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

Quality Assurance

Cary, NC · On-site

$18.50/hr

Ability to manage multiple priorities in a fast-paced environment. * Basic math skills, including ... Quality Assurance * Attention to Detail * Communication Skills * Organization and Planning

Assurance Manager

Raleigh, NC

$108K - $130K/yr

About the Role The Assurance Manager oversees engagements from start to finish, managing the client relationship and internal engagement teams to ensure the quality and timeliness of client ...

Assurance Manager

Raleigh, NC

$108K - $130K/yr

About the Role The Assurance Manager oversees engagements from start to finish, managing the client relationship and internal engagement teams to ensure the quality and timeliness of client ...

Quality Assurance

Morrisville, NC · On-site

$18.50 - $18.88/hr

For Quality Assurance in Durham, Cary, and Morrisville - RTP. These opportunities come with ... What We're Looking For · Ability to manage multiple priorities in a fast-paced environment. · ...

For Quality Assurance in Durham, Cary, and Morrisville - RTP. These opportunities come with ... What We're Looking For · Ability to manage multiple priorities in a fast-paced environment. · ...

Senior BA & QA Specialist

Raleigh, NC · Hybrid

$80K - $110K/yr

247Hire in Raleigh, North Carolina seeks a Senior Business Analyst / Tester for a hybrid role that integrates business analysis with software quality assurance testing. The successful candidate will ...

Showing results 41-60

Senior Qa Manager information

See Raleigh, NC salary details

$27.7K

$94.4K

$177.4K

How much do senior qa manager jobs pay per year?

As of Aug 7, 2026, the average yearly pay for senior qa manager in Raleigh, NC is $94,384.00, according to ZipRecruiter salary data. Most workers in this role earn between $47,600.00 and $132,700.00 per year, depending on experience, location, and employer.

How does a senior QA manager typically collaborate with cross-functional teams to ensure product quality?

A Senior QA Manager works closely with development, product management, and operations teams to align testing activities with business goals and release schedules. They facilitate regular meetings to discuss quality objectives, review test strategies, and coordinate bug tracking and resolution efforts. By fostering open communication and integrating QA processes into the overall development lifecycle, Senior QA Managers help ensure that quality is a shared responsibility and that potential issues are addressed early. This collaborative approach not only improves product outcomes but also enhances team efficiency and morale.

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

To thrive as a Senior QA Manager, you need extensive experience in software quality assurance, deep knowledge of testing methodologies, and often a degree in computer science or a related field. Familiarity with automation tools (such as Selenium or JMeter), test management systems, and certifications like ISTQB are highly valued. Leadership, strategic thinking, and strong communication skills help manage teams and foster cross-functional collaboration. These capabilities ensure software quality, process efficiency, and seamless project delivery within complex development environments.

What is a senior QA manager?

Senior QA Managers are experienced professionals responsible for overseeing quality assurance processes within an organization. They lead QA teams, develop testing strategies, ensure products meet quality standards, and collaborate with other departments to improve software or product reliability. Their role often involves mentoring junior QA staff, managing resources, and driving continuous improvement in testing methodologies. Senior QA Managers also play a key part in defining quality metrics and ensuring compliance with industry regulations.

Is a senior QA manager a stressful job?

A senior QA manager role involves overseeing quality assurance processes, managing teams, and ensuring product standards, which can be demanding and sometimes stressful due to deadlines and high-quality expectations. However, stress levels vary depending on the organization, workload, and individual skills in project management and communication.
What job categories do people searching Senior Qa Manager jobs in Raleigh, NC look for? The top searched job categories for Senior Qa Manager jobs in Raleigh, NC are:
Infographic showing various Senior Qa Manager job openings in Raleigh, NC as of August 2026, with employment types broken down into 88% Full Time, 11% Part Time, and 1% Contract. Highlights an 84% Physical, 3% Hybrid, and 13% Remote job distribution, with an average salary of $94,384 per year, or $45.4 per hour.

Senior Specialist, Quality Assurance, Compliance and Supplier Quality

Oxford Biomedica

Durham, NC

$79K - $109K/yr

Other

Posted 8 days ago


Job description

Join Us in Changing Lives

 

At OXB, our people are at the heart of everything we do. We're on a mission to enable life-changing therapies to reach patients around the world-and we're looking for passionate individuals who embody our core values every day: Responsible, Responsive, Resilient, and Respectful.

Following the expansion of our US footprint with the acquisition of a new commercial-scale viral vector facility in Durham, North Carolina we have some new opportunities to join us.

We're currently recruiting for a Senior QA Specialist, Compliance and Supplier Quality to join our team. In this role, you will be responsible for providing quality oversight of suppliers and vendors supporting the manufacture, packaging, testing, and distribution of clinical and commercial gene and cell therapy products at OXB, playing a key part in advancing our mission and making a real difference.

Your responsibilities in this role would be:

  • Provide ongoing quality oversight of suppliers supporting GMP manufacturing, including raw materials, consumables, external laboratories, and transportation providers.
  • Support supplier qualification, re-qualification, and lifecycle management activities using a risk-based approach.
  • Support and/or conduct supplier audits (remote and on-site), including audit reporting, CAPA assessment, and follow-up.
  • Maintain oversight of critical and single/sole-source suppliers, including identification of supply and quality risks and development of mitigation strategies.
  • Manage supplier change notifications, ensuring appropriate internal documentation, quality risk assessment, and impact analysis in accordance with internal procedures.
  • Confirm quality and technical agreements remain current and are not adversely impacted by proposed supplier changes.
  • Provide Supplier Quality impact assessments for internally driven GMP changes and complete assigned change actions.
  • Ensure supplier-reported deviations, OOS, and other quality events are logged, assessed, investigated, and closed in accordance with internal procedures.
  • Collaborate with cross-functional SMEs to ensure timely investigation, root cause determination, and effective remediation.
  • Critically review supplier investigations and CAPAs
  • Support supplier and material quality risk assessments, including evaluation of data integrity, traceability, and supply continuity risks.

 

We are Looking For:

  • Bachelor's degree or higher in Life Sciences, Chemistry, Engineering, or related field
  • Minimum of 8 years of pharmaceutical industry experience, working in Supplier Quality role, and/or Quality/Compliance
  • Experience in biotechnology industry preferred
  • Strong knowledge of cGMP in the Pharma/Biotech industry to include FDA, EU, JP regulatory requirements as well as ICH/ISO guidelines
  • Knowledge of aseptic and sterile product manufacturing processes and testing.
  • Experience in Vendor Quality Oversight
  • Thorough knowledge of and competence in core quality processes such as change control, deviations/OOS, CAPA, and complaints

 

This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the United States.

 

About Us:

OXB is a quality and innovation-led viral vector CDMO with a mission to enable its clients to deliver life changing therapies to patients around the world. One of the original pioneers in cell and gene therapy, we have more than 30 years of experience in viral vectors; the driving force behind the majority of gene therapies.

OXB collaborates with some of the world's most innovative pharmaceutical and biotechnology companies, providing viral vector development and manufacturing expertise in lentivirus, adeno-associated virus (AAV) and adenoviral vectors. OXB's world-class capabilities span from early-stage development to commercialisation. These capabilities are supported by robust quality-assurance systems, analytical methods, and depth of regulatory expertise.

 

Why Join Us?

  •  Competitive total reward packages
  •  Wellbeing programs that support your mental and physical health
  •  Career development opportunities to help you grow and thrive
  •  Supportive, inclusive, and collaborative culture
  •  State-of-the-art labs and manufacturing facilities
  • A company that lives its values: Responsible, Responsive, Resilient,         Respect

We want you to feel inspired every day. At OXB, we're future-focused and growing fast. We succeed together-through passion, commitment, and teamwork.

Ready to Make a Difference?