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Associate Director, Quality Assurance (QA) – Change and Deviation Program Owner, Global API Network Expansion

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.

Associate Director, Quality Assurance (QA) – Change and Deviation Program Owner, Global API Network Expansion

Responsibilities:

The Deviation Management Program Owner is a key member of the QA & Compliance team, responsible for overseeing the site deviation management program to ensure product quality and safety. This role involves developing procedures, training materials, qualifying lead investigators, facilitating deviation review meetings, monitoring program performance, and representing the site program during regulatory inspections. Additionally, the Program Owner will collaborate with site inspection readiness teams and provide guidance to lead investigators, functional leaders, and senior quality leadership.

Key Objectives/Deliverables:

Program Development & Strategy

  • Work with Network Leadership and Site Quality Leaders to shape the vision, strategy, and quality culture for deviation and change management programs.
  • Serve as a technical resource for reviewing and approving program documentation (e.g., strategies, procedures, and policies).
  • Collaborate with cross-functional teams to establish and continuously improve deviation and change control quality systems.
  • Support recruiting efforts and build capability for a diverse leadership and quality assurance team.

Operational Readiness & Compliance

  • Establish site programs by partnering with other Lilly manufacturing sites and global materials management teams.
  • Develop and implement operational readiness plans for deviation and change control programs.
  • Foster a strong quality culture by promoting open communication, teamwork, and employee engagement in site workflows.
  • Participate in tactical and strategic business planning related to deviation and change control.

Deviation & Change Control Management

  • Prepare and author deviation management and change control procedures and training materials in compliance with Lilly’s Global Quality Standards and cGMP requirements.
  • Develop a qualification program for deviation lead investigators and change owners.
  • Establish standard processes for investigation forums, including triage meetings, impact assessments, investigation strategy sessions, root cause analysis, and CAPA alignment meetings.
  • Provide technical guidance to lead investigators in deviation investigations, quality impact evaluations, root cause analysis, and technical writing.

Performance Monitoring & Approval Responsibilities

  • Measure, monitor, and report Key Performance Indicators (KPIs) to Site Management.
  • Review and approve deviation investigations as a technical or quality approver, including observation deviations and moderate deviations.

Basic Requirements:

  • Bachelor's degree in science, engineering, or a pharmaceutical-related field or equivalent experience.
  • 5+ years of pharmaceutical leadership experience in deviation and change control QA, including working with cross-functional teams.

Additional Skills/Preferences:

  • Commitment to maintaining Lilly’s training requirements.
  • Strong knowledge of Quality Management Systems and regulatory requirements.
  • Experience in deviation and change control management.
  • Familiarity with Veeva QDocs, TrackWise, or similar systems.
  • Excellent interpersonal, written, and verbal communication skills.
  • Strong technical aptitude with the ability to train and mentor others.
  • Demonstrated technical writing, problem-solving, and decision-making skills.
  • Experience with facility or area start-up activities.
  • Previous experience in regulatory inspection readiness and execution.

This role is located in Indianapolis, IN and is not eligible for remote work.

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

$151,500 - $222,200

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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Average salary estimate

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$151500K
$222200K

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What You Should Know About Associate Director, Quality Assurance (QA) – Change and Deviation Program Owner, Global API Network Expansion, Eli Lilly and Company

At Lilly, an esteemed global healthcare leader based in Indianapolis, Indiana, we are on a mission to unite caring with discovery, striving every day to enhance lives. We're seeking an Associate Director, Quality Assurance (QA) – Change and Deviation Program Owner, Global API Network Expansion to join our team. In this pivotal role, you'll serve as a crucial member of our QA & Compliance team, overseeing the site deviation management program to ensure the highest standards of product quality and safety. Your day-to-day responsibilities will include developing procedures and training materials, qualifying lead investigators, and leading deviation review meetings. You'll collaborate with cross-functional teams to forge a culture of quality and engagement, aiding in the development of operational readiness plans and helping recruit diverse leadership talent. With responsibilities encompassing technical resource support, KPI monitoring, and regulatory inspections, you’ll have the opportunity to make a significant impact on our company's operations. Your expertise will guide the site in maintaining compliance with global quality standards, while fostering a robust quality culture through open communication and teamwork. If you're someone who's passionate about leading quality assurance efforts and committed to excellence in the pharmaceutical industry, consider bringing your talents to Lilly - where every day, we work together to make life better for people around the world. Join us in creating solutions that will change lives for the better!

Frequently Asked Questions (FAQs) for Associate Director, Quality Assurance (QA) – Change and Deviation Program Owner, Global API Network Expansion Role at Eli Lilly and Company
What are the key responsibilities of the Associate Director, Quality Assurance (QA) at Lilly?

The Associate Director, Quality Assurance (QA) at Lilly is responsible for overseeing the site deviation management program to ensure product quality and safety. This includes developing procedures and training materials, qualifying lead investigators, facilitating deviation review meetings, and monitoring program performance. The role also involves collaboration with cross-functional teams and representation during regulatory inspections, all aimed at fostering a strong quality culture.

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What qualifications are required for the Associate Director, Quality Assurance (QA) role at Lilly?

Candidates for the Associate Director, Quality Assurance (QA) position at Lilly must possess a Bachelor's degree in science, engineering, or a pharmaceutical-related field, complemented by at least 5 years of leadership experience in deviation and change control QA. Strong knowledge of Quality Management Systems, regulatory requirements, and experience in deviation and change control management are also essential for this role.

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How does the Associate Director of Quality Assurance contribute to compliance at Lilly?

The Associate Director, Quality Assurance at Lilly plays a vital role in ensuring compliance by establishing site programs and developing operational readiness plans that align with Lilly’s Global Quality Standards and cGMP requirements. They prepare and approve deviation management procedures, advise on investigations, and monitor performance indicators to uphold compliance and safety.

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What skills are preferred for the Associate Director, Quality Assurance (QA) at Lilly?

Preferred skills for the Associate Director, Quality Assurance (QA) position at Lilly include strong interpersonal and communication abilities, technical writing proficiency, problem-solving skills, and experience in regulatory inspections. Familiarity with industry systems like Veeva QDocs and TrackWise is advantageous, along with the capability to train and mentor team members and maintain objectives for recruiting diverse talent.

Join Rise to see the full answer
What is the expected salary for the Associate Director, Quality Assurance (QA) position at Lilly?

The anticipated salary for the Associate Director, Quality Assurance (QA) role at Lilly ranges from $151,500 to $222,200, depending on a candidate's education, experience, skills, and geographic location. Additionally, full-time employees may be eligible for a company bonus and a comprehensive benefits program that supports their well-being and financial security.

Join Rise to see the full answer
Common Interview Questions for Associate Director, Quality Assurance (QA) – Change and Deviation Program Owner, Global API Network Expansion
Can you describe your experience with deviation management and how it relates to the Associate Director, Quality Assurance role?

In answering this question, highlight specific instances where you've successfully managed deviations, emphasizing your understanding of the processes and impact on product quality. Discuss your approach to creating procedures and fostering a quality culture, which is critical for the Associate Director position.

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How do you ensure compliance with regulatory standards in quality assurance?

Detail your strategies for staying updated on regulatory requirements, and mention any systems or processes you've implemented in past roles. Discuss your experience in audit preparation and how you have fostered a culture of compliance among team members.

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What techniques do you use to foster teamwork and communication in your quality assurance team?

Provide examples of how you have created open lines of communication within your team, such as regular check-ins or collaborative training sessions. Highlight the value of teamwork in achieving quality objectives, which is vital for the Associate Director role.

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Can you discuss a situation where you led a successful quality improvement initiative?

Use this opportunity to describe a specific project where you took the lead on quality improvement. Explain the steps you took, the challenges faced, and the measurable outcomes that were achieved, demonstrating your leadership capabilities relevant to the Associate Director position.

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What do you believe is the most important aspect of quality culture in a pharmaceutical setting?

Emphasize the significance of open communication and shared accountability as foundational to a strong quality culture. Discuss specific actions you would take as Associate Director to promote this culture at Lilly, aligning your answer with the company’s values.

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How do you prioritize tasks within a busy quality assurance environment?

Explain your methods for task prioritization, such as assessing the urgency and impact of each task. Share any tools you use for time management and highlight the importance of aligning priorities with the company’s quality objectives.

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Describe your experience with technical writing in quality procedures.

Focus on your ability to create clear and effective operational documents. Mention specific examples of procedures you've authored and how the technical writing contributed to achieving compliance and enhancing team performance.

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What role does data analysis play in your decision-making process regarding quality initiatives?

Discuss how you leverage data analysis to inform your quality assurance decisions. Provide an example of a data-driven initiative you've implemented, showcasing your analytical skills necessary for the Associate Director role.

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How do you mentor others in your team to improve their quality assurance skills?

Talk about your mentoring approach, including providing constructive feedback, setting learning objectives, and creating development plans. Highlight the importance of nurturing talent in building a competent quality assurance team.

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What strategies do you employ to keep abreast of industry best practices in quality assurance?

Mention any professional organizations you belong to, conferences you attend, or literature you read. Describe your commitment to continuous learning, which is crucial in the evolving pharmaceutical quality landscape.

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We make medicines that help people live longer, healthier, more active lives.

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March 31, 2025

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