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Software Qa Manager Jobs in Raleigh, NC (NOW HIRING)

DivIHN

QA Contractor, GMP Quality Assurance

NC · On-site

Manage assigned day-to-day QA responsibilities in support of the company's Quality Management Systems (QMS). * Provide timely support of Learning Management System, Change Control, Deviation ...

AskBio

Sr. Quality Assurance Specialist

Durham, NC · On-site

$79K - $109K/yr

Speak with your direct manager to discuss your interest and alignment with your development goals ... The Senior Specialist, Quality Assurance provides Quality Assurance (QA) oversight of AskBio ...

AskBio

Sr. Quality Assurance Specialist

Durham, NC · On-site

$79K - $109K/yr

Speak with your direct manager to discuss your interest and alignment with your development goals ... The Senior Specialist, Quality Assurance provides Quality Assurance (QA) oversight of AskBio ...

Belcan

Quality Assurance Inspector

Clayton, NC

$17 - $25/hr

Quality Assurance Inspector (2nd shift) Location: Clayton, NC Pay rate: $17 - $25/hr. Zip Code ... management as well as with support and service departments. Ability to work in a team-oriented ...

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Software Qa Manager information

See Raleigh, NC salary details

$11.7K

$115.3K

$161.9K

How much do software qa manager jobs pay per year?

As of Jul 15, 2026, the average yearly pay for software qa manager in Raleigh, NC is $115,331.00, according to ZipRecruiter salary data. Most workers in this role earn between $106,900.00 and $135,600.00 per year, depending on experience, location, and employer.

What does a Software QA Manager do?

A Software QA Manager oversees the quality assurance process for software development projects. Their responsibilities include developing testing strategies, managing QA teams, setting quality standards, and ensuring that software products meet both functional and performance requirements before release. They coordinate between developers, testers, and stakeholders to identify and resolve issues, and they implement best practices to improve product quality. Additionally, they may be involved in hiring, training, and evaluating the performance of QA staff.

What are the key skills and qualifications needed to thrive as a Software QA Manager, and why are they important?

To thrive as a Software QA Manager, you need expertise in software testing methodologies, quality assurance processes, and often a degree in computer science or a related field. Familiarity with test automation tools (such as Selenium or JUnit), bug tracking systems, and knowledge of Agile or Scrum frameworks are typically required, along with relevant certifications like ISTQB. Strong leadership, communication, and problem-solving skills set exceptional QA Managers apart by fostering team collaboration and effective issue resolution. These skills and qualifications are essential to ensure software quality, timely delivery, and continuous improvement within development teams.

What are some common challenges faced by Software QA Managers when leading a diverse testing team?

Software QA Managers often face challenges such as balancing tight project deadlines with the need for thorough testing, coordinating communication between developers, testers, and product managers, and ensuring consistent testing standards across both manual and automated processes. Managing a team with varying experience levels and technical backgrounds requires strong leadership and mentorship to foster collaboration and continuous learning. Additionally, adapting to changing requirements and integrating new testing tools or methodologies can be demanding, but it also provides opportunities for professional growth and innovation within the team.
What are the most commonly searched types of Software Qa jobs in Raleigh, NC? The most popular types of Software Qa jobs in Raleigh, NC are:
What are popular job titles related to Software Qa Manager jobs in Raleigh, NC? For Software Qa Manager jobs in Raleigh, NC, the most frequently searched job titles are:
What job categories do people searching Software Qa Manager jobs in Raleigh, NC look for? The top searched job categories for Software Qa Manager jobs in Raleigh, NC are:
What cities near Raleigh, NC are hiring for Software Qa Manager jobs? Cities near Raleigh, NC with the most Software Qa Manager job openings:
Software Qa Manager jobs near you
Infographic showing various Software Qa Manager job openings in Raleigh, NC as of July 2026, with employment types broken down into 81% Full Time, 16% Part Time, 1% Temporary, and 2% Contract. Highlights an 86% Physical, 1% Hybrid, and 13% Remote job distribution, with an average salary of $115,331 per year, or $55.4 per hour.

QA Contractor, GMP Quality Assurance

DivIHN

NC • On-site

Contractor

Posted 27 days ago

Job description

For further inquiries regarding the following opportunity, please contact our Talent Specialist, Hema at (630) 847-0275
Title:QA Contractor, GMP Quality Assurance
Location: Onsite at Research Triangle Park, NC
Duration: 9 Months
Travel: Domestic travel (less than 10% of the time) expected.
Only W2 candidates are eligible for this position. Third-party or C2C candidates will not be considered
Description:
The QA Contractor, GMP Quality Assurance, reporting to the Manager, GMP Quality Assurance, or designee, will be responsible for assisting in the management of client Quality Management System (QMS) and will strongly support client's Culture of Quality. This role will assure corporate compliance with applicable GMP national, international, and state regulations. This position will be based at our headquarters facility in RTP, NC.
Job Responsibilities
  • Manage assigned day-to-day QA responsibilities in support of the company's Quality Management Systems (QMS).
  • Provide timely support of Learning Management System, Change Control, Deviation Management Systems, or other QMS based customer requests.
  • Liaison with applicable department record owners to ensure their complete and timely resolution. Review and Approve said record types as assigned.
  • Provide accurate and timely weekly and quarterly QMS metric and Key Performance Indicator updates to QA and CMC senior management.
  • Collaborate successfully with the other departments to ensure that direct and supportive tasks are completed within project timelines.
  • Providing deliverables and resolving issues; Draft SOPs/controlled documents as well as perform quality unit review and approval of Quality Management Systems requests/ records related to Learning Management, Non-Conformance Management, CAPA management, and metric/KPI reporting.
  • Continually evaluate systems and procedures for improvement for efficiency and compliance to applicable regulatory requirements and standards.
  • Participate in project meetings as a Quality Unit representative and support colleagues by acting as a technical resource for quality and compliance related issues.
  • Perform daily customer-facing activities, as assigned by area management.
  • Maintain health of customer-facing activities such as document archival activities and notebook/logbook assignment and management.
  • Identify and collaborate with colleagues to implement continuous improvement initiatives; provide Quality Unit oversight of QMS based activities.
  • Assist in the qualification and oversight of vendors, contract manufacturers, contract laboratories, and service providers.
  • Support regulatory (FDA, EMA) and internal audits/inspections per client procedures and applicable regulatory requirements.
  • Communicate project status to stakeholders and escalate issues in a timely manner.
  • Perform and support other duties as assigned by area management.

About you
  • Bachelor's degree in a scientific field and 4+ years of experience in GMP based Quality Assurance, particularly in support/oversight of a company QMS, or 10+ years of GMP based Quality Assurance experience using a company QMS.
  • 3+ experience working within a pharmaceutical/biotech Quality Management system, such as Trackwise, ZenQMS, Veeva, is a requirement
  • Strong understanding of GMP guidelines and Quality Systems with the ability to apply GMPs in conformance to U.S. standards, and where appropriate, other regulatory authority standards.
  • Ability to author, review, and interpret Standard Operating Procedures (SOPs).
  • Ability to identify and/or resolve quality issues/discrepancies with others in a proactive, diplomatic, flexible, and constructive manner.
  • Strong attention to detail, highly organized and the ability to multitask in a fast-paced, highly interactive environment.
  • Strong service-oriented mindset with excellent verbal and written communication skills, and the ability to effectively collaborate with peers including scientific/technical colleagues.
  • Experience in analytical method validation and QC testing, especially in the fields of mammalian cell culture and Gene Therapy/Biologics based potency testing, is preferred.
  • Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint).

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