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Functional Qa Jobs in Raleigh, NC (NOW HIRING)

Senior Quality Assurance Engineer

Raleigh, NC ยท On-site

$86K - $126K/yr

The Senior QAE works closely with Global Quality Assurance Leadership, Engineering Leadership, Program Managers, Product Owners, and cross-functional teams to ensure compliance with corporate quality ...

Senior Quality Assurance Engineer

Raleigh, NC ยท On-site

$86K - $126K/yr

The Senior QAE works closely with Global Quality Assurance Leadership, Engineering Leadership, Program Managers, Product Owners, and cross-functional teams to ensure compliance with corporate quality ...

Quality Assurance leader in Information Technology responsible for leading teams of QA Engineers ... Prior experience supporting large, complex, enterprise and cross functional programs and/or ...

This role oversees QA's day-to-day activities and resolution or mitigation of issues. Company ... Collaborative attitude; willingness to work with global peers and cross-functional teams toward ...

The QA Specialist, Drug Product (DP) helps drive the Quality oversight for the direction of all DP ... Collaborative attitude; willingness to work with global peers and cross-functional teams toward ...

This role oversees QA's day-to-day activities and resolution or mitigation of issues. Company ... Collaborative attitude; willingness to work with global peers and cross-functional teams toward ...

8-11 QA Tester

Raleigh, NC ยท On-site

$35 - $47/hr

Our client has an opening for a QA Tester 735026 This position is up to 12 months, with the option ... Experience in the execution of functional, integration and regression tests. Required 5 Years.

QA Engineer, Validation

Holly Springs, NC ยท On-site

$62K - $80K/yr

Position Overview The QA Engineer, Validation is responsible for helping to drive the Quality ... Collaborative attitude with the willingness to work with global peers and cross-functional teams ...

QA Engineer, Validation

Holly Springs, NC ยท On-site

$62K - $80K/yr

Position Overview The QA Engineer, Validation is responsible for helping to drive the Quality ... Collaborative attitude with the willingness to work with global peers and cross-functional teams ...

Participate in cross-functional teams to resolve quality and process-related issues. * Minimal to no travel required * Strong analytical and problem-solving skills. * Ability to manage multiple ...

Showing results 41-60

Functional Qa information

See Raleigh, NC salary details

$10

$39

$69

How much do functional qa jobs pay per hour?

As of Sep 10, 2026, the average hourly pay for functional qa in Raleigh, NC is $39.01, according to ZipRecruiter salary data. Most workers in this role earn between $27.36 and $47.88 per hour, depending on experience, location, and employer.

What is the difference between Functional Qa vs Manual Qa?

AspectFunctional QaManual Qa
CertificationsISTQB, CSTE, CSQAISTQB, CSTE, CSQA
Work EnvironmentTest teams, software development projectsTest teams, software development projects
Industry UsageCommon in software and application testingCommon in software and application testing
FocusTesting specific functionalities and featuresExecuting test cases manually without automation

Functional Qa focuses on testing specific features and functionalities of software, often using test cases derived from requirements. Manual Qa involves executing test cases manually without automation tools. While both roles are essential in software testing, Functional Qa emphasizes verifying that features work as intended, whereas Manual Qa is more about the process of executing tests without automation tools.

What cities near Raleigh, NC are hiring for Functional Qa jobs?

Cities near Raleigh, NC with the most Functional Qa job openings:

Infographic showing various Functional Qa job openings in Raleigh, NC as of August 2026, with employment types broken down into 1% As Needed, 89% Full Time, 6% Part Time, and 4% Contract. Highlights an 83% Physical, 5% Hybrid, and 12% Remote job distribution, with an average salary of $81,142 per year, or $39 per hour.

Quality Engineer II-III, Quality Assurance

Durham, NC โ€ข On-site

MedPharm
Pharmaceutical and Medicine Manufacturingย โ€ขย 11 - 50 employees

Full-time

Posted 17 days ago


Job description

Position Summary
Quality Engineer II-III, Quality Assurance is responsible for designing, implementing, and maintaining the Quality Management System across the manufacturing lifecycle. This role supports process validation; root-cause investigations for deviations; oversees Corrective and Preventive Actions; and ensures compliance with current Good Manufacturing Practices. This position is responsible for monitoring and control the quality processes supporting incoming, in-process and final disposition including batch record review and release for GMP, clinical, and commercial programs through broad knowledge of GLP/GMP manufacturing theories and principles. This position works closely with other functional areas of the Company to release raw materials, per agreed upon timelines. Additional areas of responsibility include QA oversight of operational metrics and supporting client and internal auditing activities. The Quality Engineer II-III, Quality Assurance shall adhere to the Company's quality system including but not limited to the applicable standards, policies and procedures in the areas of responsibility defined in this job description.
Essential Functions
  • Regulatory Compliance: Ensure all production practices strictly align with FDA 21 CFR Parts 210/211, ICH Q10, and global cGMP standards.
  • Validation & Qualification: Quality Assurance review and approval of validation protocols (IQ/OQ/PQ) for manufacturing equipment, facilities, utilities, and analytical laboratory software.
  • Deviation & CAPA Management: Support investigation of manufacturing deviations and out-of-specification (OOS) results using root-cause analysis tools like 5 Whys and Fishbone diagrams.
  • Documentation: Quality Assurance review and approval of manufacturing documentation, including specifications, batch records, and batch release.
  • Risk Assessment: Support Quality Risk Management (QRM) initiatives utilizing Failure Mode and Effects Analysis (FMEA) to minimize patient and product risk.
  • Change Control Oversight: Evaluate and approve change controls for processes, materials, or equipment to ensure they do not negatively impact product quality.
  • Audit Support: Conduct routine internal audits and manage readiness documentation for external regulatory agency inspections.
  • Supplier Quality: Partner with procurement to audit third-party raw material suppliers and manage external quality issues.
  • Oversee the quality management processes ensuring that client requirements, specifications, and regulatory requirements are met by the Operations Unit.
  • Collaborate with cross-functional teams, including production, engineering, supply chain, and customer service, to address quality issues and drive continuous improvement initiatives.
  • Analyze quality data and performance metrics to identify trends, root causes of defects, and opportunities for process optimization.
  • Partner with Operations supporting closure of Quality Events and quality improvement plans when needed.
  • Conduct regular audits to monitor compliance with quality standards and identify areas for improvement.
  • Routinely draft and revise standard operating procedures and QA review of master batch records.
  • Leads internal and supports external audits in accordance with Company procedures and schedules. Develop reports of audit findings and communicate these to the relevant project team and to Company management

Direct Reports: No
Indirect Reports: No
Key Relationships (examples: Depts or Individual positions that this position will be working closely with):
  • Manufacturing Operations
  • Warehouse
  • Quality Control

Travel requirements
  • N/A

Education and Experience
  • B.A. / B.S. in a Engineering discipline, or equivalent experience preferred
  • Quality Assurance experience in the pharmaceutical industry for 5 +years

Knowledge, Skills, and Abilities
  • Knowledge of Pharmaceutical Quality Management Systems requirements and execution
  • Demonstrated proficiency in written, verbal and face-to-face communication to effectively present information to internal and external customers
  • Ability to successfully manage multiple tasks and multifunctional resources concurrently while maintaining high attention to detail while responding to rapidly changing priorities and aggressive deadlines
  • Technically capable of identifying root cause of a problem, offering potential solutions, and engaging with others to resolve the problem
  • Produces consistent, high quality and quantity of outputs and meaningful results that contribute to the agency mission and strategic goal. Is efficient in producing results that are delivered on time or before.
  • Ability to work independently and as part of a team
  • Expertise in MS Office (Excel, Word, Outlook, Project) and Adobe Pro

Physical Demands and Work Environment
While performing the duties of this job, there may be certain physical demands required for the position.
  • Requires frequent standing
  • Requires constant walking
  • Requires occasional sitting
  • Requires frequent carrying, bending, twisting, reaching, & gripping
  • Requires frequent lifting, pushing, & pulling 20-60 LBS

Other Duties
You may be asked to take on any other responsibilities or tasks that are within your skills and abilities whenever reasonably asked.
Limitations and Disclaimer
The above job description is meant to describe the general nature and level of work being performed; it is not intended to be construed as an exhaustive list of all responsibilities, duties, and skills required for the position. The Company is committed to making reasonable adjustments to the workplace to ensure the role is accessible to all candidates, including those with disabilities. To perform the job successfully, the employee must possess the abilities or aptitudes to perform each duty proficiently.