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Qa Director Jobs in Delaware (NOW HIRING)

The Summit

Quality Assurance Nurse

Hockessin, DE · On-site

$85K/yr

We are seeking a dedicated Quality Assurance Nurse to help us ensure the highest quality of care ... Partners with Director of Health and Wellness (DHW) and other team members to analyze and maintain ...

The Summit

Quality Assurance Nurse

Hockessin, DE · On-site

$85K/yr

We are seeking a dedicated Quality Assurance Nurse to help us ensure the highest quality of care ... Partners with Director of Health and Wellness (DHW) and other team members to analyze and maintain ...

The Summit

Quality Assurance Nurse

Hockessin, DE · On-site

$85K/yr

We are seeking a dedicated Quality Assurance Nurse to help us ensure the highest quality of care ... Partners with Director of Health and Wellness (DHW) and other team members to analyze and maintain ...

THE SUMMIT

Quality Assurance Nurse

Hockessin, DE

$85K/yr

We are seeking a dedicated Quality Assurance Nurse to help us ensure the highest quality of care ... Partners with Director of Health and Wellness (DHW) and other team members to analyze and maintain ...

The Summit

Quality Assurance Nurse

Hockessin, DE · On-site

We are seeking a dedicated Quality Assurance Nurse to help us ensure the highest quality of care ... Partners with Director of Health and Wellness (DHW) and other team members to analyze and maintain ...

The Summit

Quality Assurance Nurse

Hockessin, DE · On-site

$85K/yr

We are seeking a dedicated Quality Assurance Nurse to help us ensure the highest quality of care ... Partners with Director of Health and Wellness (DHW) and other team members to analyze and maintain ...

KBR

Specialist, Quality Assurance

Wilmington, DE · On-site

Specialist, Quality Assurance KBR Sustainable Technology Solutions (STS) provides holistic and ... Under general supervision, and occasional direct supervision, the incumbent performs assignments ...

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All JobsQa JobsQa Director JobsQa Director Jobs in Delaware

Qa Director information

See Delaware salary details

$56.5K

$140.2K

$227.7K

How much do qa director jobs pay per year?

As of Aug 19, 2026, the average yearly pay for qa director in Delaware is $140,204.00, according to ZipRecruiter salary data. Most workers in this role earn between $103,100.00 and $169,100.00 per year, depending on experience, location, and employer.

What does a QA director do?

A QA Director, or Quality Assurance Director, is responsible for overseeing the entire quality assurance process within an organization. They develop and implement testing strategies, ensure products meet quality standards, and lead teams of QA professionals. The QA Director works closely with other departments to identify quality issues and drive continuous improvement. Their role is crucial in delivering reliable, high-quality products to customers.

What are some common challenges a QA director faces when building and leading a quality assurance team?

A QA Director often encounters challenges such as aligning quality goals with rapidly changing project requirements, balancing manual and automated testing strategies, and ensuring effective communication between QA teams and other departments like development and product management. Additionally, recruiting and retaining skilled QA professionals, fostering a culture of continuous improvement, and keeping up with evolving industry standards are frequent hurdles. Successful QA Directors address these challenges by promoting collaboration, investing in team training, and implementing scalable QA processes.

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

To thrive as a QA Director, you need deep expertise in quality assurance methodologies, leadership experience, and a background in computer science or a related field. Familiarity with test automation tools, QA management systems, and relevant certifications like ISTQB or Six Sigma are commonly expected. Strong strategic thinking, effective communication, and the ability to inspire and manage cross-functional teams are standout soft skills. These qualifications ensure the delivery of high-quality products, streamlined QA processes, and alignment between quality goals and overall business objectives.

Is QA a stressful job?

The QA Director role can be stressful due to responsibilities like managing testing processes, meeting project deadlines, and ensuring product quality. It often requires strong organizational skills, attention to detail, and the ability to handle multiple priorities under tight schedules.

What are the most commonly searched types of Qa jobs in Delaware?

The most popular types of Qa jobs in Delaware are:

What cities in Delaware are hiring for Qa Director jobs?

Cities in Delaware with the most Qa Director job openings:

Qa Director jobs near you
Infographic showing various Qa Director job openings in Delaware as of August 2026, with employment types broken down into 2% As Needed, 81% Full Time, 14% Part Time, 1% Temporary, and 2% Contract. Highlights an 91% Physical, 3% Hybrid, and 6% Remote job distribution, with an average salary of $140,204 per year, or $67.4 per hour.

Quality Assurance Specialist - Pharmaceuticals

WuXi AppTec

Middletown, DE • On-site

Other

Re-posted 20 days ago

Job description

Overview
Company Overview
WuXi STA is building new pharmaceutical manufacturing capability and is establishing the quality systems that will support it. For more information, see:
New manufacturing facility announcement
About the company
Responsibilities
The Quality Assurance Specialist is a fully qualified quality professional who provides independent, on-the-floor quality assurance support to manufacturing and operations while the site's GMP quality system is being established. This is a build role rather than a maintenance role: the Specialist helps stand up the quality processes, systems, and documentation required for Oral Solid Dosage (OSD) and Sterile drug-product manufacturing-including aseptic processing and drug-substance operations-and ensures compliance with applicable GMP regulations and health-authority expectations.
Working with limited precedent, the Specialist exercises independent judgment to resolve quality issues of diverse scope, advises operations and cross-functional partners, and helps embed a "Right First Time" culture as the site progresses toward routine GMP operations. Work is performed independently and reviewed at critical points.
Key Responsibilities
  • Provide independent on-the-floor quality assurance support to manufacturing and operations, including real-time batch record review and timely disposition of quality events during production.
  • Help establish and document the site quality management system (QMS), authoring and improving SOPs, work instructions, and job aids for sterile/aseptic and drug-product operations to meet FDA, EMA, and other applicable health-authority requirements.
  • Own quality events end to end-deviations, investigations, root-cause analysis, CAPAs, change controls, and effectiveness checks-applying structured problem-solving to events of diverse scope and limited precedent.
  • Review commissioning, qualification, and validation (CQV) documentation, including URS, FAT/SAT, turnover packages, IQ/OQ/PQ, and process validation.
  • Lead readiness inspections of manufacturing areas, equipment, computerized systems, and processes to identify and mitigate quality risks prior to operational start-up.
  • Support new product introduction (NPI) and technology-transfer activities, providing quality oversight of batch records, bills of materials, and related documentation to enable right-first-time execution.
  • Design and deliver quality and GMP training, and coach operations and quality colleagues to build capability and a sustained "Right First Time" culture during this formative period.
  • Serve as a quality subject-matter expert for internal, client, and regulatory inspections, and advise stakeholders toward sound and compliant decisions.
  • Ensure complete, accurate, and contemporaneous records in accordance with Good Documentation Practices and data-integrity (ALCOA+) principles, including appropriate use of electronic QMS and document-management systems and other validated digital quality tools.
  • Partners across manufacturing, engineering, and validation functions to integrate quality requirements into daily operations.

Qualifications
  • Bachelor's degree in scientific or engineering discipline, or an equivalent combination of education and directly relevant experience.
  • Approximately five years of pharmaceutical or biopharmaceutical quality assurance experience, or an equivalent combination of education and directly relevant experience, including hands-on time in a GMP manufacturing environment.
  • Experience supporting a greenfield site or new-facility start-up and standing up QMS processes from the ground up, or experience with New Product Introduction (NPI).
  • Experience working in a multiproduct pharmaceutical manufacturing facility, including managing differing customer requirements and the controls used to prevent cross-contamination between products.
  • Demonstrated, hands-on understanding of both manufacturing/production operations and quality assurance.
  • Direct experience with sterile drug-product manufacturing and aseptic processing in a GMP setting.
  • Demonstrated ownership of core QMS elements-deviations, investigations, root-cause analysis, CAPA, and change control-including the ability to explain the rationale and compliance basis behind each.
  • Working knowledge of applicable GMP regulations and ICH guidelines, and the ability to apply them to operational decisions.
  • Strong Good Documentation Practices and data-integrity (ALCOA+) discipline.
  • Experience operating within an electronic quality and/or document management system.
  • Excellent written and verbal communication, with the ability to influence and align stakeholders across functions and levels.
  • Ability to work independently with limited precedent, exercising sound judgment and seeking review at critical decision points.Experience with electronic QMS / document-management platforms such as Veeva Vault and SAP.
  • Experience supporting audits and inspections, including backroom management and subject-matter-expert preparation.
  • Quality or auditing certification (for example, ASQ CQA, CQE, or CMQ/OE).
  • Familiarity with risk-management tools (for example, FMEA) and statistical process control concepts.
  • Composed and credible in client-facing and inspection settings.
  • Familiarity with AI regulations to ensure the data is secure and understanding of the data-integrity and confidentiality risks associated with unvalidated AI tools.

  • Key Competencies
  • Right First Time mindset: drives quality at the source and coaches others to do the same.
  • Collaborative, organized, and systematic; brings structure to ambiguous and evolving situations.
  • Clear communicator who adapts to both technical and non-technical audiences.
  • Comfortable contributing in a dynamic, build-stage environment.
  • Work Environment and Physical Requirements
    • Work in a GMP manufacturing environment, including cleanroom and classified areas that require gowning and adherence to aseptic behaviors.
    • Periods of standing, walking, and on-floor presence during production.
    • Occasional travel for audits.

An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability
This job description does not state or imply that the above are the only duties and responsibilities assigned to this position. Employees holding this position will be required to perform any other job-related duties as requested by Management.

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