Quality Inspector Jobs in North Carolina
Quality Inspector jobs in North Carolina are consistently active, with demand concentrated in aerospace and defense manufacturing, automotive components, pharmaceuticals, and industrial equipment production from entry-level inspection roles through senior quality engineer positions. The heaviest hiring is in Charlotte, Greensboro, and the Research Triangle, where companies like Caterpillar, Honeywell, and Danaher maintain significant manufacturing and operations footprints. The most in-demand specialties include CMM programming and dimensional inspection, ISO and AS9100 audit readiness, and incoming and in-process inspection for regulated industries. Find a role that fits below and apply directly.
Find Quality Inspector JobsOverview
Showing 5 of 94+ Quality Inspector jobs
Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions.
This position is on-site only at our Clayton, NC Facility.
Hours: 2nd Shift (10 hour) Monday - Thursday 1:30pm - 12:00am
Summary:
Quality Assurance Inspectors work with manufacturing operations during the production process, by approving the raw materials and associated documentation for incoming plasma shipments from donor collection centers and the in-process production batches (Production Units - PUs) at the Plasma Logistics Center (PLC). Quality Assurance Inspectors identify and document deviations of both materials and the manufacturing process and ensure these deviations are corrected to ensure a better finished product for prospective customers.
Primary Responsibilities:
- Approves incoming plasma shipment documentation and raw materials by confirming specifications, rejects and returns unacceptable materials as directed by QA Supervisor.
- Generates and documents non-conformance of plasma units or procedures associated with plasma shipments, PUs or final plasma lots.
- Approves PUs by confirming customer and regulatory specifications and communicating required adjustments to the QA Supervisor.
- Responsible for inspecting final outgoing plasma lot shipments to ensure all pallets are properly packaged and loaded for sales and distribution.
- Investigates and reports in-process/final product and processes that do not meet quality specifications and document in a deviation report.
- Participates in the writing or revision of policies and standard operating procedures related to Source Plasma and quality systems at GPLC.
- Executes repetitive functions with strict adherence to procedures and maintains record accountability.
- Documents approval activities in the organizations computer system.
Knowledge, Skills, and Abilities:
- Good communication skills with the ability to express ideas with clarity and thoroughness in both verbal and written communications.
- Proactive, results oriented with a strong attention to detail.
- Strong interpersonal skills to interface with manufacturing operators and various levels of management as well as with support and service departments.
- Ability to work in a team-oriented environment and follow safety guidelines.
- Must be computer literate with experience in the use of Microsoft applications.
- Able to perform basic arithmetic functions including addition, subtraction, multiplication, division and using decimals.
Education and Experience:
- High School diploma or GED.
- Typically requires a minimum of 1 year of Quality Assurance related experience and 2 years working in pharmaceuticals. Experience in the pharmaceutical, plasma/blood banking or medical device industry is ideal and working knowledge of cGMP helpful.
- Depending on the area of assignment, directly related experience or a combination of directly related education and experience and/or competencies may be considered in place of the stated requirements. Example: If a job level typically requires an Associate’s degree plus 2 years of experience, an equivalent could include 4 years of experience or a Bachelor's degree.
This position is eligible to participate in up to 5% of the company bonus pool. We offer a wide variety of benefits including, but not limited to: Medical, Dental, Vision, PTO, up to 5% 401(K) match and tuition reimbursement. Final compensation packages will ultimately depend on education, experience, skillset, knowledge, where the role is performed, internal equity and market data. We are committed to offering our employees opportunities for professional growth and career progression. Grifols is a global healthcare organization with employees in 30 countries focused on patient health and providing impactful results. Since our humble beginnings in 1909, Grifols has been a family company that prides itself on its family-like culture. Our company has more than tripled over the last 10 years, and you can grow with us!
Third Party Agency and Recruiter Notice:
Agencies that present a candidate to Grifols must have an active, nonexpired, Grifols Agency Master Services Agreement with the Grifols Talent Acquisition Department. Additionally, agencies may only submit candidates to positions that they have been engaged to work on by a Grifols Recruiter. All resumes must be sent to a Grifols Recruiter under these terms or they will be considered a Grifols candidate.
Grifols provides equal employment opportunities to applicants and employees without regard to race; color; sex; gender identity; sexual orientation; religious practices and observances; national origin; pregnancy, childbirth, or related medical conditions; status as a protected veteran or spouse/family member of a protected veteran; or disability. We will consider for employment all qualified applicants in a manner consistent with the requirements of all applicable laws.
Location: NORTH AMERICA : USA : NC-Clayton:USNC0002 - Clayton
Learn more about Grifols
Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions.
This position is on-site only at our Clayton, NC Facility.
Hours: 2nd Shift (10 hour) Monday - Thursday 1:30pm - 12:00am
Summary:
Quality Assurance Inspectors work with manufacturing operations during the production process, by approving the raw materials and associated documentation for incoming plasma shipments from donor collection centers and the in-process production batches (Production Units - PUs) at the Plasma Logistics Center (PLC). Quality Assurance Inspectors identify and document deviations of both materials and the manufacturing process and ensure these deviations are corrected to ensure a better finished product for prospective customers.
Primary Responsibilities:
- Approves incoming plasma shipment documentation and raw materials by confirming specifications, rejects and returns unacceptable materials as directed by QA Supervisor.
- Generates and documents non-conformance of plasma units or procedures associated with plasma shipments, PUs or final plasma lots.
- Approves PUs by confirming customer and regulatory specifications and communicating required adjustments to the QA Supervisor.
- Responsible for inspecting final outgoing plasma lot shipments to ensure all pallets are properly packaged and loaded for sales and distribution.
- Investigates and reports in-process/final product and processes that do not meet quality specifications and document in a deviation report.
- Participates in the writing or revision of policies and standard operating procedures related to Source Plasma and quality systems at GPLC.
- Executes repetitive functions with strict adherence to procedures and maintains record accountability.
- Documents approval activities in the organizations computer system.
Knowledge, Skills, and Abilities:
- Good communication skills with the ability to express ideas with clarity and thoroughness in both verbal and written communications.
- Proactive, results oriented with a strong attention to detail.
- Strong interpersonal skills to interface with manufacturing operators and various levels of management as well as with support and service departments.
- Ability to work in a team-oriented environment and follow safety guidelines.
- Must be computer literate with experience in the use of Microsoft applications.
- Able to perform basic arithmetic functions including addition, subtraction, multiplication, division and using decimals.
Education and Experience:
- High School diploma or GED.
- Typically requires a minimum of 1 year of Quality Assurance related experience and 2 years working in pharmaceuticals. Experience in the pharmaceutical, plasma/blood banking or medical device industry is ideal and working knowledge of cGMP helpful.
- Depending on the area of assignment, directly related experience or a combination of directly related education and experience and/or competencies may be considered in place of the stated requirements. Example: If a job level typically requires an Associate’s degree plus 2 years of experience, an equivalent could include 4 years of experience or a Bachelor's degree.
This position is eligible to participate in up to 5% of the company bonus pool. We offer a wide variety of benefits including, but not limited to: Medical, Dental, Vision, PTO, up to 5% 401(K) match and tuition reimbursement. Final compensation packages will ultimately depend on education, experience, skillset, knowledge, where the role is performed, internal equity and market data. We are committed to offering our employees opportunities for professional growth and career progression. Grifols is a global healthcare organization with employees in 30 countries focused on patient health and providing impactful results. Since our humble beginnings in 1909, Grifols has been a family company that prides itself on its family-like culture. Our company has more than tripled over the last 10 years, and you can grow with us!
Third Party Agency and Recruiter Notice:
Agencies that present a candidate to Grifols must have an active, nonexpired, Grifols Agency Master Services Agreement with the Grifols Talent Acquisition Department. Additionally, agencies may only submit candidates to positions that they have been engaged to work on by a Grifols Recruiter. All resumes must be sent to a Grifols Recruiter under these terms or they will be considered a Grifols candidate.
Grifols provides equal employment opportunities to applicants and employees without regard to race; color; sex; gender identity; sexual orientation; religious practices and observances; national origin; pregnancy, childbirth, or related medical conditions; status as a protected veteran or spouse/family member of a protected veteran; or disability. We will consider for employment all qualified applicants in a manner consistent with the requirements of all applicable laws.
Location: NORTH AMERICA : USA : NC-Clayton:USNC0002 - Clayton
Learn more about Grifols
See All 94 Quality Inspector Jobs in North Carolina
Find roles in North Carolina that match your experience and apply in just a few clicks.
Find Quality Inspector JobsQuality Inspector Jobs by City in North Carolina
Where North Carolina roles are concentrated, by current openings.
Quality Inspector Job Market in North Carolina
A snapshot from current North Carolina openings, updated as new roles post.
Who's Hiring
Top Industries Hiring
- Manufacturing
- Technology & Software
- Electronics & Hardware
- Construction & Real Estate
What North Carolina Employers Look For
The qualifications that appear most often in quality inspector jobs across North Carolina.
- High school diploma or GED with relevant manufacturing or inspection experience required
- Proficiency reading and interpreting engineering drawings, blueprints, and GD&T symbols
- Experience with measuring instruments including calipers, micrometers, and gauges
- Familiarity with quality management systems such as ISO 9001 or AS9100
- Ability to document inspection results accurately using quality software or paper records
- Knowledge of statistical process control and basic root cause analysis methods
Quality Inspector Jobs in North Carolina: Frequently Asked Questions
How do you become a quality inspector in North Carolina?
North Carolina does not require a state-issued license to work as a quality inspector, so the path runs through education and industry credentials. Most employers start with a high school diploma plus hands-on manufacturing experience, while an associate degree in industrial technology or quality management strengthens your profile. Earning a Certified Quality Inspector credential through the American Society for Quality is the most widely recognized step up and is actively sought by North Carolina aerospace, defense, and pharmaceutical manufacturers.
Which companies hire quality inspectors in North Carolina?
Employers hiring quality inspectors in North Carolina right now include Zachry, ABB, and Pratt & Whitney, based on current listings on Migrate Mate as of November 2026. North Carolina's concentration of aerospace, automotive, and life sciences manufacturers means quality inspection roles appear across a wide range of facility sizes, from large Tier 1 suppliers to contract manufacturers supporting defense and medical device production.
Which North Carolina cities have the most quality inspector jobs?
Durham, Semora, and Raleigh account for the most quality inspector openings in North Carolina. Charlotte drives volume through its large automotive and industrial manufacturing base, Greensboro draws demand from aerospace component suppliers and logistics operations, and the Research Triangle benefits from pharmaceutical and life sciences manufacturers that require rigorous incoming and in-process inspection staffing.
Are there remote quality inspector jobs in North Carolina?
Yes, but they're rare. Quality inspection is a fundamentally hands-on role tied to physical product, equipment, or production lines, so most positions require on-site presence. About 0% of quality inspector openings tied to North Carolina are remote or hybrid as of November 2026, and those tend to be audit coordination, supplier quality management, or documentation review roles rather than floor inspection positions.
How can I get hired as a quality inspector in North Carolina with little or no experience?
The most realistic entry path is through a production associate or manufacturing technician role at a North Carolina plant, where you build familiarity with quality checkpoints and measurement tools before moving into a dedicated inspection position. Large employers in the Charlotte and Triad regions regularly hire for these adjacent roles. Completing an industrial technology program at a North Carolina community college and pursuing a Certified Quality Inspector credential through the American Society for Quality signals commitment and gives you a measurable edge over other applicants without direct inspection experience.
Where can I find and apply to quality inspector jobs in North Carolina?
You can find and apply to quality inspector jobs in North Carolina on Migrate Mate, which lists current openings from employers actively hiring in the state. Find the roles that fit your experience and location, then apply directly to each one.
See All 94 Quality Inspector Jobs in North Carolina
Find roles in North Carolina that match your experience and apply in just a few clicks.
Find Quality Inspector Jobs