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Computer Validation Jobs in North Carolina (NOW HIRING)

Staffingine LLC

Silicon Validation Engineer

Raleigh, NC · On-site

Silicon Validation Engineer Job Location: Raleigh NC Job Type: Contract * You will be responsible ... Bachelor's degree in electrical engineering, Computer Engineering, or a related field. * 7+ years ...

Oxford Biomedica

Validation Engineer III

Durham, NC · On-site

Analytical instruments, Computer Systems (as applicable to complex instruments and manufacturing equipment),Equipment, Utilities, and Facilities. * Development of Validation Plans and Validation Plan ...

Novartis

Validation Engineer III

Durham, NC · On-site

$183K/yr

Support computer systems validation activities for global systems and applications * Collaborate with cross-functional teams to support audits, inspections, and project execution Essential ...

Oxford Biomedica

Validation Engineer III

Durham, NC

Analytical instruments, Computer Systems (as applicable to complex instruments and manufacturing equipment),Equipment, Utilities, and Facilities. * Development of Validation Plans and Validation Plan ...

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Computer Validation information

See North Carolina salary details

$9

$49

$78

How much do computer validation jobs pay per hour?

As of Aug 7, 2026, the average hourly pay for computer validation in North Carolina is $49.36, according to ZipRecruiter salary data. Most workers in this role earn between $38.03 and $58.56 per hour, depending on experience, location, and employer.

Is computer validation a good field?

Computer validation is a specialized field within quality assurance and regulatory compliance, focusing on ensuring that computerized systems meet industry standards such as 21 CFR Part 11. It often requires knowledge of validation protocols, testing, and documentation, and can offer stable employment with opportunities for certification and skill development. The field is considered important in industries like pharmaceuticals and biotech, where system integrity and data accuracy are critical.

What is the difference between Computer Validation vs Quality Assurance Specialist?

AspectComputer ValidationQuality Assurance Specialist
Required CredentialsGxP, 21 CFR Part 11, validation certificationsISO standards, QA certifications, GxP knowledge
Work EnvironmentPharmaceutical, biotech, regulated industriesManufacturing, healthcare, regulated industries
Employer & Industry UsageRegulated industries requiring validated systemsEnsuring quality compliance across processes

Computer Validation focuses on verifying that computer systems meet regulatory requirements and function correctly, primarily in regulated industries. Quality Assurance Specialists oversee overall quality processes, ensuring compliance and standards across various operations. While both roles require knowledge of GxP and industry regulations, Computer Validation is more technical and system-specific, whereas QA Specialists have a broader scope in quality management.

What are popular job titles related to Computer Validation jobs in North Carolina? For Computer Validation jobs in North Carolina, the most frequently searched job titles are:
What job categories do people searching Computer Validation jobs in North Carolina look for? The top searched job categories for Computer Validation jobs in North Carolina are:
What cities in North Carolina are hiring for Computer Validation jobs? Cities in North Carolina with the most Computer Validation job openings:
Computer Validation jobs near you
Infographic showing various Computer Validation job openings in North Carolina as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 13% Part Time, 3% Contract, and 1% Nights. Highlights an 80% Physical, 1% Hybrid, and 19% Remote job distribution, with an average salary of $102,679 per year, or $49.4 per hour.

Validation Manager

Thermo Fisher Scientific

Greenville, NC

Full-time

Retirement

Re-posted 17 days ago

Thermo Fisher Scientific rating

7.7

Company rating: 7.7 out of 10

Based on 422 frontline employees who took The Breakroom Quiz

196th of 536 rated manufacturers

Job description

Work Schedule

First Shift (Days)

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)

Job Description

As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.
 

DESCRIPTION:
As a Validation Manager at Thermo Fisher Scientific, you will manage validation activities that ensure product quality and regulatory compliance. You'll develop validation strategy and oversee a team responsible for qualifying equipment, utilities, facilities, computer systems, and manufacturing processes. Working across functions, you'll ensure validation activities align with cGMP requirements while supporting new product introductions and technology transfers. This role offers the opportunity to make a meaningful impact by maintaining the validated state of systems that help produce therapeutics.
 

EDUCATION/EXPERIENCE:

  • Bachelor's degree in engineering, science, chemistry, biology or related technical discipline. Advanced Degree preferred

  • 6 - 8 years of experience in pharmaceutical/biotech manufacturing industry

  • 2+ years of experience with equipment, process, cleaning, and/or utility validation is required.

  • 3+ years of people management or team leadership experience

  • Demonstrated success managing complex validation projects and programs

  • Experience with validation master planning and change control systems

  • Experience participating in regulatory inspections and customer audits

  • Experience with smoke studies would be a plus

KNOWLEDGE, SKILLS, ABILITIES:

  • Strong knowledge of cGMP regulations, particularly FDA and EU requirements

  • Expertise in risk assessment methodologies and statistical analysis

  • Proficiency with quality systems and validation documentation

  • Excellent technical writing and documentation skills

  • Strong leadership, communication, and interpersonal abilities

  • Ability to influence and collaborate across functions and levels

  • Knowledge of lean/continuous improvement methodologies

  • Proficient with standard business software applications

NOTE: We are not able to offer relocation assistance or visa sponsorship for this role at this time. We offer competitive salary, an annual incentive bonus plan, 401K with company match up to 6%, tuition reimbursement and a range of other employee benefits! We foster an exciting company culture that encourages innovation, forward-thinking, and an outstanding career and development prospects. Come be a part of the team. We offer competitive salary, an annual incentive bonus plan, 401K with company match up to 6%, tuition reimbursement and a range of other employee benefits! We foster an exciting company culture that encourages innovation, forward-thinking, and an outstanding career and development prospects. Come be a part of the team!

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