1

Associate Director Quality Assurance Jobs in Indiana

As our Director of Quality Assurance you will report directly to the site General Manager, as a senior staff member. You'll be responsible to lead a team of managers that direct quality control ...

As our Director of Quality Assurance you will report directly to the site General Manager, as a senior staff member. You'll be responsible to lead a team of managers that direct quality control ...

As Senior Director, Quality for our Mount Vernon site, you will lead the end-to-end Quality ... Multiple experiences within pharmaceutical QA and/or operations. * Experience in dealing with ...

As Senior Director, Quality for our Mount Vernon site, you will lead the end-to-end Quality ... Multiple experiences within pharmaceutical QA and/or operations. * Experience in dealing with ...

As Senior Director, Quality for our Mount Vernon site, you will lead the end-to-end Quality ... Multiple experiences within pharmaceutical QA and/or operations. * Experience in dealing with ...

next page

Showing results 1-20

Associate Director Quality Assurance information

See Indiana salary details

$12

$27

$59

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

As of Aug 29, 2026, the average hourly pay for associate director quality assurance in Indiana is $27.87, according to ZipRecruiter salary data. Most workers in this role earn between $17.84 and $32.69 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 Indiana?

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

What job categories do people searching Associate Director Quality Assurance jobs in Indiana look for?

The top searched job categories for Associate Director Quality Assurance jobs in Indiana are:

What cities in Indiana are hiring for Associate Director Quality Assurance jobs?

Cities in Indiana with the most Associate Director Quality Assurance job openings:

Infographic showing various Associate Director Quality Assurance job openings in Indiana as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 13% Part Time, 3% Contract, and 1% Nights. Highlights an 82% Physical, 3% Hybrid, and 15% Remote job distribution, with an average salary of $57,974 per year, or $27.9 per hour.

Associate Director - QA - LAPI

Eli Lilly and Company

Lebanon, IN • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 17 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, the work is demanding because patients are waiting. We unite caring with discovery to help make life better for people around the world, knowing that every decision, every detail, and every day matters. Headquartered in Indianapolis, Indiana, our over 50,000 employees around the globe take on complex challenges to discover and deliver life-changing medicines, strengthen how health is understood and managed, and support the communities we serve. This is hard, urgent, selfless work-but it's work worth doing. If you're driven by purpose and ready to bring your best to work that truly matters for patients, we invite you to join us.
Lilly is currently constructing an advanced manufacturing facility for production of API molecules located in Lebanon, IN. This facility is Lilly's largest investment in manufacturing capacity and is intended to provide APIs for current and future products, including new modalities. This is a unique opportunity to be a part of the site team for the startup of a greenfield manufacturing site, and the successful candidate will help to build the organization, the facility, and the culture to enable a successful startup into GMP manufacturing operations.
Position Brand Description:
The Associate Director - QA is a partner with the Sr. Director - QA in ensuring that operations have robust quality oversight. The Associate Director - QA is primarily responsible for the productivity and development of the QA employees, the quality of the product/results, oversight of manufacturing and support operations and overall customer service. It is expected that the Associate Director will oversee the department's performance, resolution of quality issues, and regulatory compliance.
Key Objectives/Deliverables:
  • Provide coaching/feedback to and develop QA employees.
  • Utilize Human Resources tools to ensure that the right individuals are in the right job (e.g., Performance Management, Merit Delivery, Talent Assessment, Succession Planning and Staffing).
  • Participate in organizational planning.
  • Provide input into the business plan and ensure conformance to department budget for area of responsibility.
  • Exhibit cross-functional influence.
  • Maintain and improve quality systems.
  • Approve deviations, procedures, protocols, and change controls.
  • Develop and maintain processes that support inspections and audits; prepare individuals to interact with auditors and inspectors.
  • Participate in self-assessments and regulatory agency inspections.
  • Ensure internal and external quality and supply commitments are met.
  • Provide quality management oversight for API manufacturing, laboratories, and warehouses.
  • Investigate complaints.
  • Manage the creation, revision, and maintenance of cGMP documents (e.g., job aids, procedures, forms, job descriptions).
  • Provide oversight and review of changes to the Global Quality Standards and ensure local implementation of changes.
  • Network with other sites regarding new or current quality systems.

Basic Requirements:
  • BS or equivalent in a scientific field or engineering.
  • 5+ years in CGMP Manufacturing.

Additional Preferences:
  • Knowledge of cGMPs.
  • Experience in Manufacturing, QC, QA, Technical Services, Engineering or Regulatory Affairs Leadership
  • Previous experience supervising/leading people.
  • Demonstrated strong written and verbal communications skills.
  • Strong attention to detail.
  • Understanding of statistical tools and analysis.
  • Excellent interpersonal skills and networking skills.
  • Ability to organize and prioritize multiple tasks.
  • Demonstrated strong problem solving and analytical thinking skills.
  • Ability to influence diverse groups.
  • Demonstrated understanding of computer applications.

Other Information:
  • Must complete Learning Plan for Associate Director - QA - LAPI.
  • No certifications required.
  • Tasks require entering manufacturing and laboratory areas which require wearing appropriate PPE.
  • Must support 24 hour/day operations.
  • Some travel may be required.

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 (AMECA), Black Employees at Lilly (BE@Lilly), Chinese Culture Network (CCN), EnAble, Evolve, Lilly Indian Network (LIN), Organization of Latinx at Lilly (OLA), Pride (LGBTQ+ Allies), Veterans Leadership Network (VLN) and Women's Initiative for Leading at Lilly (WILL).
Actual compensation will depend on a candidate's education, experience, skills, and geographic location. The anticipated wage for this position is
$123,000 - $180,400
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.
#WeAreLilly

What Eli Lilly and Company employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom


Eli Lilly logo

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