QA Manager Jobs in North Carolina
QA Manager jobs in North Carolina are in steady demand, concentrated in the state's pharmaceutical and life sciences manufacturing corridor, technology firms in the Research Triangle, and aerospace and defense suppliers near Fayetteville and Charlotte. The heaviest hiring is in Raleigh, Durham, and Charlotte, where employers such as Novo Nordisk, Lenovo, and Fresenius Medical Care maintain significant operations and regularly seek qa managers at every level from associate to senior director. The most in-demand specialties are pharmaceutical GMP compliance, software quality assurance, and medical device quality systems. Find a role that fits below and apply directly.
Find QA Manager JobsOverview
Showing 5 of 122+ QA Manager jobs
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 Manager Jobs in North Carolina
Find roles in North Carolina that match your experience and apply in just a few clicks.
Find QA Manager JobsQA Manager Jobs by City in North Carolina
Where North Carolina roles are concentrated, by current openings.
QA Manager 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
- Chemicals & Materials
- Manufacturing
- Food & Beverage
- Medical Devices
- Staffing & Recruiting
What North Carolina Employers Look For
The qualifications that appear most often in QA manager jobs across North Carolina.
- Bachelor's degree in engineering, life sciences, or a related technical field
- Five or more years of quality assurance experience with at least two in a leadership role
- Working knowledge of GMP, ISO 9001, or FDA 21 CFR Part 820 regulations
- Demonstrated experience leading audits, CAPA processes, and corrective action programs
- Proficiency with quality management systems such as Veeva Vault, MasterControl, or similar platforms
- Certifications such as ASQ Certified Quality Manager or Certified Quality Engineer preferred by many North Carolina employers
QA Manager Jobs in North Carolina: Frequently Asked Questions
How do you become a qa manager in North Carolina?
Most qa manager roles in North Carolina require a bachelor's degree in engineering, life sciences, or a related discipline, combined with progressive quality assurance experience. The state has no universal licensing board for qa managers, but roles in pharmaceutical manufacturing often require demonstrated GMP competency, and medical device positions expect familiarity with FDA quality system regulations. Certifications from the American Society for Quality, such as the Certified Quality Manager credential, strengthen candidacy considerably in the Research Triangle and Charlotte markets.
Which companies hire qa managers in North Carolina?
Employers hiring qa managers 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 dense concentration of pharmaceutical manufacturers along the I-40 corridor and major technology firms in the Research Triangle Park area means sustained, recurring demand from large, established organizations rather than sporadic startup hiring.
Which North Carolina cities have the most qa manager jobs?
Charlotte, Raleigh, and Durham lead for qa manager openings in North Carolina. Raleigh and Durham are driven by the Research Triangle's pharmaceutical, biotech, and technology sectors, while Charlotte's presence as a major financial and advanced manufacturing hub generates consistent demand from both regulated-industry manufacturers and large corporate quality functions across its surrounding counties.
Are there remote qa manager jobs in North Carolina?
Yes, though availability depends heavily on the sector. About 32% of qa manager openings tied to North Carolina are remote or hybrid as of August 2026, reflecting a mix of on-site manufacturing roles and desk-based quality positions. Remote arrangements are most common for software quality assurance and quality systems roles, while pharmaceutical, medical device, and aerospace positions generally require on-site presence for audits, line walks, and lab oversight.
How can I get hired as a qa manager in North Carolina with little or no experience?
The most realistic path is moving into quality from an adjacent role such as QA analyst, quality technician, lab associate, or production supervisor in one of North Carolina's pharmaceutical or manufacturing facilities. Companies like Pfizer's Sanford plant and the many contract manufacturers along the Research Triangle's biotech corridor hire quality coordinators and specialists as entry points. Earning an ASQ Certified Quality Improvement Associate credential and building hands-on CAPA and audit experience in those roles positions candidates for a management step within a few years.
Where can I find and apply to qa manager jobs in North Carolina?
You can find and apply to qa manager jobs in North Carolina on Migrate Mate, which lists current openings from employers across the state. Search the available roles, find positions that fit your background and location, and apply directly to the ones that match.
See All 122+ QA Manager Jobs in North Carolina
Find roles in North Carolina that match your experience and apply in just a few clicks.
Find QA Manager Jobs