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Director Of Quality Assurance Jobs in the United States

Deputy Director of Quality Assurance and Quality Control

Honolulu Authority for Rapid Transportation

$120900 - $193488

Honolulu, HI

The role shall assist in the oversight to ensure HART's compliance with all applicable quality guidelines, regulations, rules, and generally accepted industry practices; assist in the oversight and review of HART's activities, and resolve quality assurance issues; develop and maintain liaison relationships with other governmental organizations/agencies; provide development and implementation assistance of effective training programs; and perform other duties as assigned by the DQA, ED/CEO, Deputy Executive Director/Chief Operating Officer, and Project Director. This position provides a high level of responsible, complex management and policy support to HART's Director of Quality Assurance and Quality Control (DQA) and the Executive Director/Chief Executive Officer (ED/CEO), and exercises significant delegated authority and independent judgment in overseeing both the administrative and technical aspects of the City's rail transit design and construction quality.

Director of Quality Assurance, Defense

RBC Bearings Incorporated

$142906 - $195523.5

South El Monte, California

Issues formal product process specifications and confers with other top management, customers and other representatives in the planning, scheduling, coordinating and directing of the quality assurance program in conformance with customer requirements, engineering specifications, government regulations and production schedules. About RBC Bearings Incorporated:RBC Bearings Incorporated (NYSE: RBC/RBCP) is a leading international manufacturer of highly engineered precision bearings, components and essential systems for the industrial, defense and aerospace industries.

Director of Quality Assurance

Curtiss-Wright Corporation

East Farmingdale, NY

As our Director of Quality Assurance you will report directly to the General Manager, as a Senior Leader Team member, and be responsible for directing and managing the TR Quality Management System. Our mission is to serve our country and the world by delivering safety critical precision valves and actuators, enabling US Navy operational excellence and reliable emission free power.

Director of Quality Assurance, Clinical

Caribou Biosciences, Inc.

$220000 - $235000

Berkeley, CA

Provide Clinical Quality Assurance (GCP) strategic and technical leadership and Subject Matter Expertise (SME) to clinical study teams; Partner with the teams to effect appropriate and timely documentation of quality event management, including CAPA plans in support of product pipeline. The successful candidate must have the ability to execute QA tasks independently; effectively represent QA in a GCP, PV, and GLP focused team settings and manage quality related activities related to clinical vendors, investigator sites and regulatory agencies.

Director of Quality Assurance

Zenflow

South San Francisco, CA

The innovative Spring® technology was designed with the patient experience in mind and relies on a small spring-like coil that gently props open the urethra, restoring its normal function while preserving the natural anatomy. The base pay range reflects the target range for this position, but individual pay will be determined by additional factors such as job-related skills, experience and relevant education or training.

Director of QA & Regulatory Affairs

ChromoLogic

$130000 - $170000

Monrovia, CA

Covisus Inc. (www.covisus.com) is a VC-funded spin-off from ChromoLogic that has developed an award-winning and industry-leading technology for tagless tracking of assets based on its vTag® technology. Develop and implement quality assurance strategies and regulatory compliance programs (FDA 510(k), PMA, IDE, drug approval, IND, pre-submission).

Senior Director/Executive Director, Head of GCP Quality Assurance

Nkarta, Inc.

$250000 - $340000

South San Francisco, CA

While getting better work-life balance and improving communications between groups in an early stage start up environment are two areas on which we are working, here are real, anonymous comments about or regarding why people think Nkarta is a great place to work. The successful hire will ensure high quality execution of clinical trials from first in human through commercial marketing authorization by Health Authorities for our cellular therapy drug candidates, which are predominantly CAR-NK cell-based.

Director of Quality Assurance

Judge Group

$140000 - $155000

Chicago, IL

By providing your phone number, you consent to: (1) receive automated text messages and calls from the Judge Group, Inc. and its affiliates (collectively "Judge") to such phone number regarding job opportunities, your job application, and for other related purposes. Monitor and measure product quality, conducting root cause analysis on quality issues, implementing corrective actions as needed.

Director of Quality Assurance/Regulatory Affairs

Hamilton Medical, Inc.

Reno, Nevada

Proven track record of authoring, reviewing, and approving high-quality 510(k) submissions, including substantial equivalence arguments, intended use, labeling, and responses to FDA deficiencies. Lead and oversee all formal FDA engagements, including Pre-Submissions (Q-Subs), submission meetings, interactive reviews, deficiency responses, and appeals.

Director of Regulatory Affairs & Quality Assurance (Medical Device)

Coyote Technical & Executive Sourcing

Fairfield, CT

Minimum Experience: 15 years of Quality Assurance, Quality Engineering, and Regulatory experience in a FDA regulated environment, preferably Medical Devices, Gastrointestinal. Hands-on Director who is responsible for the Regulatory Affairs and Quality Assurance strategy, policies, and procedures to ensure we follow all domestic and international guidelines and regulations.

DIRECTOR OF FOOD SAFETY AND QUALITY ASSURANCE

Pilgrim's Pride Corporation

$120000 - $175000

Greeley, CO

Provide strategic leadership, guidance, and risk management for corporate food safety and quality programs and systems including, but not limited to HACCP, Preventative Controls, SQF or other BRC-related programs, USDA Process Verified Program and customer or 3rd party audit-driven requirements and policies. For individuals assigned and/or hired to work in states where it is required by law to include a reasonable estimate of the compensation for any given position, compensation ranges are specific to those states and takes into account various factors that are considered in making compensation decisions, including but not limited to a candidate’s relevant experience, qualifications, skills, competencies, and proficiencies for the role.

Director of Risk Management and Quality Assurance

Advantage Care Health Centers

Brookville, New York

Overview: The Director of Risk Management & Quality Assurance oversees the daily clinical operations and coordinates all services at the federally qualified health center to ensure continuous quality improvement while remaining compliant with all state and federal regulations. • A minimum of five years of progressive leadership experience in healthcare operations, risk management, or quality assurance, within a Federally Qualified Health Center (FQHC) or comparable community‑based healthcare organization.

Director of Clinical Education and Quality Assurance 4015

Hatch Global Search

$90000 - $95000

Ocala, Florida

The Director of Clinical Training and Quality Assurance is available during normal operating hours and works closely with the Director of Clinical Services, the compliance team, and other regional staff to facilitate the ongoing needs of the staff and patients. The Director of QA and Clinical Training is responsible for the training and professional development of the clinical staff and ongoing administration of the performance improvement (PI)/quality assurance (QA) program in the home health agency.

Senior Director of QA Operations DSM (Drug Substance Manufacturing)

Fujifilm

Holly Springs, NC

Ensures the quality assurance (QA) review and approval of exceptions and CAPAs, while also facilitating the timely review and approval of process performance qualification (PPQ) protocols and reports, continuous process monitoring protocols and reports, risk assessments, changeover processes, equipment release, and sample plans. As part of the site Quality leadership team, the Sr Director, QA Ops DSM contributes to the cohesive implementation of quality systems across the Holly Springs, NC site, and ensures alignment with organizational goals and regulatory requirements.

Director of Food Safety & Quality Assurance - Operations

Grimmway Enterprises

$135000 - $170000

Arvin, California

Director of Quality & Risk Management Assurance

Sherman Oaks Hospital

$87048 - $115273.6

Sherman Oaks, California

Staffed with over 500 employees and an extraordinary team of physicians, the hospital is recognized for advanced technology and compassionate care and provides 24/7 emergency care in addition to a full range of specialized medical, surgical, and diagnostic services to improve and save lives. The exact starting compensation to be offered will be determined at the time of selecting an applicant for hire, in which a wide range of factors will be considered, including but not limited to, skillset, years of applicable experience, education, credentials and licensure.

Director Quality (Quality Assurance/Quality Control) - CIS

M.C. Dean, Inc

Tysons , Virginia

M.C. Dean is headquartered in Tysons, Virginia, and employs more than 5,800 professionals who engineer and deploy automated, secure, and resilient power and technology systems; and deliver the management platforms essential for long-term system sustainability. Lead the development, deployment, and governance of the SBU Quality Management Framework, institutionalizing the end-to-end quality lifecycle—from project selection through control execution, auditing, reporting, and continuous improvement.

Senior Director, QA Design Quality & Risk Management

West Pharmaceutical Services

Exton, PA

They will lead a team who provide quality compliance oversight to the network of Design Centers at the corporate level and support for the Operational Units’ level Design Center QMS which supports multiple concurrent development programs including medical devices, pharmaceutical combination products, and Containment. Oversee and provide direction to cross-functional teams on design control and QMS elements including but not limited to change control, training, CAPAs, issue reviews, audit findings, investigations, risk management activities, document control, configuration control, and quality agreements.

Director Quality Assurance

Imperative Care

Campbell, CA

What You’ll Bring: Bachelor’s degree in engineering or related discipline and a minimum of 10 years of progressive responsibility in quality assurance in a medical device, regulated or robotics setting, plus a minimum of 3 years of prior people management experience; or equivalent combination of education and work experience. As a key leader, this role takes part of strategic conversations and activities that include building a quality infrastructure aimed at transferring operations from concept to manufacturing in collaboration with robotics upper management and consultants.

Director, Clinical Quality Assurance

Cellectis

Raleigh, NC

The Director, Clinical Quality Assurance is primarily responsible for establishing and leading the Clinical QA function and providing independent oversight of Good Clinical Practices (GCP) activities to ensure compliance with FDA, EMA, ICH, and other applicable global and national regulatory requirements across Cellectis’ clinical programs. Knowledge and understanding of regulations regarding cell/gene therapies including but not limited to ICH guideline, GCP, and GMP as defined by the US Food and Drug Administration and European Medicines Agency.

Director Quality Assurance and Project Management Office

Express

Columbus, OH

Strong software development skillset, project management skills and have proven success in driving multiple large enterprise initiatives throughout the full lifecycle within an Agile product development environment; building and managing a team of employees and consultants; managing budgets and internal and external resources; managing, escalating and resolving risks/issues, and status reporting to senior management; and implementing, upgrading and maintaining eCommerce platform and systems . This position will also be responsible for developing PMO processes and policies, collaborating with technology and business leaders to create and manage the project portfolio, and applying project delivery framework to provide consistent structure while enabling agility within project teams.

Senior Director, GMP Quality Assurance

Umoja Biopharma

$234260 - $289380

Louisville, CO

As a senior leader within the company and Quality organization, this role will provide strategic leadership and direction, collaborating across all relevant internal and external stakeholders (e.g., Manufacturing, Supply Chain, Facilities & Engineering, CMC, Regulatory, etc.) to develop high performing & collaborative teams and mature and execute a comprehensive functional vision in alignment with company and organizational goals. This role shall also serve as a member of the senior Quality Leadership Team to set and execute strategic initiatives, maintain and encourage a strong continual improvement mindset, and serve as a critical leader in establishing, maturing, and championing Umoja's quality culture.

Sr. Director, Clinical Quality Assurance

Beam Therapeutics

$250000 - $310000

Cambridge, MA

Responsibilities include supporting and enabling appropriate Quality review of regulatory submissions, health authorities' (i.e. pre-filing meeting, filings, approval negotiations, post marketing commitments, annual reports, responses to questions, responses, and progress reports for regulatory commitments), and ensuring submissions are in line with the overall product strategy. Beam's suite of gene editing technologies is anchored by base editing, a proprietary technology that is designed to enable precise, predictable and efficient single base changes, at targeted genomic sequences, without making double-stranded breaks in the DNA.

Sr. Director, Food Safety & Quality Assurance

Kinder's

$200000 - $250000

Walnut Creek, CA

This role plays a critical leadership position in defining and scaling Kinder's quality systems, ensuring that every product delivered to market is safe, compliant, and consistently exceptional in taste and performance. Most of our work happens in the office to spark creativity and community, but we also offer flexibility so team members have the autonomy to work outside the office when needed to support their work-life balance and personal commitments.

Assistant Director, Quality Assurance & Control- Winship Cancer Institute

Emory University

Atlanta, Georgia

Cancer care at Winship includes leading cancer specialists collaborating across disciplines to tailor treatment plans to each patient’s needs and type of cancer; innovative therapies and clinical trials; comprehensive patient and family support services; and a personalized care experience aimed at easing the burden of cancer. Dedicated to discovering cures for cancer and inspiring hope, Winship Cancer Institute of Emory University is Georgia’s only National Cancer Institute-designated Comprehensive Cancer Center, a prestigious distinction given to the top tier of cancer centers nationwide for making breakthroughs against cancer.

Director Quality Assurance & Regulatory Affairs

OneBlood

Orlando, Florida

Ten (10) or more years of progressively responsible management experience in quality & regulatory affairs, preferably in a blood bank environment; or an equivalent combination of education, certification, training, and/or experience. Bachelor’s degree in medical technology, healthcare, chemistry, biology, biotechnology or related field from an accredited college or university; Master’s degree preferred.

Director, GCP Quality Assurance

Septerna

$220000 - $240000

South San Francisco, CA

The ideal candidate will collaborate closely with clinical study teams and cross-functional partners, fostering a culture of quality and maintaining a state of continual GCP compliance across all programs. To join our ambitious team, be prepared to bring your real self to work every day; grow and learn from a talented team of drug hunters, scientists, and business professionals; and contribute your passion, creativity, and energy to accomplish our mission.

Director, Quality Assurance

Wipfli Advisory LLC

$156000 - $210000

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Director Quality Assurance and Project Management Office

Express & Bonobos

Columbus, OH

Director - Quality Assurance

JBS USA

Ellijay, GA

EDUCATIONAL REQUIREMENTS: Bachelor of Science Degree in Food Science, or similar field; or five (5) years related experience and/or training, or equivalent combination of education and training. Ability to collect and analyze data using basic statistics, draw conclusions based on facts, and write succinct reports.

Assistant Director, Quality Assurance & Control- Winship Cancer Institute

Emory Healthcare/Emory University

Atlanta, GA

Director / Head Quality Assurance

OQSIE

Ocean City, MD

Quality Head/ Interiem Director provides strategic leadership and direction to the Quality Unit (e.g., GMP, GLP) comprising of the Quality Control and Quality Assurance departments. Past Quality / Compliance Director preferred, past Senior Manager with appropriate experience and ready for Director level could work.

Sr. Director, Quality Assurance

Presidio Medical, Inc.

$240000 - $275000

San Mateo, CA

Direct all administrative activities associated with the department, including establishing departmental goals and objectives; prepare and maintain operating, expense and capital budgets; issue relevant operating procedures; and recruit, train and assess key department personnel. Possess management leadership experience as a Senior Director of Quality and Compliance, with a strong cross-disciplinary understanding of an entire business entity, including Research & Development, Clinical, Marketing, Operations, Manufacturing, and Regulatory.

Director, Clinical Quality Assurance

Eisai

Nutley, NJ

The Director, Clinical Quality Assurance position is responsible for design, delivery and execution of the North America (NA) Clinical Quality Assurance (CQA) strategy including audit and inspection management and oversight of the Quality management system. E-Verify is an Internet based system operated by the Department of Homeland Security in partnership with the Social Security Administration that allows participating employers to electronically verify the employment eligibility of all new hires in the United States.

Director Quality Assurance

Qpex Biopharma, Inc

$200000 - $240000

San Diego, California

Working closely with executive leadership, Regulatory Affairs, Shionogi Quality partners, CMOs, and external consultants, this role ensures quality oversight across development, manufacturing, testing, and product release activities. The position leads internal teams and external vendors, supports regulatory submissions and inspections, and drives continuous improvement of quality systems to enable successful regulatory approvals and commercialization.

Quality Assurance Director - Construction

F.A. Wilhelm Construction Co., Inc.

Lafayette, IN

As a Quality Assurance Director, your key responsibility will be to help create, plan, manage, and enforce Wilhelm's Quality Assurance Program for the assigned project(s) by preventing "Q" issues, making observations, identifying potential issues, then creating/implementing a specific plan in order to eliminate any errors that could result in a quality deficient product. Manage self-perform and subcontracted work through Project Specific Quality Plans including Inspection and Test Plans, Check lists, proper training, and mock-ups, etc.

Regional Quality Assurance Director

Community Options, Inc.

$78000 - $80000

Princeton, NJ

Develop, coordinate, and participate in educational and training programs that focus on elements of Medicaid compliance, and strive to ensure that all appropriate employees and management are knowledgeable of and comply with pertinent federal and state health care program requirements. Ability to present information, communicate effectively, and respond with questions from groups of managers, people supported, general public, families, advocates and other stakeholders.

Director - Design Quality Assurance - Tissue Technologies

Integra LifeSciences

$166750 - $228850

Princeton, NJ

These activities include the development, implementation, and monitoring of quality programs and policies that ensure the development, manufacture, and distribution of medical devices in compliance with corporate policies, U.S. Food and Drug Administration regulations, ISO 13485, the Canadian Medical Device Regulations (CMDR), the EU Medical Device Regulation, Japanese Pharmaceutical Affairs Law, and other applicable global regulatory agencies. The Director, Design Quality Assurance (DQA) - Tissue Technologies division has the primary responsibility to ensure the delivery of high-quality design history files (DHF) and Risk management files (RMF) that are compliant with applicable global regulations.

Quality Assurance and Compliance Director

CBEM LLC

Lafayette, CA

Audit & Data Integrity: Oversee company-wide audit systems and EHR management, ensuring complete data integrity, regulatory compliance, and audit readiness. We are seeking a Strategic Quality Assurance & Compliance Director to lead our Quality Assurance team and serve as a vital member of our Senior Management Team (SMT).

Director, Quality Assurance

Cook Group

Bloomington, IN

Oversee the adequacy and maintenance of the QMS in meeting the requirements of the Cook entities and liaise with external accredited agencies • Ensure that reports are made to Management with Executive Responsibility (MER) on its performance, status and areas that require improvement • Ensure that awareness of regulatory and customer requirements is communicated with both staff and Management • Assist in establishment, maintenance and adequacy of the QMS• Foster and maintain a workplace culture respectful and supportive of individual differences• Must work and interact effectively and professionally with and for others throughout various levels of the global organization• Must maintain all training requirements for the position, while seeking out opportunities for continuous development and growth• Adhere to the Quality Management System to ensure meeting FDA 21 CFR 820, ISO 13485, and other applicable regulatory requirements, driving quality throughout the organization. • Bachelor's degree in related field or experience of such kind and amount as to provide a comparable background• Master's degree preferred• 10+ years of related industry experience• 5+ years in a leadership role.

Quality Assurance Director

AECOM

Washington, DC

We invite you to bring your bold ideas and big dreams and become part of a global team of over 50,000 planners, designers, engineers, scientists, digital innovators, program and construction managers and other professionals delivering projects that create a positive and tangible impact around the world. + Conduct inspection and investigations and tests that are of considerable complexity, such as of the contractor’s on-site plant (storage yards and temporary facilities), materials and equipment + Serve in oversight of final inspections, preparation of final punchlist and determination as to the completeness and acceptability of the Work.

QA Director/Capital Markets

Syntricate Technologies Inc

$210000 - $230000

Jersey City, NJ

Candidates must Build out a QA team to support the front, middle and back office systems as well as Identify and build a strategy for testing, test automation, defect tracking and integrated testing. Candidates must have director level or higher experience and recent experience working on trading platforms in capital markets or investment banking enterprises.

Director Division Quality Assurance - Rehab Services

State of Maine

$68993.59 - $97635.2

Augusta, Maine

A Bachelor's Degree in Business Administration, Social Work and/or Rehabilitation Services and (6) years of progressively responsible experience in business/program management that demonstrates a thorough knowledge of current systems improvement and project management concepts and the ability to develop and implement strategic plans for a major public service delivery system, which includes a minimum of two (2) years experience in an administrative, supervisory, or consultative capacity and two (2) years of experience in supervising professional staff providing social services and/or rehabilitation services programs is required. The successful candidate will have a proven track record of directing quality assurance and service improvement activities and will be able to demonstrate understanding and experience integrating technologies and processes that reflect current best practice.

Director, Quality Assurance – Clinical and Nonclinical Development

Prime Medicine

$207000 - $253000

Watertown, MA

Establish and maintain systems and processes (including SOP development) to improve the quality and compliance of both clinical and nonclinical studies, providing oversight and support to CRO GLP studies and internal non-GLP study activities in both the United States and Rest of World (ROW). This role will partner strategically with Clinical Development and Nonclinical functions to establish and maintain pragmatic, risk-based quality frameworks that ensure regulatory compliance and data integrity from early development through clinical execution.

Associate Director - QA IAPI

Lilly

$118500 - $173800

Indianapolis, IN

Our current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women’s Initiative for Leading at Lilly (WILL), enAble (for people with disabilities). The Associate Director – Quality Assurance (QA) is responsible for managing the activities of QA personnel supporting the oversight of Insulin Active Pharmaceutical Ingredient (API) manufactured within Indianapolis Active Pharmaceutical Ingredient (IAPI) manufacturing site.

Senior Director, Clinical Quality Assurance - Remote-Based

Eisai

Nutley, NJ

The Clinical Quality Assurance Professional (QAP) position is responsible for design, delivery and execution of the global Clinical Quality Assurance (CQA) strategy including audit and inspection management, issue management and oversight of the Quality management system. Direct and drive design, delivery, and execution of the global Clinical Quality Assurance (CQA) strategy for the country/region in scope (including audit and inspection management, issue management, and oversight of the quality management system).

Director, Post Market Quality Assurance

Cook Group

Bloomington, IN

Oversee and ensure that all post market quality activities comply with applicable regulations, including but not limited to: ISO13485, US FDA CFR Part 820, State Council Order No. 739- China, PMD Act, Law Act 145- Japan, Medical Device Management Act- Taiwan, Medical Devices Act- Korea, Good Distribution Practices-Thailand, etc. This role provides leadership and direction to global Quality Assurance teams by inspiring international teams, fostering a culture of collaboration, accountability, and high performance to ensure consistent delivery of centralized capabilities across all markets, leading to positive customer experiences.

Director, Quality Assurance

Brivo

Austin, Texas

To keep our global teams connected and inspired, we provide a premium onsite experience featuring communal meals, recurring social events, and fully stocked workspaces—ensuring you have everything you need to stay focused while building the future of security. Brivo is seeking a visionary Director of Software Quality Assurance to lead and scale our global QA strategy across a diverse and cutting-edge portfolio of cloud software, mobile/web client applications, and integrated hardware.

Director, Regulatory Affairs & Quality Assurance

Kemin

Off-site, undefined

Overview: The Regulatory & Scientific Affairs Director is responsible for leading the business units’ regulatory affairs (RA) and quality assurance (QA) teams by proactively ensuring regulatory and quality compliance, scientific integrity, and managing regulatory/quality risks and opportunities aligned with strategic direction and priorities of the business. Qualifications: Education and Experience:Advanced degree (MS, PhD, DVM, or JD) in a scientific, technical, or regulatory field strongly preferred, with 10+ years of progressive leadership experience in regulatory affairs, quality assurance, or compliance within pharmaceuticals, nutraceuticals, biotechnology, or food ingredient industries.

Associate Director, Clinical Quality Assurance

Kura Oncology

$170000 - $190000

Boston, MA

Enrollment in a Phase 2 registration-directed trial of ziftomenib in R/R NPM1-mutant AML has been completed, and in the second quarter of 2025, the companies announced the FDA's acceptance of a New Drug Application for ziftomenib for the treatment of adult patients with R/R NPM1-mutant AML and assignment of a Prescription Drug User Fee Act target action date of November 30, 2025. Reporting to the Executive Director of R&D Quality Assurance, the Associate Director, Clinical Quality Assurance (CQA) is responsible for supporting the development and implementation of processes and programs that provide quality and compliance oversight utilizing proactive end to end strategies for all clinical development programs, and pharmacovigilance activities.