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Assurance Director Jobs (NOW HIRING)

Certified Group

Quality Assurance Director

Burbank, CA · On-site

Job Summary The Corporate Quality Director is responsible for the leadership, oversight, and continuous improvement of the Quality Assurance function and Quality Management System (QMS) across ...

Certified Group

Quality Assurance Director

Burbank, CA · On-site

Job Summary The Corporate Quality Director is responsible for the leadership, oversight, and continuous improvement of the Quality Assurance function and Quality Management System (QMS) across ...

Compass Group

QUALITY ASSURANCE DIRECTOR

Boston, MA

$108K/yr

Job Summary The Food Safety & Quality Assurance Director ensures that multiple food service locations-operate with the highest standards of food safety, sanitation, and product quality. This role ...

Compass Group

QUALITY ASSURANCE DIRECTOR

Boston, MA · On-site

$108K/yr

Job Summary The Food Safety & Quality Assurance Director ensures that multiple food service locations-operate with the highest standards of food safety, sanitation, and product quality. This role ...

ARGO

Director Of Quality Assurance

Richardson, TX

JOB SUMMARY The QA Director is a leadership role responsible for driving both strategic and tactical quality execution across ARGO's Software Development Life Cycle (SDLC) and customer initiatives.

Exelixis

Compliance QA Director

Alameda, CA · On-site

The Compliance QA Director leads the company's GxP inspection readiness ensuring ongoing preparedness for global health authority inspections. This role manages regulatory inspections and responses ...

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Assurance Director information

See salary details

$56.5K

$140.1K

$227.5K

How much do assurance director jobs pay per year?

As of Jul 4, 2026, the average yearly pay for assurance director in the United States is $140,083.00, according to ZipRecruiter salary data. Most workers in this role earn between $103,000.00 and $169,000.00 per year, depending on experience, location, and employer.

What is the difference between Assurance Director vs Audit Manager?

AspectAssurance DirectorAudit Manager
CredentialsCPA or equivalent, extensive experience in assuranceCPA or equivalent, several years of audit experience
Work EnvironmentStrategic oversight, senior leadership, client relationship managementLeading audit teams, executing audit procedures, reporting
Employer & IndustryAccounting firms, corporations, consulting firmsPublic accounting firms, internal audit departments

The Assurance Director focuses on strategic assurance initiatives and client relationships, while the Audit Manager handles day-to-day audit operations and team management. Both roles require similar credentials but differ in scope and seniority.

What does an assurance director do?

An assurance director oversees the internal and external audit processes to ensure financial statements are accurate and comply with regulations. They lead audit teams, review financial controls, and communicate findings to stakeholders, often requiring certifications like CPA and strong knowledge of accounting standards. Their role involves strategic planning and risk management within an organization’s financial reporting environment.

What is the salary of QA vs QC?

For an Assurance Director or similar quality assurance roles, salaries for QA (Quality Assurance) and QC (Quality Control) professionals vary based on experience, industry, and location. Generally, QA roles focus on process improvement and prevention, often commanding higher salaries, while QC roles focus on product inspection and testing. Entry-level positions may start lower, but experienced QA managers can earn significantly higher salaries, often supplemented with certifications like Six Sigma or ISO standards.

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

To thrive as an Assurance Director, you need deep expertise in accounting, auditing standards, and risk assessment, typically supported by a CPA or similar professional qualification. Mastery of audit software, data analytics tools, and familiarity with regulatory compliance systems is crucial. Outstanding leadership, critical thinking, and communication skills set top performers apart by enabling effective team management and client relationships. These abilities ensure high-quality audit outcomes, regulatory compliance, and the sustained trust of stakeholders.

How does an Assurance Director typically collaborate with cross-functional teams within an organization?

Assurance Directors frequently work with departments such as finance, operations, IT, and legal to ensure compliance with regulatory standards and internal controls. They lead audit teams, coordinate with management to address risk areas, and facilitate the implementation of best practices. Effective communication and strong leadership are essential, as the Assurance Director often translates complex audit findings into actionable insights for various stakeholders. This collaborative approach helps foster a culture of transparency and continuous improvement across the organization.

How much does a QA director make in the US?

A QA (Quality Assurance) Director in the US typically earns between $100,000 and $160,000 annually, with the median around $130,000. Salaries vary based on experience, industry, and location, and the role often requires strong leadership, quality management skills, and familiarity with testing tools and methodologies.

What does a QA manager earn?

A QA manager's salary typically ranges from $70,000 to $130,000 annually, depending on experience, industry, and location. They often oversee quality assurance teams, develop testing procedures, and use tools like test management software to ensure product quality.
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Assurance Director jobs near you
Quality Assurance Director

Quality Assurance Director

Evolution Research Group

Miami, FL • On-site

Full-time

Medical, Dental, Retirement, PTO

Posted 11 days ago

Job description

About Company:

Evolution Research Group (ERG) is dedicated to delivering high-quality Phase I–IV clinical trial execution to help sponsors bring lifesaving and life-enhancing therapies to market quickly and safely. Founded in 2014, ERG has grown into a leading neuroscience clinical development company, with affiliate sites across the U.S. and deep expertise in clinical pharmacology, psychiatry, neurology, acute pain, and metabolic disorders. ERG has completed over 5,000 trials and continues to expand into high-need therapeutic areas in the U.S. and globally.

Why join us? We offer a supportive culture, meaningful work, and the opportunity to contribute to cutting-edge research alongside industry leaders. Plus, we offer competitive benefits include medical and dental coverage, a matching 401(k), and paid time off to recharge.

Location: Miami (Onsite)

Job Description:

This role is based at our largest site, Clinical Pharmacology of Miami (CPMI). The Director’s primary role is for ensuring that day-to-day clinical trial operations at the CPMI site are conducted in compliance with study protocols, FDA regulations, and ICH/GCP guidelines. This role provides oversight and reporting to Operational Leadership to maintain the integrity and quality of all site activities. This is a leadership role, and the ideal candidate will have experience mentoring and leading others.

Oversight and communication with the Operational Team may include (but is not limited to):

  • Conducting internal audits
  • Monitoring training completion and associated metrics
  • Providing support and consultation for Quality events and CAPAs
  • Overseeing and assisting with internal and external audits
  • Managing and supervising Quality Control plans and QC staff
  • Maintaining all Quality-related activities within the clinic

Additionally, this role is part of the ERG Corporate Quality Assurance Team, a mobile unit that provides coverage across all ERG portfolio sites. Responsibilities include supporting the overall Quality Management System for these sites to ensure quality assurance, quality control, compliance, and auditing activities related to study conduct.

As needed, or in the absence of the Vice President of Quality Assurance, this role may assume leadership of the ERG Corporate QA Team, oversee the planning, execution, and analysis of Quality Assurance initiatives, as well as managing external audits for the organization. This position reports directly to the Vice President of QA.

In fulfilling these responsibilities, the CPMI-based Quality Assurance and Compliance Director operates in alignment with FDA regulations, Good Clinical Practice (GCP) guidelines, and the company’s standard operating procedures and policies.

Responsibilities:

Quality Management of the Clinic

  • Lead and conduct audits of study documents, Case Report Forms, Clinical Study Reports, and other supporting documentation to ensure compliance
  • Collaborate with Site Director and study PIs to resolve and document issues promptly and effectively
  • Conduct GCP compliance audits of vendors in accordance with Standard Operating Procedures
  • Report significant Quality issues to Vice President, Quality Assurance
  • Oversee the implementation of corrective actions with support of the Site Director and VP of Quality
  • Responsible for facilitating Sponsor Audits and assisting with other Sponsor site visits as applicable (and to report results of audits to Vice President, QA)
  • Assist with supporting Regulatory (FDA, EMA, etc) Inspections and preparation activities
  • Oversee training is conducted in accordance with SOPs and reports metrics to Operational Leadership for required management and next steps.
  • Responsible to oversee all Document Control activities for the site, and for other sites as requested from the VP of QA.
  • Ensure the appropriateness and effectiveness of site CAPA investigations and oversee timely and accurate reporting of results to applicable stakeholders, including Sponsors, CROs, and IRBs.
  • Responsible to fully manage all aspects of the electronic Quality Management System as it applies to CPMI (and to ERG as a whole under the direction of the VP of Quality).
  • Play a key role in site leadership and client engagement, ensuring clear communication, professionalism, and alignment with Operational Leadership and the Quality Assurance Department.
  • Supervise direct reports supporting Quality Assurance and Quality Control efforts on clinical trials.

ERG Corporate QA Team (Quality Mobile Unit)

  • Member of a professional team focused on clinical quality assurance/quality control and compliance-related activities in support of clinical programs and activities.
  • Assist in maintaining ERGs Quality Management System (QMS), inclusive of the eQMS, to ensure compliance to Good Clinical Practice (GCP) and that the QMS is aligned with the internal policies and standard operating procedures for ERG.
  • Assist in audit activities in the areas of Vendor Audit Management, facilitation of internal & external clinical quality audits, and agency inspections
  • Participate in the oversight of Corrective and Preventive Actions (CAPA) implementation and assist in conducting Quality reviews.
  • Perform any other tasks/duties assigned by VP QA
  • Potential travel to other ERG portfolio sites to assist with QA initiatives, internal audits, regulatory inspection support, etc as applicable and assigned.

Skills and Qualifications:

  • Education and experience
  • Thorough understanding of Good Clinical Practices (GCP), Code of Federal Regulations (CFR), and HIPAA as they apply to clinical research.
  • Bachelor’s degree or higher in life sciences, medicine, or a related field (or equivalent experience).
  • Bilingual Spanish highly preferred
  • Minimum of 10 years in the pharmaceutical, clinical, or medical device industry, including conducting internal and external audits.
  • At least 5 years of experience participating in FDA or other regulatory agency inspections (preferred).
  • Extensive experience managing CAPA programs with a focus on GCP compliance, ensuring timely completion and deliverables.
  • Background in project management, site leadership, or oversight of high-volume clinical trials strongly desired.
  • Experience with 21 CFR Part 11 and aspects of Computer System Validation (preferred but not required).
  • Requirements
  • Strong understanding of FDA regulatory requirements, Good Clinical Practice (GCP), and International Conference on Harmonization (ICH) guidelines.
  • Knowledge of medical terminology.
  • Excellent organizational and prioritization skills with the ability to adapt in a dynamic, changing environment.
  • Strong analytical and problem-solving abilities.
  • Ability to provide accurate guidance and support on regulatory requirements.
  • Excellent documentation practices and attention to detail.
  • Ability to travel as requested by the Vice President of QA.
  • Exceptional communication skills (interpersonal, written, and verbal).
  • Proficiency in computer applications, including Microsoft Word and Excel, and familiarity with clinical research systems (e.g., Clinical Trial Management Systems).