ZipRecruiter

Log In

1

Quality Assurance Qa Associate Jobs in Delaware (NOW HIRING)

Hologic

Quality Assurance Technician 3

Newark, DE · On-site

$54K - $80K/yr

Job Summary: The QA Technician 3 performs functions associated with quality assurance ... S./GED) or Associate Degree Experience * Preferred Minimum Non-Technical Degree: 2-4 Years

Sarian, Inc.

UFT QA Testing

Newark, DE · On-site

UFT QA Testing Location: Newark DE, Charlotte, Plano TX, Addison TX Onsite position Fulltime Position *****NO C2C***** JD: Skill: QA Automation Testing Must Have Technical/Functional Skills: * * 4+ ...

Hologic

Clinical QA Specialist

Newark, DE · On-site

$85K - $133K/yr

At Hologic, we are seeking a Clinical QA Specialist to play a critical role in the investigation and reporting of potential and actual adverse events, as well as other regulatory reporting activities.

Hologic

Clinical QA Specialist

Newark, DE · On-site

$85K - $133K/yr

At Hologic, we are seeking a Clinical QA Specialist to play a critical role in the investigation and reporting of potential and actual adverse events, as well as other regulatory reporting activities.

Hologic Inc.

Clinical QA Specialist

Newark, DE · On-site

$85K - $133K/yr

At Hologic, we are seeking a Clinical QA Specialist to play a critical role in the investigation and reporting of potential and actual adverse events, as well as other regulatory reporting activities.

previous pagenext page

Showing results 21-40

All JobsQuality Assurance Qa Associate JobsQuality Assurance Qa Associate Jobs in Delaware

Quality Assurance Qa Associate information

See Delaware salary details

$12

$29

$62

How much do quality assurance qa associate jobs pay per hour?

As of Aug 22, 2026, the average hourly pay for quality assurance qa associate in Delaware is $29.32, according to ZipRecruiter salary data. Most workers in this role earn between $18.75 and $34.42 per hour, depending on experience, location, and employer.

What does a quality assurance QA associate do?

A Quality Assurance (QA) Associate is responsible for ensuring that products or services meet established quality standards and regulatory requirements. They develop and implement testing procedures, conduct inspections, and identify areas for improvement in production or service processes. QA Associates work closely with other departments to resolve quality-related issues and help maintain compliance with company policies and industry regulations. Their work is essential for delivering consistent, safe, and effective products to customers.

How does a quality assurance QA associate typically interact with other departments to ensure product quality?

Quality Assurance QA Associates frequently collaborate with teams such as Production, Research & Development, and Regulatory Affairs to uphold product quality standards. They review documentation, provide feedback on process improvements, and may participate in cross-functional meetings to address quality concerns or deviations. This teamwork is essential for identifying potential issues early, ensuring compliance with regulations, and supporting a culture of continuous improvement throughout the organization.

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

To thrive as a Quality Assurance QA Associate, you need a strong understanding of quality control processes, documentation standards, and often a degree in a scientific or technical field. Familiarity with quality management systems (such as ISO standards), proficiency in data analysis tools, and experience with software like LIMS or ERP systems are typically required. Attention to detail, critical thinking, and effective communication are essential soft skills for this position. These skills ensure products meet regulatory requirements and company standards, ultimately protecting consumer safety and business reputation.

What is the difference between Quality Assurance Qa Associate vs Quality Control Inspector?

AspectQuality Assurance Qa AssociateQuality Control Inspector
Primary FocusPreventing defects through process improvementsDetecting defects in finished products
Work EnvironmentCollaborates with teams, audits, documentationInspects products on production lines or in labs
CertificationsOften requires QA certifications, ISO standards knowledgeMay require specific industry certifications, safety training
Industry UsageCommon in manufacturing, software, healthcarePrimarily in manufacturing, food, electronics

The main difference is that a Quality Assurance Qa Associate focuses on preventing defects through process improvements and audits, while a Quality Control Inspector primarily detects defects in finished products. QA associates work proactively to ensure quality standards are met, whereas QC inspectors verify product quality after production. Both roles are essential in maintaining product standards but serve different points in the quality management process.

Is a Quality Assurance Qa Associate an entry level job?

A Quality Assurance QA Associate is often an entry-level position that requires basic knowledge of testing processes, attention to detail, and familiarity with tools like test management software. Many employers provide on-the-job training, and the role typically does not require extensive prior experience or advanced certifications.

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

The most popular types of Quality Assurance Qa jobs in Delaware are:

What are popular job titles related to Quality Assurance Qa Associate jobs in Delaware?

For Quality Assurance Qa Associate jobs in Delaware, the most frequently searched job titles are:

What job categories do people searching Quality Assurance Qa Associate jobs in Delaware look for?

The top searched job categories for Quality Assurance Qa Associate jobs in Delaware are:

Quality Assurance Qa Associate jobs near you
Infographic showing various Quality Assurance Qa Associate job openings in Delaware as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 15% Part Time, 4% Contract, and 1% Nights. Highlights an 87% Physical, 2% Hybrid, and 11% Remote job distribution, with an average salary of $60,977 per year, or $29.3 per hour.

Quality Assurance Specialist - Pharmaceuticals

WuXi AppTec

Middletown, DE • On-site

Other

Re-posted 23 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.

Apply