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Associate Director Quality Assurance Jobs in Boca Raton, FL

TekSky

Quality Assurance Manager

West Palm Beach, FL · On-site

Director of Quality Assurance Employment Type: Full-Time Job Summary: The Quality Manager is responsible for leading and developing the Quality team while ensuring full compliance with 21 CFR Part ...

5TH HQ LLC

Quality Assurance Inspector

Plantation, FL · On-site

... Control Associate in the Pre-Press Department. In this role, you will play a crucial part in ... Follow established procedures for quality assurance and communicate effectively with team members ...

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Associate Director Quality Assurance information

See Boca Raton, FL salary details

$12

$27

$58

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

As of Sep 4, 2026, the average hourly pay for associate director quality assurance in Boca Raton, FL is $27.80, according to ZipRecruiter salary data. Most workers in this role earn between $17.79 and $32.64 per hour, depending on experience, location, and employer.

What are the roles and responsibilities of an associate director quality assurance?

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 skills and qualifications are needed to thrive as an associate director quality assurance?

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 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.

What are popular job titles related to Associate Director Quality Assurance jobs in Boca Raton, FL?

For Associate Director Quality Assurance jobs in Boca Raton, FL, the most frequently searched job titles are:

What job categories do people searching Associate Director Quality Assurance jobs in Boca Raton, FL look for?

The top searched job categories for Associate Director Quality Assurance jobs in Boca Raton, FL are:

What cities near Boca Raton, FL are hiring for Associate Director Quality Assurance jobs?

Cities near Boca Raton, FL with the most Associate Director Quality Assurance job openings:

Associate Director Quality Assurance jobs near you
Infographic showing various Associate Director Quality Assurance job openings in Boca Raton, FL as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 16% Part Time, 3% Contract, and 1% Nights. Highlights an 84% Physical, 1% Hybrid, and 15% Remote job distribution, with an average salary of $57,815 per year, or $27.8 per hour.

Quality Assurance Manager

TekSky

West Palm Beach, FL • On-site

Full-time

Re-posted 24 days ago

Job description

Job Title: Quality Assurance Manager
Department: Quality
Reports To: Director of Quality Assurance
Employment Type: Full-Time
Job Summary:
The Quality Manager is responsible for leading and developing the Quality team while ensuring
full compliance with 21 CFR Part 111 and all applicable regulatory, customer, and internal
quality standards. This role oversees quality systems, documentation control, investigations,
supplier qualification, audit management, and customer quality support to ensure product safety,
compliance, and continuous improvement.
Key Responsibilities:
• Manage and develop the Quality team through daily oversight, performance management,
coaching, and ongoing GMP and SOP training.
• Ensure compliance with 21 CFR Part 111 through implementation, monitoring, and
execution of Standard Operating Procedures (SOPs) across the facility.
• Lead regulatory and third-party audits, including audit preparation, hosting, coordination, and
timely response to audit findings.
• Manage employee training compliance, including onboarding, GMP training, SOP training,
qualification programs, and maintenance of training records.
• Own and maintain Master Manufacturing Records (MMRs), Batch Production Records
(BPRs), and controlled documentation systems to ensure accuracy and regulatory
compliance.
• Own and manage deviation, nonconformance, Out-of-Specification (OOS), and CAPA
investigations through root cause analysis and timely closure.
• Manage supplier qualification programs, including supplier approval, raw material risk
assessments, performance monitoring, and ongoing supplier evaluations.
• Ensure product labeling, specifications, and formulations meet regulatory requirements and
customer specifications prior to release.
• Execute and oversee change control activities impacting product quality, safety, compliance,
or documentation.
• Manage customer quality agreements, technical questionnaires, and routine quality inquiries
to ensure alignment with regulatory and contractual obligations.
• Investigate and draft responses to customer complaints, conduct trend analysis, and
implement corrective or preventive actions as needed.
• Ensure audit readiness at all times and maintain programs aligned with applicable Dietary
Supplement cGMP standards.
• Support manufacturing and packaging operations to ensure adherence to quality and product
safety standards.
• Lead internal audit programs to verify compliance with regulatory requirements, cGMPs, and
internal procedures.
• Collect, analyze, and trend quality data to identify opportunities for continuous improvement
and risk mitigation.
• Perform other duties as assigned by management.
Qualifications:
• Bachelor's degree in Food Science, Quality Management, Biology, Chemistry, or
a related scientific field.
• 5+ years of experience in quality assurance within dietary supplement, food, or
pharmaceutical manufacturing.
• Strong working knowledge of 21 CFR Part 111, cGMP requirements, FDA
regulations, and quality systems management.
• Experience managing audits, CAPA systems, supplier qualification programs,
and regulatory inspections.
• Proven leadership experience with the ability to train, mentor, and develop
quality personnel.
• Strong analytical, organizational, and problem-solving skills.
• Excellent written and verbal communication skills.
• Proficiency in document control systems and quality management software.
Additional Skills:
• Strong leadership and decision-making abilities.
• High problem-solving skills in fast-paced manufacturing environments.
• Ability to manage multiple priorities and meet deadlines.
• Analytical mindset with the ability to interpret regulations and apply them
practically.
• Computing skills (Word, Excel, PowerPoint) to generate reports and maintain
records.
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About Teksky

Sourced by ZipRecruiter

Industry

It services and recruiting and staffing services

Company size

11 - 50 Employees

Headquarters location

Sterling, VA, US

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