Eli Lilly and Company · 3 hours ago
Associate Director - Quality Control Laboratories
Indianapolis, IN
Full-time
Onsite
Lead/Staff, Director/Executive
$123K/yr - $180K/yr
5+ years expEli Lilly and Company is a global healthcare leader headquartered in Indianapolis, Indiana. The Associate Director - Quality Control leads all aspects of laboratory testing in support of manufacturing operations, ensuring compliance with quality principles and GMPs while managing staff and resources effectively.
BiotechnologyHealth CareMedicalPharmaceutical
Responsibilities
Responsible for maintaining a safe work environment, leading safety initiatives, and working safely and accountable for supporting all HSE Corporate and Site Goals
Recruit / retain effective diverse staff; supervise, coach, and aid in development, performance management, ensure a fair and equitable work environment
Assist in the setting of human resource and business plan goals
Ability to lead and manage complex change agendas in a fast-paced environment, while delivering on multiple priorities
Apply knowledge of quality principles and GMPs toward the development of local procedures
Define and supervise quality plans for analytical projects to ensure accurate priority, resources, and direction have been provided
Interact effectively with customer and support groups
Define and maintain inspection readiness activities
Network with other areas to understand best practices, share knowledge, assist in tactical and strategic business planning, and to ensure customer needs are met
Influence development of improved and streamlined quality systems
Serve as conduit for corporate communications / initiatives
Serve as technical resource and review and approve technical documents
Facilitate assessment of assay variability contribution to total process variability and ensure lab initiatives are aimed at reducing measurement variability
Define, lead and/or support inspection readiness activities for lab operations and interact with Regulatory agencies during inspections
Network with other sites regarding new systems development
Work cross functionally at the site and global level to ensure recapitalization of equipment
Review and approve technical and GMP documents such as protocols, deviations, changes, summary reports, etc
Maintain open communications and promote teamwork and employee collaboration in the work group
Qualification
Required
Bachelor of Science in Chemistry / Biology / Microbiology or related science
5+ years GMP laboratory experience
Preferred
Effective time management
Deep understanding of compliance requirements and regulatory expectations
Effective problem-solving and teamwork skills
Strong self-management and organizational skills
Benefits
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
Well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities)
Company
Eli Lilly and Company
We're a medicine company turning science into healing to make life better for people around the world.
10001+ employees
H1B Sponsorship
Eli Lilly and Company has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (514)
2024 (236)
2023 (167)
2022 (133)
2021 (57)
2020 (52)
Funding
Current Stage
Public CompanyTotal Funding
$6.5M2024-02-12Post Ipo Debt· $6.5M
1978-01-13IPO
Leadership Team
David Ricks
Chair, CEO
Lucas Montarce
Executive Vice President and Chief Financial Officer
Recent News
2025-12-30
2025-12-30
Company data provided by crunchbase