories do people searching Validation Engineer Entry Level jobs in North Carolina look for?

The top searched job categories for Validation Engineer Entry Level jobs in North Carolina are:

What cities in North Carolina are hiring for Validation Engineer Entry Level jobs?

Cities in North Carolina with the most Validation Engineer Entry Level job openings:

Infographic showing various Validation Engineer Entry Level job openings in North Carolina as of August 2026, with employment types broken down into 95% Full Time, 2% Part Time, and 3% Contract. Highlights an 85% Physical, 5% Hybrid, and 10% Remote job distribution.

Engineer II, Validation - AVI

Greenville, NC • On-site


Thermo Fisher Scientific
Biotechnology Research and Development • 10K+ employees

7.8

Company rating: 7.8 out of 10

Based on 429 frontline employees who took The Breakroom Quiz

170th of 544 rated manufacturers

People enjoy working here

Good employer

Recommended by students


Full-time

Re-posted 14 hours ago


Job description

Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Office
Job Description
Discover Impactful Work:
As part of the Thermo Fisher Scientific team, you'll do meaningful work that makes a positive impact on a global scale. Join colleagues who bring our Mission to life every day-enabling customers to make the world healthier, cleaner, and safer.
Join our growing validation team supporting Automatic Visual Inspection (AVI) operations, a critical and expanding function within sterile pharmaceutical manufacturing. With new lines being added-including auto-injector technology-this role offers hands-on experience in one of the most in-demand areas of the industry.
This is an entry-level opportunity designed for growth, where you'll gain valuable, highly marketable experience in sterile manufacturing validation.
A Day in the Life:
This role offers a balance of technical documentation and hands-on execution:
  • ~60% desk-based: writing validation protocols, data analysis, reporting, and documentation
  • ~40% on the production floor: executing validation activities alongside team members
  • Partner with experienced engineers for hands-on training and execution
  • Participate in data calculations, evaluations, and summary reports
  • Gradually interface with clients and become a point of contact
  • Work directly with commercial manufacturing equipment in sterile/inspection environments

What to Expect:
  • Structured onboarding with SOP training and hands-on mentorship
  • Direct exposure to AVI and sterile pharmaceutical processes
  • Career growth within a rapidly expanding function (AVI + auto-injector lines)
  • Collaborative team environment (team of ~4 engineers)

Keys to Success:
Education & Experience:
  • Bachelor's degree in Engineering, Life Sciences, Chemistry, or related field
  • 0-2+ years of experience in validation or regulated/GMP environment preferred
Required Skills & Experience:
  • Strong technical writing and documentation skills
  • High attention to detail and quality-focused mindset
  • Comfort working around large-scale manufacturing equipment
  • Ability to learn quickly in a hands-on environment
  • Exposure to pharmaceutical manufacturing-especially sterile/aseptic environments-is strongly preferred and highly valued

Additional Requirements:
  • Knowledge of cGMP and regulated environments preferred
  • Familiarity with IQ/OQ/PQ concepts a plus
  • Ability to work onsite in Greenville, NC (Monday-Friday, standard hours)
  • Strong communication and teamwork skills

Why Join Us:
  • Entry point into high-demand sterile validation engineering
  • Hands-on learning with experienced mentors
  • Exposure to cutting-edge pharmaceutical technologies (AVI & auto-injectors)
  • Clear career progression into advanced validation roles


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