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Director Qa Software Testing Jobs in Raleigh, NC

Cellectis

Director, Quality Control

Raleigh, NC · On-site

Partner cross-functionally with Manufacturing, QA, MSAT, AS&T, and Regulatory Affairs to support ... testing. * Strong understanding of data integrity principles and regulatory expectations (ALCOA+

Deloitte

QA Engineer/ QA Analyst

Raleigh, NC · On-site

Perform thorough regression testing when bugs are resolved. * Collaborate with the Test Lead and ... Communicate regularly with Engagement Managers (Directors), project team members, and ...

360 IT Professionals

QA selenium tester

Raleigh, NC · On-site

Company Description 360 IT Professionals is a Software Development Company based in Fremont ... Selenium QA with Strong Java coding. Page Object Model, JUnit, API is required Qualifications Need ...

Arete Technologies, Inc.

QA Tester

Cary, NC

We are pre-eminent service providers in the field of staff augmentation, IT Consultancy, Software ... Familiarity testing on OS X, iOS, Windows and Android Qualifications: * Strong written and verbal ...

Data Bridge Consultants

Senior QA Engineer

Cary, NC

$40/hr

The Senior QA Engineer will primarily lead quality assurance efforts within the software ... Identifying test conditions of satisfaction for user stories and testing tasks * Executing a QA ...

Focused HR Solutions

1.20. QA Tester

Raleigh, NC · On-site

$45 - $48/hr

Our direct client has an opening for a QA Tester position # 729722. This position is for 12+ months ... Requirements and Software Design Documents. * Experience in the execution of functional ...

Focused HR Solutions

8-11 QA Tester

Raleigh, NC · On-site

$35 - $47/hr

... QA and testing of web applications Required 2 Years. * Experience assessing the testability of requirements and developing test cases based on Business Requirements and Software Design Documents.

Focused HR Solutions

8-11 QA Tester

Raleigh, NC · On-site

$35 - $47/hr

... QA and testing of web applications Required 2 Years. * Experience assessing the testability of requirements and developing test cases based on Business Requirements and Software Design Documents.

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 ...

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Director Qa Software Testing information

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

As of Jun 8, 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.
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Director Qa Software Testing jobs near you

Director, Quality Control

Cellectis

Raleigh, NC • On-site

Full-time

Posted 4 days ago

Job description

Job Description
POSITION SUMMARY
The Director, Quality Control provides strategic and operational leadership for all Quality Control (QC) activities supporting drug substance (DS) and dug product (DP) manufacturing at the site. This role is accountable for ensuing the generation of accurate, reliable, and compliant analytical data to support product release, stability, and lifecycle management in accordance with global GMP requirements.
The Director QC oversees all QC functions, including analytical, microbiological, and environmental monitoring programs, and ensures alignment with the overall control strategy. This role ensures inspection readiness data integrity, and continuous improvement of QC systems and processes. As a member of the site Quality Leadership Team, the Director partners cross-functionally with Manufacturing m QA, MSAT, AS&T, and Regulatory to support clinical and commercial manufacturing while advancing quality culture and operational excellence.
POSITION RESPONSIBILITIES
  • Provide strategic leadership and oversight of all QC activities supporting DS and DP manufacturing, including release testing, stability programs, and in-process testing.
  • Partner with AS&T to ensure the robustness and lifecycle management of the analytical control strategy including method qualification, validation, transfer, and performance monitoring.
  • Oversee analytical, microbiological, and environmental monitoring programs, ensuring compliance with GMP requirements and site contamination control strategy
  • Ensure data integrity, accuracy, and reliability of all QC data in accordance with regulatory expectations.
  • Establish and maintain inspection readiness, including hosting regulatory inspections and responding to health authority inquiries.
  • Drive timely and thorough investigations of OOS, OOT, and atypical results, ensuring appropriate root cause identification and effective CAPA implementation.
  • Ensure appropriate specifications, test methods, and acceptance criteria are established and maintained throughout the product lifecycle.
  • Oversee QC laboratory operations including resource planning, capacity management, and organizational capability development
  • Partner cross-functionally with Manufacturing, QA, MSAT, AS&T, and Regulatory Affairs to support batch release, process improvements, and regulatory submissions.
  • Lead continuous improvement initiatives to enhance laboratory efficiency, compliance, and right-first-time performance.
  • Develop and monitor QC performance metrics, identifying trends and driving actions to improve performance and compliance.
  • Build and develop a high performing QC organization, fostering a strong quality culture and technical excellence.
  • Participates in business sub-teams as a Subject Matter Expert (SME) to provide input on timeliness and to address analytical/microbiological related issues
  • Other responsibilities and duties as the company may from time-to-time assign

EDUCATION AND EXPERIENCE
  • Bachelor's degree in chemistry, Biology or related scientific discipline required, advanced degree preferred.
  • Minimum 12 years of experience in pharmaceutical or biotechnology QC, with. 8 years in leadership roles.
  • Strong leadership skills with experience building and leading high-performing technical teams.
  • Experience managing environmental monitoring and contamination control strategies in GMP manufacturing environments.
  • Experience supporting DS & DP manufacturing in GMP environments.
  • Proven track record of regulatory inspection success and audit management.
  • Proven experience with laboratory method lifecycle management.
  • Experience implementing or optimizing laboratory systems and processes preferred.

TECHNICAL SKILLS / CORE COMPETENCIES
  • Deep expertise in GMP regulations applicable to QC laboratories supporting ATMPs.
  • Strong knowledge of analytical techniques (e.g. q/rt/ddPCR, flow cytometry, ELISA, cell-based assays, microbiological methods) and their application tin DS/DP testing.
  • Strong understanding of data integrity principles and regulatory expectations (ALCOA+).
  • Ability to operate effectively in a matrixed, cross-functional environment.
  • Strong problem-solving skills with a risk-based and science-driven approach.
  • Excellent communication skills with the ability to influence at site and executive levels.
  • Strong project management skills.

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