Validation Specialist Jobs in North Carolina
Validation Specialist jobs in North Carolina are in steady demand, concentrated in the state's pharmaceutical manufacturing, biotechnology, medical device, and life sciences sectors, with openings at every level from entry-level quality associates through senior validation engineers. The heaviest hiring activity is in the Research Triangle area, Charlotte, and Wilmington, where employers like Novo Nordisk, Pfizer, and Thermo Fisher Scientific maintain large operations. Computer system validation, process validation, and equipment qualification are the specialties appearing most consistently across North Carolina postings. Find a role that fits below and apply directly.
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Showing 5 of 9+ Validation Specialist jobs
Quality Control Validation Area Specialist I
- Leading pay and annual performance bonus for all positions
- All employees enjoy generous paid time off including 14 paid holidays
- Health Insurance, Dental Insurance, Vision Insurance – effective day one
- Guaranteed 8% 401K contribution plus individual company match option
- Family Focused Benefits including 14 weeks paid parental & 6 weeks paid family medical leave
- Free access to Novo Nordisk-marketed pharmaceutical products
- Tuition Assistance
- Life & Disability Insurance
- Employee Referral Awards
- Accuracy & compliance of validation & equipment records
- Validation responsible for QC equipment & instrumentation
- Identify & handle deviations per proper appropriate procedures
- Maintain good standing with stakeholders through engagement & positive cooperation
- Perform & oversee change control activities for QC equipment & systems
- Follow all safety and environmental requirements in the performance of duties
- Other accountabilities, as assigned
- Bachelor’s Degree in Life Sciences, Chemistry, Engineering or a relevant field of study from an accredited university required
- May consider Associate's Degree in Life Sciences, Chemistry, Engineering or a relevant field of study from an accredited university with a minimum of four (4) years of instrument, laboratory validation, or engineering experience in the pharmaceutical industry or related field required
- Minimum of two (2) years of instrument, laboratory validation, or engineering experience in the pharmaceutical industry or related field required
- Experience in writing & executing validation protocols preferred
- Experience in managing projects preferred
- Experience with electronic validation systems (TIMS) and SAP PM and QM module a plus
- Working knowledge of GMPs required
- Ability to act as project manager driving & implementing equipment projects required
- Demonstrated ability to write & present technical/scientific documents & reports preferred
- Understanding of QC equipment/systems, end user functionality & life-cycle management a plus
We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.
Quality Control Validation Area Specialist I
- Leading pay and annual performance bonus for all positions
- All employees enjoy generous paid time off including 14 paid holidays
- Health Insurance, Dental Insurance, Vision Insurance – effective day one
- Guaranteed 8% 401K contribution plus individual company match option
- Family Focused Benefits including 14 weeks paid parental & 6 weeks paid family medical leave
- Free access to Novo Nordisk-marketed pharmaceutical products
- Tuition Assistance
- Life & Disability Insurance
- Employee Referral Awards
- Accuracy & compliance of validation & equipment records
- Validation responsible for QC equipment & instrumentation
- Identify & handle deviations per proper appropriate procedures
- Maintain good standing with stakeholders through engagement & positive cooperation
- Perform & oversee change control activities for QC equipment & systems
- Follow all safety and environmental requirements in the performance of duties
- Other accountabilities, as assigned
- Bachelor’s Degree in Life Sciences, Chemistry, Engineering or a relevant field of study from an accredited university required
- May consider Associate's Degree in Life Sciences, Chemistry, Engineering or a relevant field of study from an accredited university with a minimum of four (4) years of instrument, laboratory validation, or engineering experience in the pharmaceutical industry or related field required
- Minimum of two (2) years of instrument, laboratory validation, or engineering experience in the pharmaceutical industry or related field required
- Experience in writing & executing validation protocols preferred
- Experience in managing projects preferred
- Experience with electronic validation systems (TIMS) and SAP PM and QM module a plus
- Working knowledge of GMPs required
- Ability to act as project manager driving & implementing equipment projects required
- Demonstrated ability to write & present technical/scientific documents & reports preferred
- Understanding of QC equipment/systems, end user functionality & life-cycle management a plus
We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.
See All 9 Validation Specialist Jobs in North Carolina
Find roles in North Carolina that match your experience and apply in just a few clicks.
Find Validation Specialist JobsValidation Specialist Jobs by City in North Carolina
Where North Carolina roles are concentrated, by current openings.
Validation Specialist Job Market in North Carolina
A snapshot from current North Carolina openings, updated as new roles post.
Who's Hiring
Top Industries Hiring
- Science & Research
- Biotechnology & Pharmaceuticals
- Consulting & Professional Services
What North Carolina Employers Look For
The qualifications that appear most often in validation specialist jobs across North Carolina.
- Bachelor's degree in engineering, life sciences, chemistry, or a related field
- Experience with FDA 21 CFR Part 11 compliance and GMP validation protocols
- Proficiency in writing validation plans, protocols, and summary reports
- Familiarity with GAMP 5 guidelines and computer system validation practices
- Experience executing IQ, OQ, and PQ validation activities in regulated environments
- Strong documentation skills and attention to detail for cGMP-regulated facilities
Validation Specialist Jobs in North Carolina: Frequently Asked Questions
How do you become a validation specialist in North Carolina?
Most validation specialist roles in North Carolina require a bachelor's degree in engineering, biology, chemistry, or a related life sciences field. There is no state-issued license for this role, but employers in North Carolina's pharmaceutical and biotech sectors expect familiarity with FDA regulations and GMP practices. Earning credentials like the ASQ Certified Quality Engineer or completing training in GAMP 5 and computer system validation strengthens your candidacy considerably for Research Triangle and Charlotte-area openings.
How much do validation specialists make in North Carolina?
Validation specialists in North Carolina earn a median of about $99,310 a year, based on May 2025 Bureau of Labor Statistics wage data, ranging from around $68,930 for the lowest 10% to over $139,110 for the top 10%. Pay rises with experience, specialty, and employer.
Which companies hire validation specialists in North Carolina?
Employers hiring validation specialists in North Carolina right now include Novo Nordisk, Katalyst Healthcares & Life Sciences, and CSL Plasma, based on current listings on Migrate Mate as of August 2026. North Carolina's concentration of pharmaceutical manufacturers, contract research organizations, and medical device companies along the Research Triangle corridor means demand for validation specialists remains consistent throughout the year.
Which North Carolina cities have the most validation specialist jobs?
The cities with the most validation specialist openings in North Carolina are Clayton, Durham, and Marion. The Research Triangle area leads because of its dense cluster of pharmaceutical manufacturers, biotech firms, and contract research organizations, while Charlotte draws openings from medical device companies and regulated manufacturing facilities, and Wilmington contributes through its growing life sciences presence anchored by large pharmaceutical production sites.
Are there remote validation specialist jobs in North Carolina?
Yes, but they're rare. Validation specialist work is largely hands-on, requiring physical presence for equipment qualification, process validation runs, and on-site documentation in GMP facilities. About 100% of validation specialist openings tied to North Carolina are remote or hybrid as of August 2026, and those tend to be limited to computer system validation or documentation-heavy compliance roles that do not require lab or manufacturing floor access.
How can I get hired as a validation specialist in North Carolina with little or no experience?
The most realistic entry path is a quality associate or quality technician role at one of North Carolina's pharmaceutical or contract manufacturing organizations, where you can gain hands-on GMP and documentation experience before moving into validation. Large Research Triangle employers like Pfizer and Novo Nordisk run structured new-graduate programs, and contract research organizations often hire candidates with relevant internship experience. An ASQ certification or coursework in regulatory affairs gives entry-level candidates a concrete edge in a competitive field.
Where can I find and apply to validation specialist jobs in North Carolina?
You can find and apply to validation specialist jobs in North Carolina on Migrate Mate, which lists current openings across the state's pharmaceutical, biotech, and medical device sectors. Find roles that fit your experience and apply directly to the ones that match.
See All 9 Validation Specialist Jobs in North Carolina
Find roles in North Carolina that match your experience and apply in just a few clicks.
Find Validation Specialist Jobs