Validation Engineer Jobs in North Carolina
Validation Engineer jobs in North Carolina are in steady demand, concentrated in the pharmaceutical and biotech manufacturing sector anchored along the Research Triangle, medical device companies near the Triad, and the growing life sciences corridor outside Charlotte. Most hiring happens in Raleigh, Durham, and the Research Triangle Park area, with additional volume in Greensboro and Charlotte, where employers like Biogen, Novo Nordisk, and Becton Dickinson maintain significant North Carolina operations. Computer systems validation, process validation for sterile manufacturing, and equipment qualification are the most in-demand specialties, with openings at every level from entry-level quality associate through senior validation lead. Find a role that fits below and apply directly.
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Showing 5 of 32+ Validation Engineer jobs
Validation Engineer / Specialist (Level II)
Raleigh, NC (Onsite) • Full-time • Travel required
About Us
Here at Performance Validation (PV) we have been providing Commissioning, Qualification, and Validation services to the life science industries for over 30 years! We are a 100% employee-owned company with teams in Indiana, Michigan, Illinois, Kansas, Washington, and North Carolina, and we support clients throughout the US and overseas. As an employer, PV is committed to providing growth opportunities to our employees through professional development, implementation of new services, and cultivation of new geographical areas.
About the Job
Performance Validation is seeking an experienced Validation Engineer/Specialist (Level II) to join our team in Raleigh, North Carolina. This is a role for someone who has moved past following existing protocols and is ready to build them — taking systems and equipment through the full commissioning, qualification, and validation lifecycle, from planning and requirements all the way to system acceptance and final summaries.
Much of the work happens where the answer is not written down yet. You will be trusted to think critically and develop testing criteria on your own when no relevant protocol exists, to propose and implement solutions as project work evolves, and to work directly with clients, vendors, management, and technical peers to reach consensus on design, testing, and approach.
It is also a step into leadership. Level II engineers lead tasks, perform independent validation and commissioning work, and mentor less experienced members of the team. You will be assigned to one or more project teams and report to a Project Leader, with your divisional home under a Division Director or Manager. At a 100% employee-owned company, the work you do here builds something you own a piece of due to stock ownership and biannual profit share.
What You Will Do
Knowledge
- Apply a well-developed knowledge of pharmaceutical industry government regulations, industry standards, and guidelines.
- Demonstrate an understanding of how those regulations and standards are incorporated into client quality systems — including CAPA, Change Control, and Validation.
- Develop commissioning, qualification, and validation documents for a system or piece of equipment from beginning to end — planning and requirements through system acceptance and final summaries.
- Develop and deliver technical presentations to peers and clients.
Development & Execution
- Implement the commissioning, qualification, or validation of a system or equipment end to end.
- Independently develop testing criteria in a creative environment where pre-existing protocol does not exist or is not relevant, written logically and clearly enough for others to follow.
- Propose and implement solutions relating to project work.
- Assess and develop the technical aspects of validation and commissioning activities — Master Plans, System Acceptance Final Reports, Risk Assessments, Audits, Gap Analyses, and Remediation Plans.
- Assist in the development or improvement of client quality systems.
- Develop and maintain equipment specification documents.
- Work directly with clients, vendors, management, and technical peers to gain consensus on design, testing, and approach.
Leadership
- Mentor less experienced resources.
- Lead tasks and perform independent validation and commissioning work, applying good project practices throughout.
Requirements You Will Need
Education
- Bachelor’s degree in Engineering, Management, Life Sciences, or another related technical field — or equivalent Nuclear Navy training.
Experience
- Two or more years of experience in the pharmaceutical or a comparable regulated life science industry.
- Depending on assignment, working knowledge of thermal mapping equipment, computer systems and software, or the principles of a specific scientific or technical discipline.
- Proficiency with Microsoft Word and Excel.
Skills You Will Bring
- Self-motivated, with a professional demeanor, real enthusiasm, and the ability to work independently.
- Flexible and dependable — willing to put in the extra time and effort to achieve a goal, and quick to offer help.
- Confident interaction with clients, contractors, management, and peers, representing the company and division professionally.
- Effective skills in developing, performing, evaluating, and troubleshooting operating systems and controls, or within a specific scientific or technical discipline.
- Excellent oral and written communication, high attention to detail, and the ability to manage several priorities at once.
What We Have to Offer
- Competitive base salary and biannual profit share
- Employee stock ownership program (ESOP) and 401(k) company match
- Medical, vision, and dental coverage
- Disability and life insurance
- Paid vacation and holidays
- Internal and external training opportunities
- Cellphone stipend
- Company-sponsored team building outings
- A collaborative work environment and genuine work/life balance
Additional Information
Please note that the salary range provided is a good faith estimate on the applicable range. The final salary offer will be determined after considering relevant factors, including a candidate’s qualifications and experience, where appropriate.
Position type: Full-time, exempt. This role reports to a Project Leader.
Location: This is an onsite position based in Raleigh, North Carolina.
Travel: Availability to travel is required.
Physical requirements: System walk downs require climbing stairs and ladders, maneuvering in and around tight spaces, and lifting moderate weight.
Qualified candidates must be legally authorized to be employed in the United States. Performance Validation does not anticipate providing sponsorship for employment visa status (e.g., H-1B or TN status) for this position.
Validation Engineer / Specialist (Level II)
Raleigh, NC (Onsite) • Full-time • Travel required
About Us
Here at Performance Validation (PV) we have been providing Commissioning, Qualification, and Validation services to the life science industries for over 30 years! We are a 100% employee-owned company with teams in Indiana, Michigan, Illinois, Kansas, Washington, and North Carolina, and we support clients throughout the US and overseas. As an employer, PV is committed to providing growth opportunities to our employees through professional development, implementation of new services, and cultivation of new geographical areas.
About the Job
Performance Validation is seeking an experienced Validation Engineer/Specialist (Level II) to join our team in Raleigh, North Carolina. This is a role for someone who has moved past following existing protocols and is ready to build them — taking systems and equipment through the full commissioning, qualification, and validation lifecycle, from planning and requirements all the way to system acceptance and final summaries.
Much of the work happens where the answer is not written down yet. You will be trusted to think critically and develop testing criteria on your own when no relevant protocol exists, to propose and implement solutions as project work evolves, and to work directly with clients, vendors, management, and technical peers to reach consensus on design, testing, and approach.
It is also a step into leadership. Level II engineers lead tasks, perform independent validation and commissioning work, and mentor less experienced members of the team. You will be assigned to one or more project teams and report to a Project Leader, with your divisional home under a Division Director or Manager. At a 100% employee-owned company, the work you do here builds something you own a piece of due to stock ownership and biannual profit share.
What You Will Do
Knowledge
- Apply a well-developed knowledge of pharmaceutical industry government regulations, industry standards, and guidelines.
- Demonstrate an understanding of how those regulations and standards are incorporated into client quality systems — including CAPA, Change Control, and Validation.
- Develop commissioning, qualification, and validation documents for a system or piece of equipment from beginning to end — planning and requirements through system acceptance and final summaries.
- Develop and deliver technical presentations to peers and clients.
Development & Execution
- Implement the commissioning, qualification, or validation of a system or equipment end to end.
- Independently develop testing criteria in a creative environment where pre-existing protocol does not exist or is not relevant, written logically and clearly enough for others to follow.
- Propose and implement solutions relating to project work.
- Assess and develop the technical aspects of validation and commissioning activities — Master Plans, System Acceptance Final Reports, Risk Assessments, Audits, Gap Analyses, and Remediation Plans.
- Assist in the development or improvement of client quality systems.
- Develop and maintain equipment specification documents.
- Work directly with clients, vendors, management, and technical peers to gain consensus on design, testing, and approach.
Leadership
- Mentor less experienced resources.
- Lead tasks and perform independent validation and commissioning work, applying good project practices throughout.
Requirements You Will Need
Education
- Bachelor’s degree in Engineering, Management, Life Sciences, or another related technical field — or equivalent Nuclear Navy training.
Experience
- Two or more years of experience in the pharmaceutical or a comparable regulated life science industry.
- Depending on assignment, working knowledge of thermal mapping equipment, computer systems and software, or the principles of a specific scientific or technical discipline.
- Proficiency with Microsoft Word and Excel.
Skills You Will Bring
- Self-motivated, with a professional demeanor, real enthusiasm, and the ability to work independently.
- Flexible and dependable — willing to put in the extra time and effort to achieve a goal, and quick to offer help.
- Confident interaction with clients, contractors, management, and peers, representing the company and division professionally.
- Effective skills in developing, performing, evaluating, and troubleshooting operating systems and controls, or within a specific scientific or technical discipline.
- Excellent oral and written communication, high attention to detail, and the ability to manage several priorities at once.
What We Have to Offer
- Competitive base salary and biannual profit share
- Employee stock ownership program (ESOP) and 401(k) company match
- Medical, vision, and dental coverage
- Disability and life insurance
- Paid vacation and holidays
- Internal and external training opportunities
- Cellphone stipend
- Company-sponsored team building outings
- A collaborative work environment and genuine work/life balance
Additional Information
Please note that the salary range provided is a good faith estimate on the applicable range. The final salary offer will be determined after considering relevant factors, including a candidate’s qualifications and experience, where appropriate.
Position type: Full-time, exempt. This role reports to a Project Leader.
Location: This is an onsite position based in Raleigh, North Carolina.
Travel: Availability to travel is required.
Physical requirements: System walk downs require climbing stairs and ladders, maneuvering in and around tight spaces, and lifting moderate weight.
Qualified candidates must be legally authorized to be employed in the United States. Performance Validation does not anticipate providing sponsorship for employment visa status (e.g., H-1B or TN status) for this position.
See All 32 Validation Engineer Jobs in North Carolina
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Find Validation Engineer JobsValidation Engineer Jobs by City in North Carolina
Where North Carolina roles are concentrated, by current openings.
Validation Engineer Job Market in North Carolina
A snapshot from current North Carolina openings, updated as new roles post.
Who's Hiring
Top Industries Hiring
- Consulting & Professional Services
- Science & Research
- Technology & Software
What North Carolina Employers Look For
The qualifications that appear most often in validation engineer jobs across North Carolina.
- Bachelor's degree in engineering, life sciences, or a closely related technical field
- Hands-on experience with IQ, OQ, and PQ protocols in a regulated manufacturing environment
- Working knowledge of FDA 21 CFR Part 11 and cGMP requirements for pharmaceutical or medical device facilities
- Proficiency writing and executing validation protocols, test scripts, and summary reports
- Familiarity with computerized systems validation and GAMP 5 guidelines
- Strong documentation practices and experience supporting audits or regulatory inspections
Validation Engineer Jobs in North Carolina: Frequently Asked Questions
How do you become a validation engineer in North Carolina?
Most validation engineer roles in North Carolina require a bachelor's degree in chemical, mechanical, electrical, or biomedical engineering, or in a life sciences field such as biochemistry or microbiology. No state-issued engineering license is required for this role, though a North Carolina Professional Engineer license can strengthen candidacy for senior positions. Employers in the Research Triangle and Triad actively recruit new graduates from NC State, UNC, and NC A&T who have cGMP coursework, laboratory experience, or internships in regulated industries.
Which companies hire validation engineers in North Carolina?
Employers hiring validation engineers in North Carolina right now include Thermo Fisher Scientific, Performance Validation, and CAI, based on current listings on Migrate Mate as of September 2026. North Carolina's dense concentration of pharmaceutical manufacturers, biotech firms, and contract development and manufacturing organizations in the Research Triangle Park area makes it one of the more active life sciences hiring markets on the East Coast.
Which North Carolina cities have the most validation engineer jobs?
Greenville, Raleigh, and Charlotte account for the most validation engineer openings in North Carolina. The Research Triangle area dominates because of its concentration of large pharmaceutical and biotech manufacturers in and around Research Triangle Park, while Greensboro and Charlotte draw additional volume from medical device companies and contract manufacturers that have established production facilities in the Piedmont region.
Are there remote validation engineer jobs in North Carolina?
Yes, but they're rare. Validation engineering is fundamentally a hands-on discipline requiring physical presence in manufacturing facilities, clean rooms, and labs to execute protocols and witness testing. About 18% of validation engineer openings tied to North Carolina are remote or hybrid as of September 2026, and those positions tend to focus on computer systems validation, documentation review, or project management rather than physical equipment qualification.
How can I get hired as a validation engineer in North Carolina with little or no experience?
The most realistic entry path is through a quality associate, manufacturing associate, or laboratory technician role at one of the large pharmaceutical or biotech manufacturers in the Research Triangle Park area, which regularly hire new graduates and train them into validation functions. Employers like Biogen and Novo Nordisk run structured development programs for junior quality and manufacturing talent. A strong foundation in GMP documentation, a relevant internship from NC State or UNC, and a working knowledge of FDA regulations will differentiate candidates without direct validation experience.
Where can I find and apply to validation engineer jobs in North Carolina?
You can find and apply to validation engineer jobs in North Carolina on Migrate Mate, which lists current openings across the state's pharmaceutical, biotech, and medical device sectors. Search the current listings, find roles that fit your experience and location, and apply directly to each one.
See All 32 Validation Engineer Jobs in North Carolina
Find roles in North Carolina that match your experience and apply in just a few clicks.
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