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.
Find Validation Engineer JobsOverview
Showing 5 of 28+ Validation Engineer jobs
About Us:
BW Design Group is a fully integrated architecture, engineering, construction, system integration, and consulting firm committed to helping our clients realize their most critical goals from Strategy to Commercialization. As the only firm born from a manufacturing technology company to become an independent and fully integrated firm, we combine deep domain expertise in the manufacturing environment with an approach that is built to serve the dynamic needs of our clients. Rooted in our distinct culture of Truly Human Leadership, we cultivate the leaders who will define tomorrow and partner with our clients in the food & beverage, life sciences, industrial, and advanced technology industries to build the future of manufacturing and technology.Barry-Wehmiller is a diversified global supplier of engineering consulting and manufacturing technology for the packaging, corrugating, sheeting and paper-converting industries. By blending people-centric leadership with disciplined operational strategies and purpose-driven growth, Barry-Wehmiller has become a $3 billion organization with nearly 12,000 team members united by a common belief: to use the power of business to build a better world.
Job Description:
You will join one of our 45 offices in the US, be part of a committed team of over 1500 professionals, and work in teams and directly with our clients doing work that is shaping the world around us. You will be welcomed into a rapidly growing business and team and empowered to make an impact. You will be valued, cared for, and challenged on your path to becoming a world-class professional consultant and surrounded by leaders who are committed to creating an environment that enables you to realize your own success and fulfillment.
When you join Design Group as a Validation Engineer, you are joining a team that will challenge you and position you for growth. In this role, you will work with a team of industry experts to help the world’s leading companies solve their most difficult problems. You will join our Regulatory Compliance Practice and partner with seasoned leaders, technical specialists, and subject matter experts to deliver the highest quality solutions to our clients with consistency and accuracy.
What You’ll Do
You'll work individually and in teams to support capital projects and implement solutions for our clients. Together, you will help our clients make critical changes to improve their performance and realize their most important goals.
Responsible for developing and executing a variety of validation and FDA compliance related documents/protocols for pharmaceutical equipment. This person will travel to top clients across the country to assist in the design of manufacturing processes, help manage projects, develop facilities, and impact the world by conducting themselves with integrity in pursuit of individual and enterprise goals. This role will challenge you to be a passionate and successful business family member all while expanding your technical abilities.
FAT, SAT, IQ and OQ documentation development and execution on Automated Systems in the pharmaceutical industry
Assist in the development and execution of QMS procedures, ICH Q1 (Stability Protocols / Reports), CFR 21 Part 211, CFR 21 Part 820, ICH Q8, ICH Q9, and ICH Q10
Work with teams to perform investigations and troubleshoot issues related to validation
Prepare written validation reports
Make an impact day-to-day with your skills and expertise, strengthening that relationship with our clients and team
What You’ll Bring
Candidates need to possess good communication and interpersonal skills, flexibility with tasks and the ability to interact with all levels of management, clients, and vendors
Minimum of 2 years project experience with validation of automation, packaging, utilities and/or facilities is desired
Minimum of 1 year project experience in the pharmaceutical, life science, or biotech environments is a plus
Strong technical writing and oral communications
Strong computer skills (Microsoft Office, Microsoft Project, & AutoCAD)
Willing and able to travel as necessary for project requirements to include but not be limited to project installation and start-up activities, client meetings, company sponsored meetings, trainings, industry related seminars, forums, or conventions, etc.
B.S. in Bioengineering, Biomedical Engineering, Chemical Engineering, or related technical degree.
Our culture and commitment to our people is what sets us apart. We foster an environment of mutual respect, integrity, and unconditional interest in the individual and collective success of our professionals. Our model and entrepreneurial mindset offer a rewarding, challenging, and highly flexible path. As a Validation Engineer, you will build a meaningful and fulfilling career with the support of professional development resources and mentorships including our First Year Experience program, Individual Development Plans, and Career Path resources and tools. You will be surrounded by exceptional talent who will support your development as both a world-class engineer and a highly effective leader.
#LI-EPS
At Barry-Wehmiller we recognize that people come with a wealth of experience and talent beyond just the technical requirements of a job. If your experience is close to what you see listed here, please still consider applying. We know that our differences often can bring about innovation, excellence and meaningful work—therefore, people from all backgrounds are encouraged to apply to our positions. Please let us know if you require reasonable accommodations during the interview process.
Barry-Wehmiller is an equal opportunity employer. M/F/D/V This organization uses E-Verify.Applicants may be subject to pre-employment screening which may include drug screening, reference checks, employment verifications, background screening and/or skills assessments.
Company:
Design GroupAbout Us:
BW Design Group is a fully integrated architecture, engineering, construction, system integration, and consulting firm committed to helping our clients realize their most critical goals from Strategy to Commercialization. As the only firm born from a manufacturing technology company to become an independent and fully integrated firm, we combine deep domain expertise in the manufacturing environment with an approach that is built to serve the dynamic needs of our clients. Rooted in our distinct culture of Truly Human Leadership, we cultivate the leaders who will define tomorrow and partner with our clients in the food & beverage, life sciences, industrial, and advanced technology industries to build the future of manufacturing and technology.Barry-Wehmiller is a diversified global supplier of engineering consulting and manufacturing technology for the packaging, corrugating, sheeting and paper-converting industries. By blending people-centric leadership with disciplined operational strategies and purpose-driven growth, Barry-Wehmiller has become a $3 billion organization with nearly 12,000 team members united by a common belief: to use the power of business to build a better world.
Job Description:
You will join one of our 45 offices in the US, be part of a committed team of over 1500 professionals, and work in teams and directly with our clients doing work that is shaping the world around us. You will be welcomed into a rapidly growing business and team and empowered to make an impact. You will be valued, cared for, and challenged on your path to becoming a world-class professional consultant and surrounded by leaders who are committed to creating an environment that enables you to realize your own success and fulfillment.
When you join Design Group as a Validation Engineer, you are joining a team that will challenge you and position you for growth. In this role, you will work with a team of industry experts to help the world’s leading companies solve their most difficult problems. You will join our Regulatory Compliance Practice and partner with seasoned leaders, technical specialists, and subject matter experts to deliver the highest quality solutions to our clients with consistency and accuracy.
What You’ll Do
You'll work individually and in teams to support capital projects and implement solutions for our clients. Together, you will help our clients make critical changes to improve their performance and realize their most important goals.
Responsible for developing and executing a variety of validation and FDA compliance related documents/protocols for pharmaceutical equipment. This person will travel to top clients across the country to assist in the design of manufacturing processes, help manage projects, develop facilities, and impact the world by conducting themselves with integrity in pursuit of individual and enterprise goals. This role will challenge you to be a passionate and successful business family member all while expanding your technical abilities.
FAT, SAT, IQ and OQ documentation development and execution on Automated Systems in the pharmaceutical industry
Assist in the development and execution of QMS procedures, ICH Q1 (Stability Protocols / Reports), CFR 21 Part 211, CFR 21 Part 820, ICH Q8, ICH Q9, and ICH Q10
Work with teams to perform investigations and troubleshoot issues related to validation
Prepare written validation reports
Make an impact day-to-day with your skills and expertise, strengthening that relationship with our clients and team
What You’ll Bring
Candidates need to possess good communication and interpersonal skills, flexibility with tasks and the ability to interact with all levels of management, clients, and vendors
Minimum of 2 years project experience with validation of automation, packaging, utilities and/or facilities is desired
Minimum of 1 year project experience in the pharmaceutical, life science, or biotech environments is a plus
Strong technical writing and oral communications
Strong computer skills (Microsoft Office, Microsoft Project, & AutoCAD)
Willing and able to travel as necessary for project requirements to include but not be limited to project installation and start-up activities, client meetings, company sponsored meetings, trainings, industry related seminars, forums, or conventions, etc.
B.S. in Bioengineering, Biomedical Engineering, Chemical Engineering, or related technical degree.
Our culture and commitment to our people is what sets us apart. We foster an environment of mutual respect, integrity, and unconditional interest in the individual and collective success of our professionals. Our model and entrepreneurial mindset offer a rewarding, challenging, and highly flexible path. As a Validation Engineer, you will build a meaningful and fulfilling career with the support of professional development resources and mentorships including our First Year Experience program, Individual Development Plans, and Career Path resources and tools. You will be surrounded by exceptional talent who will support your development as both a world-class engineer and a highly effective leader.
#LI-EPS
At Barry-Wehmiller we recognize that people come with a wealth of experience and talent beyond just the technical requirements of a job. If your experience is close to what you see listed here, please still consider applying. We know that our differences often can bring about innovation, excellence and meaningful work—therefore, people from all backgrounds are encouraged to apply to our positions. Please let us know if you require reasonable accommodations during the interview process.
Barry-Wehmiller is an equal opportunity employer. M/F/D/V This organization uses E-Verify.Applicants may be subject to pre-employment screening which may include drug screening, reference checks, employment verifications, background screening and/or skills assessments.
Company:
Design GroupSee All 28 Validation Engineer Jobs in North Carolina
Find roles in North Carolina that match your experience and apply in just a few clicks.
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
- Manufacturing
- Technology & Software
- Electronics & Hardware
- Biotechnology & Pharmaceuticals
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, CAI, and Verista, based on current listings on Migrate Mate as of August 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, Charlotte, and Durham 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 0% of validation engineer openings tied to North Carolina are remote or hybrid as of August 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 28 Validation Engineer Jobs in North Carolina
Find roles in North Carolina that match your experience and apply in just a few clicks.
Find Validation Engineer Jobs