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Associate Director Quality Assurance Jobs (NOW HIRING)

Abbott

Director Quality Assurance

Casa Grande, AZ

Job Title Director Quality Assurance The Opportunity The Director Quality Assurance is responsible for managing the Quality Assurance Department and the Quality System to achieve compliance with ...

Abbott

Director Quality Assurance

Casa Grande, AZ · On-site

Job Title Director Quality Assurance The Opportunity The Director Quality Assurance is responsible for managing the Quality Assurance Department and the Quality System to achieve compliance with ...

Abbott

Director Quality Assurance

Casa Grande, AZ · On-site

Job Title Director Quality Assurance The Opportunity The Director Quality Assurance is responsible for managing the Quality Assurance Department and the Quality System to achieve compliance with ...

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

As of Aug 7, 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 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.

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:
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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 August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 14% Part Time, 4% Contract, and 1% Nights. Highlights an 90% Physical, 1% Hybrid, and 9% Remote job distribution, with an average salary of $60,925 per year, or $29.3 per hour.

Associate Director - Quality Assurance - Device Assembly

Eli Lilly and Company

Pleasant Prairie, WI • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 5 days ago

Eli Lilly and Company rating

8.8

Company rating: 8.8 out of 10

Based on 63 frontline employees who took The Breakroom Quiz

11th of 86 rated pharmaceutical

Job description

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We're looking for people who are determined to make life better for people around the world.

Organization Overview

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. .

Position Overview

Lilly is actively growing its manufacturing footprint globally to meet the needs of patients and deliver on our exciting future. As a result, Lilly is looking for experienced quality assurance leaders to support our growth in Kenosha County, Wisconsin. This is an outstanding opportunity to deliver on new manufacturing investments and new pioneering technologies.

The Associate Director, Quality Assurance (QA) - Device Assembly (DA), is responsible for staffing, training, and leadership of the quality assurance group supporting the start-up of combination product device assembly and operations at the Kenosha site. This individual is responsible for quality oversight of process development, operational readiness, qualification, and validation of the facility and its associated equipment. The Associate Director will help build a strong quality culture at the site and lead the QA team ensuring robust oversight and support of the ongoing operation as well as the site inspection readiness agenda.

Responsibilities

  • Support the Sr. Director, QA, in the development of the site organization, creation of the Quality Management System implementation plan, and execution of site quality operations in Device Assembly and Packaging (DAP).
  • Support the site to ensure a safe work environment including supporting and leading safety efforts for the quality team.
  • Support the development of the overall site operational readiness plan including development of quality processes and approval of operational procedures for DAP.
  • Build a diverse and capable site organization to provide quality oversight and ensure compliance with area procedures and controls for device assembly.
  • Foster a strong quality culture including maintaining open communications and promoting teamwork and employee participation in the work group.
  • Supervise, coach, and aid in development, performance management, ensure a fair and equitable work environment.
  • Engage team and delegate to achieve results through others to deliver according to plan.
  • Manage multiple priorities in a fast-paced environment and deliver in accordance with established due dates.
  • Demonstrate flexibility with quick response as priorities change or issues arise.
  • Partner with production and design organization to ensure 24/7 Quality oversight and support.
  • Engage and support Operational Excellence initiatives for monitoring performance and continuously improving the operation.
  • Review and approve GMP documentation including qualification/validation protocols and reports, procedures, deviations, technical reports, change controls, for DA operations.
  • Network with global and other DA sites to understand best practices, share knowledge.
  • Work cross-functionally with the area process teams/flow team for metrics reviews, operational support, and issue/deviation management.
  • Set area human resource and business plan goals.
  • Participate in tactical and strategic business planning.
  • Communicate on project and production status.
  • Define, lead and/or support inspection readiness activities for operations and interact with Regulatory agencies during inspections.


Basic Requirements

  • Bachelor's degree in a science, engineering, or pharmaceutical-related field of study or equivalent experience.
  • Minimum 5 years' experience in pharmaceutical leadership with QA experience, including leading or working effectively with a cross-functional group
  • Minimum 5 years' experience directly supporting a pharmaceutical manufacturing operation (preferably device assembly operations)
  • On-site presence required


Additional Skills/Preferences

  • Strong knowledge of Quality Management Systems and applicable regulatory requirements
  • Previous regulatory inspection readiness and inspection execution experience
  • Previous facility or area start up experience
  • Previous equipment qualification and process validation experience
  • Previous experience with SAP or other inventory management systems
  • Previous experience with highly automated combination products, packaging, and warehouse operations
  • Previous experience with Manufacturing Execution Systems and electronic batch release
  • Previous experience with automated material movement (central palletizing operation, automated warehousing)
  • Previous experience with deviation and change management systems such as Veeva
  • Excellent interpersonal, written and oral communication skills
  • Strong technical aptitude and ability to train and mentor others
  • Demonstrated technical writing skills
  • Demonstrated problem-solving and decision-making skills

Additional Information:

  • Flex hours possible
  • Primary location is Kenosha, Wisconsin
  • Ability to travel (approximately 10-20 %)
  • Ability for Short Term Assignment (6-9 Months) in a Device Assembly and Packaging site prior to starting the role

This job description is intended to provide a general overview of the job requirements at the time it was prepared. The job requirements of any position may change over time and may include additional responsibilities not specifically described in the job description. For GMP purposes, the job description should be updated for significant changes. As always, you should consult with your supervisor regarding your actual job responsibilities and any related duties that may be required for the position.

Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.

Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status.


Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. 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). Learn more about all of our groups.

Actual compensation will depend on a candidate's education, experience, skills, and geographic location. The anticipated wage for this position is

$123,000 - $198,000

Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly's compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees.

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About Eli Lilly

Sourced by ZipRecruiter

Eli Lilly, based in Indianapolis, IN, US, is one of the pioneers in the pharmaceutical industry with a rich history dating back to 1876. This global pharmaceutical company focuses on discovering, developing, manufacturing and selling pharmaceutical products in approximately 120 countries. The company's product categories include endocrinology, oncology, cardiovascular, neuroscience, and immunology. Having invested over $9 billion in research and development in the past decade, Eli Lilly is also committed to creating high-quality medicines that meet real needs. As a recipient of several awards and recognitions, Eli Lilly is known for its focus on life-saving research and drug development. Their mission is to make medicines that help people live longer, healthier, and more active lives.

Industry

Pharmaceutical product wholesalers

Company size

10,000+ Employees

Headquarters location

Indianapolis, IN, US

Year founded

1876

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