Senior Director, Manufacturing & Quality Learning Standardization Lead

Lilly • Indiana, Indiana • 1w ago

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.

About the Role:

The Director - Manufacturing & Quality, Training Globalization and Standardization will play a critical role in leading the implementation of One QMS and QMS I3 across 23 global manufacturing sites, as well as central functions. This individual will serve as the primary driver for standardizing and globalizing quality-related training processes, ensuring consistent execution, adoption, and sustainment across the network. Additionally, this role will ensure site alignment, readiness and scalability.

Key Responsibilities

Oversee the training related to the global implementation of standardized processes and coordinating deployment efforts across 23 manufacturing and quality sites.

Lead the harmonization and standardization of manufacturing-related quality training processes to drive consistency, compliance, and operational excellence.

Serve as the key liaison between global central functions and site training quality leads to ensure training alignment, execution, and best practices.

Own and maintain the integrated training roadmap, timelines, milestones, risk mitigation, and issue resolution across all participating sites.

Monitor implementation progress, adoption metrics, and readiness indicators to ensure sustainable execution.

Provide direction and support for local site readiness, including change management, communication, and capability-building.

Lead the expansion and standardization of training related to additional quality processes under the QMS I3 framework.

Collaborate cross-functionally with MQ L&D Network Leaders, Tech@Lilly, Quality Systems, Site Quality Leaders, and Global Process Owners to ensure seamless execution.

Develop dashboards and reporting tools to track implementation health and escalate risks/barriers to leadership.

Basic Qualifications :

Bachelor's degree in Life Sciences, Engineering, Quality, or related field

8+ years of experience in pharmaceutical manufacturing, manufacturing or quality roles

Qualified applicants must be authorized to work in the United States on a full-time basis. Lilly will not provide support for or sponsor work authorization and/or visas for this role.

Preferred Qualifications

Demonstrated experience with large-scale systems implementation (preferably QMS or LMS)

Strong background in GxP, L&D, quality systems, and regulatory compliance

Advanced degree or certifications in Quality Management, Regulatory Affairs, or related discipline

Proven track record of deploying quality systems globally across multiple sites

Strong project management and change leadership skills

Effective communicator with the ability to engage and influence senior stakeholders across a global network

Experience working in a matrixed organization and leading cross-functional teams

Working knowledge of systems like Veeva, TrackWise, SuccessFactors LMS, or equivalent

Additional Information:

Travel required (domestic and international), may be up to 40%

Role may be based in a major hub site or remotely with global coordination responsibilities

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

$150,000 - $220,000

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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