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Associate Director Quality Assurance Jobs (NOW HIRING)

AGC Biologics

Director, Quality Assurance

Bothell, WA

$164K - $226K/yr

Job Summary We are looking for a Director, Quality Assurance to lead QA operations supporting GMP manufacturing of biologics. This role provides both strategic direction and daytoday leadership ...

Hearst

Director, Quality Assurance

Tampa, FL · Hybrid

The Director, Quality Assurance is a hybrid-based opportunity in Tampa that will lead and scale a modern quality engineering and automation organization. This role is responsible for defining and ...

Bachem

Director, Quality Assurance

Vista, CA · On-site

$167K - $230K/yr

A brief overview The Director of Quality Assurance, in conjunction with the VP of Quality, maintains systems to assure compliance regulatory and client requirements for all relevant GMP operations ...

AstraZeneca

Director Quality Assurance

Rockville, MD · On-site

$174K - $262K/yr

Join us as a Director Quality Assurance , where you will lead and direct the Site Quality Assurance Operations at our Cell Therapy 9950 MCD Rockville manufacturing site. This role offers an ...

Bachem

Director, Quality Assurance

Vista, CA

$167K - $230K/yr

A brief overview The Director of Quality Assurance, in conjunction with the VP of Quality, maintains systems to assure compliance regulatory and client requirements for all relevant GMP operations ...

AstraZeneca

Director Quality Assurance

Rockville, MD · On-site

$174K - $262K/yr

Join us as a Director Quality Assurance , where you will lead and direct the Site Quality Assurance Operations at our Cell Therapy 9950 MCD Rockville manufacturing site. This role offers an ...

AstraZeneca

Director Quality Assurance

Rockville, MD

$174K - $262K/yr

Join us as a Director Quality Assurance , where you will lead and direct the Site Quality Assurance Operations at our Cell Therapy 9950 MCD Rockville manufacturing site. This role offers an ...

AstraZeneca

Director Quality Assurance

Rockville, MD

$174K - $262K/yr

Join us as a Director Quality Assurance, where you will lead and direct the Site Quality Assurance Operations at our Cell Therapy 9950 MCD Rockville manufacturing site. This role offers an ...

Away

Director, Quality Assurance

New York, NY · On-site

$150K - $165K/yr

Join The Crew We are hiring a Director of Quality Assurance to lead our Quality team. This role reports to the Head of Operations and takes Away further by owning the strategic roadmap to optimize ...

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Associate Director Quality Assurance information

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

As of Jun 15, 2026, the average hourly pay for associate director quality assurance in the United States is $29.29, according to ZipRecruiter salary data. Most workers in this role earn between $18.75 and $34.38 per hour, depending on experience, location, and employer.

What are Associate Director Quality Assurance roles and responsibilities?

An Associate Director of Quality Assurance is responsible for overseeing the quality assurance processes within an organization to ensure products and services meet established standards and regulatory requirements. This role typically involves developing and implementing quality management systems, leading audits, managing QA teams, and collaborating with other departments to improve process efficiency and compliance. The Associate Director ensures that all quality objectives are met and often serves as a key point of contact during inspections and regulatory reviews.

What are the key skills and qualifications needed to thrive as an Associate Director Quality Assurance, and why are they important?

To thrive as an Associate Director Quality Assurance, strong expertise in quality management systems, regulatory compliance, and a relevant degree (such as in life sciences or engineering) are essential. Familiarity with industry standards like ISO 9001, FDA regulations, and proficiency with quality management software or audit tools are typically required. Leadership, critical thinking, and excellent communication help drive continuous improvement and foster cross-functional collaboration. These skills ensure robust quality processes, regulatory adherence, and the consistent delivery of safe, effective products.

What are the most common challenges faced by an Associate Director of Quality Assurance in balancing regulatory compliance and operational efficiency?

One of the main challenges for an Associate Director of Quality Assurance is maintaining strict adherence to regulatory standards while also supporting operational efficiency. This role often requires navigating evolving regulations, implementing robust quality management systems, and ensuring all team members are trained on compliance protocols. Additionally, balancing the need for thorough documentation and audits with the demands of production timelines can be complex. Success in this position involves strong cross-departmental collaboration, proactive risk management, and clear communication to align quality goals with business objectives.

What is the difference between Associate Director Quality Assurance vs Quality Assurance Manager?

AspectAssociate Director Quality AssuranceQuality Assurance Manager
CredentialsBachelor's or Master’s in Life Sciences, Quality Assurance certifications (e.g., ASQ)Bachelor's in Life Sciences, Quality certifications often preferred
Work EnvironmentStrategic oversight, cross-department collaboration, senior-level responsibilitiesOperational focus, team management, process implementation
Industry UsagePharmaceutical, biotech, medical devicesPharmaceutical, biotech, medical devices
Search/Comparison IntentUnderstanding senior QA roles, strategic responsibilitiesOperational QA roles, team management

The Associate Director Quality Assurance typically holds a higher strategic and leadership role compared to a Quality Assurance Manager. While both roles require similar credentials and industry experience, the Associate Director focuses on overseeing quality strategies across departments, whereas the QA Manager manages daily operations and team activities. The choice depends on your career level and focus within quality assurance.

More about Associate Director Quality Assurance jobs
What cities are hiring for Associate Director Quality Assurance jobs? Cities with the most Associate Director Quality Assurance job openings:
What states have the most Associate Director Quality Assurance jobs? States with the most job openings for Associate Director Quality Assurance jobs include:
What job categories do people searching Associate Director Quality Assurance jobs look for? The top searched job categories for Associate Director Quality Assurance jobs are:
Associate Director Quality Assurance jobs near you
Infographic showing various Associate Director Quality Assurance job openings in the United States as of June 2026, with employment types broken down into 1% Locum Tenens, 1% As Needed, 74% Full Time, 4% Part Time, 1% Temporary, and 19% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $60,925 per year, or $29.3 per hour.
AD/Director, Quality Assurance

AD/Director, Quality Assurance

AdeptSource

Redwood City, CA

Other

Posted 10 days ago

Job description

Title: AD/Director, Quality Assurance, Pharma
Location: Redwood City, CA
Type of role: FTE, Full time Salary: 181K - 214K plus bonus and equity
Our direct client is seeking an Associate Director / Director Quality Assurance to join their growing company.
Job Description
  • Develop and implement GXP including GMP quality systems in accordance with ICH, FDA, EMA and global competent authority regulations and industry guidance
  • Review all GXP documents/reports especially as they relate to method development, validation activities and PPQ generation results
  • Provide compliance oversight for internal and contracted external GXP activities
  • Coordinate and implement audit plans and audit reports for all CROs, CDMOs, and GMP vendors and internal departments.
  • Coordinate and perform virtual or on-site audits as needed
  • Provide quality oversight for GMP CDMOs (including quality agreements) and manage GMP product batch record review and disposition.
  • Lead and ensure inspection readiness activities for all internal and external entities
  • Host GMP inspections. Follow up to any responses and CAPAs
  • Develop, implement, and manage the quality management systems including vendor management, change control, product label review, risk management, GXP computer systems, deviation and CAPA systems
  • Develop and implement overall GXP strategy, performance metrics, analytics, and reports
  • Ensure and record periodic SOP trainings for all employees including onboarding FTEs and contractors in the GXP system as applicable
Qualifications
  • Bachelor's degree in biological sciences or related field with minimum of 10 years' experience in a pharmaceutical setting.
  • Proven, extensive knowledge of worldwide GXP regulatory requirements, industry practices, and ability to apply concepts. Experience with GMP regulations and current industry standards.
  • Experience in designing and implementing quality systems and risk management tools
  • Experience interacting with and managing CMOs for DS and DP especially biological products
  • Experience leading/hosting US and international health authority inspections/interactions
  • Excellent interpersonal, verbal, and written communication skills are critical in our collaborative work environment
  • Must demonstrate high organizational, prioritization and management proficiencies
  • Ability to deliver in a fast-paced, small company environment and tenacity to seamlessly adjust workload based upon changing priorities

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