ZipRecruiter

Log In

1

Director Qa Software Testing Jobs in Raleigh, NC

Cellectis

Director, Clinical Quality Assurance

Raleigh, NC · On-site

$190K - $2M/yr

The Director, Clinical Quality Assurance is primarily responsible for establishing and leading the Clinical QA function and providing independent oversight of Good Clinical Practices (GCP) activities ...

DivIHN

QA Contractor, GMP Quality Assurance

NC · On-site

Collaborate successfully with the other departments to ensure that direct and supportive tasks are ... Experience in analytical method validation and QC testing, especially in the fields of mammalian ...

Golden Technology

QA Manual Tester

Raleigh, NC · On-site

Your Next Career Move Starts Here Title: QA Manual Tester Location: Raleigh, NC Type : Contract We ... Support User Acceptance Testing (UAT) as needed What's In It For You * Opportunities to work on ...

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

$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 ...

Software Technology Inc

Automation QA

Raleigh, NC · On-site

QA Automation Engineer Your role as a QA Automation Engineer is to write scripts and create ... Your goal is to automate as much of the testing effort as possible with a minimum set of code.

next page

Showing results 1-20

All JobsDirector Qa Software Testing JobsDirector Qa Software Testing Jobs in Raleigh, NC

Director Qa Software Testing information

See Raleigh, NC salary details

$54.9K

$136.2K

$221.1K

How much do director qa software testing jobs pay per year?

As of Jun 26, 2026, the average yearly pay for director qa software testing in Raleigh, NC is $136,172.00, according to ZipRecruiter salary data. Most workers in this role earn between $100,100.00 and $164,300.00 per year, depending on experience, location, and employer.

What are some common challenges a Director of QA Software Testing faces when aligning testing strategies with business objectives?

One common challenge for Directors of QA Software Testing is ensuring that testing strategies not only maintain high product quality but also align with evolving business goals and timelines. Balancing comprehensive test coverage with the need for rapid releases often requires prioritization and negotiation with product and engineering teams. Additionally, managing distributed teams, integrating new testing technologies, and advocating for quality in a fast-paced environment can be complex. Strong communication and leadership skills are essential for navigating these challenges while supporting both team and organizational success.

What does a Director of QA Software Testing do?

A Director of QA (Quality Assurance) Software Testing oversees the entire quality assurance process for software development within an organization. They are responsible for establishing testing strategies, leading QA teams, ensuring software products meet quality standards, and collaborating with other departments to improve development practices. This role often involves designing efficient testing processes, managing resources and budgets, and driving continuous improvement initiatives. The Director of QA Software Testing also ensures compliance with industry regulations and customer requirements, making sure that the final software products are reliable, secure, and user-friendly.

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

To thrive as a Director of QA Software Testing, you need deep expertise in software testing methodologies, quality assurance processes, and a solid background in computer science or a related field. Familiarity with automated testing tools, test management systems, and relevant certifications such as ISTQB are typically required. Strong leadership, strategic thinking, and excellent communication skills help you manage teams and collaborate across departments. These competencies ensure the delivery of reliable software products, effective risk management, and alignment of QA initiatives with organizational goals.
What are the most commonly searched types of Qa Software Testing jobs in Raleigh, NC? The most popular types of Qa Software Testing jobs in Raleigh, NC are:
What are popular job titles related to Director Qa Software Testing jobs in Raleigh, NC? For Director Qa Software Testing jobs in Raleigh, NC, the most frequently searched job titles are:
What job categories do people searching Director Qa Software Testing jobs in Raleigh, NC look for? The top searched job categories for Director Qa Software Testing jobs in Raleigh, NC are:
What cities near Raleigh, NC are hiring for Director Qa Software Testing jobs? Cities near Raleigh, NC with the most Director Qa Software Testing job openings:
Director Qa Software Testing jobs near you
Sr. Quality Assurance Specialist

Sr. Quality Assurance Specialist

Asklepios BioPharmaceutical, Inc.

Durham, NC • On-site

$79K - $109K/yr

Full-time

Posted 11 days ago

Job description

AskBio Inc., a wholly owned and independently operated subsidiary of Bayer AG, is a fully integrated gene therapy company dedicated to developing life-saving medicines and changing lives. The company maintains a portfolio of clinical programs across a range of neuromuscular, central nervous system, cardiovascular, and metabolic disease indications with a clinical-stage pipeline that includes investigational therapeutics for congestive heart failure, limb-girdle muscular dystrophy, multiple system atrophy, Parkinson's disease, and Pompe disease. AskBio's gene therapy platform includes Pro10™, an industry-leading proprietary cell line manufacturing process, and an extensive array of capsids and promoters. With global headquarters in Research Triangle Park, North Carolina, and European headquarters in Edinburgh, Scotland, the company has generated hundreds of proprietary capsids and promoters, several of which have entered pre-clinical and clinical testing.
Our vision: Pioneering science to create transformative molecular medicines.
Our mission: Lead innovative science and drive clinical outcomes to transform people's lives.
Our principles:
  • Advance innovative science by pushing boundaries.
  • Bring transformative therapeutics to patients in need.
  • Provide an environment for employees to reach their fullest potential.

Our values:
  • Be a Pioneer. We are not afraid of the impossible and to innovate to make gene therapies accessible to those in need.
  • Cultivate Collaboration. Strive to be the best teammate, actively listen, openly communicate, and embrace diverse points of view.
  • Embrace Responsibility. We are humbled by the enormity of our mission. We hold a relentless commitment to advance science and clinical outcomes for our patients, families, and caregivers.
  • Raise the Bar. Continuously drive improvements and efficiencies. Seek and provide constructive feedback. Have a bias for learning and action.
  • Act with Uncompromising Integrity. Be honest, transparent, and committed to doing what's right in every situation. Make clear commitments and follow through.

The Senior Specialist, Quality Assurance provides Quality Assurance (QA) oversight of AskBio's Vendor Qualification Program for GCLP, GLP, GCP (and GMP vendors, as needed). This key individual performs vendor assessments and occasional audits (virtual and on-site) alongside subject matter experts, ensuring vendor qualification activities support compliance with applicable GLCP, GLP, GCP, and GMP guidelines and relevant national/international/local regulations. This position will work closely with the GCP/GLP/GCLP QA and SMEs.
This position will be office-based in RTP, NC and will report to the Senior Director, QA - Product Quality.
Job Responsibilities
  • Maintain and manage a risk-based model for qualification and quality oversight of GCLP, GCP, GLP vendors (and GMP vendors, as needed). in compliance with AskBio SOPs
  • Assure the conduct of regular vendor assessments or audits of GCLP, GCP, GLP (and GMP vendors, as needed).to evaluate regulatory compliance, performance, and improvement opportunities (via questionnaire and/or audit), involving GCP/GLP/GCLP QA and SMEs, as appropriate
  • Serve as primary interface with GCP/GLP/GCLP QA and related functional area staff on topics relevant to vendor qualification
  • Identify, track status, and schedule audits and assessments of GCLP, GCP, GLP (and GMP vendors, as needed). vendors
  • Advance the Vendor Qualification program by identifying opportunities and implementing risk-appropriate enhancements to program infrastructure
  • Support functional area staff to resolve vendor observations and quality issues, including risk/impact assessment and CAPA development, execution, and effectiveness checks
  • Maintain and evolve mechanisms that ensure awareness and application of Vendor Qualification QMS requirements
  • Contribute to the development, implementation, and maintenance of SOPs, Policies, and Quality Agreements
  • Support coordination and management of regulatory agency inspections and parent company audits, as appropriate
  • Perform other duties as assigned by Quality Assurance Management
  • Travel may be required to perform audits (approximately 20%)

Minimum Requirements
  • Bachelor's degree in science, health care, business, or other relevant field and 5+ years of relevant industry experience
  • Knowledge of industry best practices and regulatory requirements, including, Good Clinical Laboratory Practices (GCLP), Good Laboratory Practices (GLP), Good Clinical Practices (GCP)
  • Experience in vendor qualification or vendor management
  • Strong collaborative skills; ability to work cross-functionally in a matrixed environment
  • Ability to proactively and diplomatically identify and resolve quality issues/discrepancies
  • Ability to prioritize, organize, work independently, and manage multiple projects/tasks simultaneously
  • Analytical mindset with strong attention to detail
  • Excellent interpersonal, verbal, and written communication skills
  • Proficiency in MS Word, Excel, PowerPoint, and other applications

Preferred Education, Experience and Skills
  • Laboratory, clinical research, and/or Quality Assurance (or related) experience
  • Audit experience, including ASQ certification for auditing (CQA) or similar
  • Knowledge of Good Manufacturing Practices (GMP)

AskBio Inc. (AskBio) is an Equal Opportunity Employer and does not discriminate against any employee or applicant for employment because of race, color, religion, gender, sexual orientation, gender identity, national origin, age, disability, veteran status or any other protected status prohibited under Federal, State or local laws. All employment decisions are based on valid job-related requirements. If you are a qualified individual with a disability or a disabled veteran and are unable or limited in your ability to use or access our website, you may request a reasonable accommodation to express interest in a specific opening by calling us at (919) 561-6210 or sending us an email at careers@askbio.com.
Agencies: Please do not contact any employee at AskBio about this requisition. Any resume submitted by a recruitment agency to any employee at AskBio, through any medium, will be deemed the sole property of AskBio unless the agency was engaged by AskBio Talent Acquisition team to recruit for that position. All agencies must have a prior executed service agreement with AskBio prior to any search engagement. If a candidate who was submitted outside of the AskBio agency process is hired by AskBio, no fee or payment of any kind will be paid to the agency.

Apply