QA Specialist Jobs in North Carolina
QA Specialist jobs in North Carolina are in steady demand, with consistent hiring across pharmaceutical manufacturing, contract research organizations, medical device companies, and technology firms at levels from entry-level technician through senior quality engineer. The strongest concentrations of openings are in the Research Triangle area, Charlotte, and Wilmington, where employers like Pfizer, Labcorp, and Lenovo have established operations. The most sought-after specialties in North Carolina include FDA-regulated manufacturing quality, software QA and test automation, and clinical quality assurance. Find a role that fits below and apply directly.
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Cosette Pharmaceuticals, Inc. is a US-based, fully integrated pharmaceutical company with capabilities in product development, manufacturing, and commercial operations. Cosette has a fast-growing portfolio of branded pharmaceuticals consisting of products in the cardiology, women's health, and migraine markets. Cosette has a long history in quality manufacturing of complex dosage forms including topical creams, ointments, oral liquids/solutions and suppositories, which has led to consistent supply to customers and commercialization success. Cosette has corporate and manufacturing facilities in New Jersey and North Carolina and is supported by more than 300 dedicated employees across all functional areas.
Innovating every day.™
Basic Purpose:
Provide QA support to Manufacturing & Packaging. Ensure finished product complies with all regulatory requirements through review of batch documentation in accordance with appropriate SOPs and GMPs. Ability to perform listed tasks independently.
Essential Functions and Responsibilities:
- Perform 1st and 2nd check on completed batch documentation per applicable SOPs and GMPs.
- Perform record correction verification and product release.
- Identify and quarantine non-compliant material.
- Interact positively within Production Support Team, and internal / external customers.
- Interact and co-ordinate with other departments as necessary to complete QA tasks successfully; assists with resolution of issues providing feedback on investigation of non-compliant situations.
- Support Packaging and Manufacturing issues. Utilize knowledge of SOPs and GMPs to resolve quality issues. Communicate details of issues to team members and supervision.
- Perform QA Line Support activities including verification and release procedures, end of run reviews, QA checks.
- Ability to approve ProCal reports for metrology.
- Use departmental tracking tools (i.e., databases, etc.). Perform necessary Inventory Control functions (release, quarantine, etc.). Administer the Deviation system.
- Adhere to and enforce internal quality systems and procedures. Utilize knowledge of SOPs and GMPs to resolve quality issues.
- Other duties as assigned.
Knowledge, Skills, Qualifications and Physical Requirements:
The following describes the general knowledge, skills, qualifications, and physical requirements normally associated with performing the essential functions of this job. In compliance with law Cosette Laboratories will consider varying or modifying these standards to provide individuals with disabilities an equal employment opportunity.
Education/Training/Work Experience:
- Associates Degree in analytical field of study or two (2) plus years of applicable experience.
- Relevant work experience may be considered as a substitute for education requirement.
Specialized Knowledge and Skills:
- Relevant experience in pharmaceutical environment.
- Leadership qualities, interpersonal and team building skills.
- Good problem solving, organization, documentation and communication skills.
- Good working knowledge of PCs and Microsoft applications.
Equipment and Applications:
- Microsoft Applications, Inventory Control, and Veeva
Work Environment and Physical Demands (List required PPE’s):
- Ability to occasionally lift 50 pounds.
- Ability to sit at a workstation for extended periods of time.
Cosette Pharmaceuticals, Inc. is a US-based, fully integrated pharmaceutical company with capabilities in product development, manufacturing, and commercial operations. Cosette has a fast-growing portfolio of branded pharmaceuticals consisting of products in the cardiology, women's health, and migraine markets. Cosette has a long history in quality manufacturing of complex dosage forms including topical creams, ointments, oral liquids/solutions and suppositories, which has led to consistent supply to customers and commercialization success. Cosette has corporate and manufacturing facilities in New Jersey and North Carolina and is supported by more than 300 dedicated employees across all functional areas.
Innovating every day.™
Basic Purpose:
Provide QA support to Manufacturing & Packaging. Ensure finished product complies with all regulatory requirements through review of batch documentation in accordance with appropriate SOPs and GMPs. Ability to perform listed tasks independently.
Essential Functions and Responsibilities:
- Perform 1st and 2nd check on completed batch documentation per applicable SOPs and GMPs.
- Perform record correction verification and product release.
- Identify and quarantine non-compliant material.
- Interact positively within Production Support Team, and internal / external customers.
- Interact and co-ordinate with other departments as necessary to complete QA tasks successfully; assists with resolution of issues providing feedback on investigation of non-compliant situations.
- Support Packaging and Manufacturing issues. Utilize knowledge of SOPs and GMPs to resolve quality issues. Communicate details of issues to team members and supervision.
- Perform QA Line Support activities including verification and release procedures, end of run reviews, QA checks.
- Ability to approve ProCal reports for metrology.
- Use departmental tracking tools (i.e., databases, etc.). Perform necessary Inventory Control functions (release, quarantine, etc.). Administer the Deviation system.
- Adhere to and enforce internal quality systems and procedures. Utilize knowledge of SOPs and GMPs to resolve quality issues.
- Other duties as assigned.
Knowledge, Skills, Qualifications and Physical Requirements:
The following describes the general knowledge, skills, qualifications, and physical requirements normally associated with performing the essential functions of this job. In compliance with law Cosette Laboratories will consider varying or modifying these standards to provide individuals with disabilities an equal employment opportunity.
Education/Training/Work Experience:
- Associates Degree in analytical field of study or two (2) plus years of applicable experience.
- Relevant work experience may be considered as a substitute for education requirement.
Specialized Knowledge and Skills:
- Relevant experience in pharmaceutical environment.
- Leadership qualities, interpersonal and team building skills.
- Good problem solving, organization, documentation and communication skills.
- Good working knowledge of PCs and Microsoft applications.
Equipment and Applications:
- Microsoft Applications, Inventory Control, and Veeva
Work Environment and Physical Demands (List required PPE’s):
- Ability to occasionally lift 50 pounds.
- Ability to sit at a workstation for extended periods of time.
See All 122+ QA Specialist Jobs in North Carolina
Find roles in North Carolina that match your experience and apply in just a few clicks.
Find QA Specialist JobsQA Specialist Jobs by City in North Carolina
Where North Carolina roles are concentrated, by current openings.
QA Specialist Job Market in North Carolina
A snapshot from current North Carolina openings, updated as new roles post.
Who's Hiring
- Food Lion38
- Voltage5
- NV54
- Vaarg2
- Valicy2
Top Industries Hiring
- Biotechnology & Pharmaceuticals
- Chemicals & Materials
- Consulting & Professional Services
- Manufacturing
- Medical Devices
What North Carolina Employers Look For
The qualifications that appear most often in QA specialist jobs across North Carolina.
- Bachelor's degree in life sciences, engineering, computer science, or a related field
- Experience with quality management systems such as ISO 9001 or FDA 21 CFR regulations
- Familiarity with test documentation, defect tracking, and quality audit procedures
- Proficiency in QA tools such as JIRA, Selenium, or laboratory information management systems
- Strong written communication skills for producing SOPs, deviation reports, and test plans
- ASQ Certified Quality Auditor or Certified Quality Engineer credential preferred by many employers
QA Specialist Jobs in North Carolina: Frequently Asked Questions
How do you become a qa specialist in North Carolina?
Most qa specialist roles in North Carolina require a bachelor's degree in a relevant field such as engineering, life sciences, or computer science. There is no state-issued license specific to qa specialists in North Carolina, but employers in FDA-regulated industries strongly favor candidates who hold American Society for Quality credentials such as the Certified Quality Auditor or Certified Quality Engineer. Building experience through internships with Research Triangle pharmaceutical or medical device companies gives candidates a significant practical edge.
Which companies hire qa specialists in North Carolina?
Employers hiring qa specialists in North Carolina right now include Food Lion, Voltage, and NV5, based on current listings on Migrate Mate as of August 2026. North Carolina's concentration of pharmaceutical manufacturers, contract research organizations, and technology firms in the Research Triangle and Charlotte metro areas makes it one of the more active states for consistent qa specialist recruitment.
Which North Carolina cities have the most qa specialist jobs?
Charlotte, Raleigh, and Durham have the most qa specialist openings in North Carolina. The Research Triangle anchors the largest share of demand because of its dense cluster of pharmaceutical manufacturers, biotechnology firms, and contract research organizations, while Charlotte's finance and manufacturing base drives steady hiring and Wilmington's growing life sciences corridor has expanded the number of available positions there.
Are there remote qa specialist jobs in North Carolina?
Yes, and they're more common than in many technical fields. About 31% of qa specialist openings tied to North Carolina are remote or hybrid as of August 2026, reflecting the strong software QA and clinical data review segments of the market. Roles focused on test automation, regulatory document review, and clinical quality assurance tend to offer the most remote flexibility, while positions requiring hands-on inspection of physical products or laboratory environments remain predominantly on-site.
How can I get hired as a qa specialist in North Carolina with little or no experience?
The most realistic entry path is targeting associate quality technician or QA analyst roles at North Carolina pharmaceutical and medical device manufacturers, many of which run structured new-hire development programs for candidates with a relevant degree but limited work history. Companies like Labcorp and the large contract manufacturers in the Research Triangle and Wilmington corridors regularly hire recent graduates into entry-level quality control or document control positions. Earning an entry-level ASQ certification or completing a quality systems coursework program strengthens an application considerably for these openings.
Where can I find and apply to qa specialist jobs in North Carolina?
You can find and apply to qa specialist jobs in North Carolina on Migrate Mate, which lists current openings from employers hiring in the state right now. Search the listings for roles that match your experience and specialty, then apply directly to the ones that fit.
See All 122+ QA Specialist Jobs in North Carolina
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