

New · posted Nov 11
Eli Lilly · Pharmaceuticals
Quality Assurance - NALO - Distribution
- Plainfield, IN
- On-site
- Full-time
- Associate & Specialist
The role
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.
Every dose that reaches a patient has to arrive with its quality intact. In this role, you'll be the quality voice for our commercial distribution network, making sure our North American Logistic Operation's warehouses, third-party logistics (3PL) partners, and distribution service providers meet GMP, GDP, and Lilly quality standards. You'll work hands-on with quality records, risk assessments, and metrics, and you'll build deep technical expertise in how a regulated distribution network runs.
Additional Preferences
- Prior Quality or Engineering experience working in Distribution, Medical Devices and providing oversight to 3PLs and Service Providers
- Prior FUME experience and understanding FUME requirements and regulations
- Knowledge and experience with CSQA and Data Integrity application
- Experience with ICH Q9 and/or Lilly's Quality Risk Management standards
- Clear understanding of all GMP/GDPs, policies, procedures, regulations and guidelines related to commercial distribution
- Knowledge and experience in quality records (Deviation, CC, PPE, SCN's, procedure, etc.)
- Effective communication, both written and oral
- Demonstrated ability to be self-driven, work independently, and apply time management and project management skills
- High-quality skills to include ability to prioritize, critical decision making, interpersonal/people, problem solving
- Strategic thinking and ability to influence diverse groups and communicate effectively to all levels of an organization internally and externally
- Strive to exceed individual and business goals and continuous improvement
What you need
Basic Requirements
- Bachelor's degree in pharmacy, Chemistry, Life Sciences, Engineering, or Supply Chain/Logistics
- One plus years of experience in quality assurance, distribution, or supply chain within the pharmaceutical or medical device industry.
- 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 or visas for this role, including but not limited to F-1 CPT, F-1 OPT, F-1 STEM OPT, J-1, H-1B, TN, O-1, E-3, H-1B1, or L-1.
What you'll do
- Make quality culture the foundation of your work, to ensure our products are delivered on time and in a safe and effective manner to improve patients' lives.
- Collaborate with site compliance leader and site data leader to ensure robust Quality System and Computer System Validation to ensure compliance and meet data integrity requirements.
- Understand NALO Operations to be able to provide quality oversight, identify and escalate potential Quality concerns, support meeting business goals and lead process improvement initiatives.
- Provide Quality oversight for NALO distribution operations network and maintain a state of inspection readiness for all distribution warehouses under NALO control. Support development of quality indicators/metrics to track Quality performance at all distribution locations.
- Collaborate both internally and externally to identify opportunities to standardize operations, increase global harmonization, and identify improvement opportunities.
- Apply Quality Risk Management principles to NALO operations, using Lilly quality standards. Author, review, and approve Risk Assessments to ensure adequate oversight including external monitoring of regulatory changes.
- Provide quality oversight and maintain the qualified status of distribution supplier and service provider per Supplier Quality Management System.
- Manage, investigate and document product and distribution complaint and monitor performance.
- Author, review and approve quality documents such as deviation investigations, change control activities, CARTS, PPE, SCN's, SOP, etc., with focus on issue resolution and continuous improvement.
- Develop and collect metrics related to the Quality performance within area of responsibilities. Provide updates to management and propose performance improvement.
- Support inspection readiness initiative and internal/external audits (site self-inspections; regulatory agencies and GQAAC).
- Support the Operations by:
- Timely and accurately completing all assigned tasks and responsibilities
- Collaborating with other functions, including hands-on work experience and shared learning
- Proposing solutions and benchmarking with other Lilly sites to gain support
- Other duties as assigned.
Pay and benefits
$66,000 – $171,600 a year
Employer providedAdditional Information
- This is an on-site, dayshift position, with occasional off-hours, weekend, and holiday support may be needed, including during Summer Shutdown, year-end, and the Christmas-New Year period.
- Position Location: Plainfield Distribution Center, Plainfield, Indiana
- Travel: 25-30% travel to regional distribution centers under NALO Quality oversight
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
$66,000 - $171,600
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.
Company bonus
401(k)
Pension
Vacation benefits
Medical, dental, vision and prescription drug benefits
Well-being benefits
Where you'll work
Plainfield, INOn-siteOpen in Maps (opens in a new tab)
More jobs in Plainfield, INJob intelligence
The context around this role
Live data · November 11, 2026
Salary intelligence
How the pay compares
This role's midpoint is 51% above the US median for Quality Assurance roles at this level.
This roleEmployer provided
Associate & Specialist roles in the US70 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| This role | $66,000 | — | $171,600 |
| All US (middle half) | $59,250 | $78,500 | $88,875 |
This role: Eli Lilly's own published range. Comparisons: the base pay employers published on open Quality Assurance roles at the same level on Regulatory Jobs, November 11, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Quality Assurance
The general path across 340 open Quality Assurance roles on Regulatory Jobs, with the titles they carry most. Not Lilly's own promotion track.
Skills DNA
What this role leans on
How many of the posting's 32 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- Quality systems and risk8
- GMP and compliance6
- Collaboration and leadership6
- Documentation and SOPs5
- Investigations and CAPA3
- Data and digital systems2
- Validation and qualification1
Regulatory intelligence
The rules, regulations and standards behind this role
The regulations, guidance and standards that govern Quality Assurance work in pharmaceuticals, led by the four this posting names, each linked to the agency or standards body that publishes it.
- FDA21 CFR Parts 210 and 211(official source, opens in a new tab)FDA current good manufacturing practice for finished pharmaceuticalsNamed in the posting
- ICHICH Q9(R1)(official source, opens in a new tab)Quality risk managementNamed in the posting
- FDAFDA data integrity guidance(official source, opens in a new tab)Data Integrity and Compliance With Drug CGMP: Questions and AnswersNamed in the posting
- EUEU Good Distribution Practice(official source, opens in a new tab)Guidelines on good distribution practice of medicinal products for human useNamed in the posting
- ICHICH Q10(official source, opens in a new tab)The pharmaceutical quality system across the product lifecycle
- FDA21 CFR Part 11(official source, opens in a new tab)FDA rules for electronic records and electronic signatures
- FDAFDA quality agreements guidance(official source, opens in a new tab)Contract Manufacturing Arrangements for Drugs: Quality Agreements
- FDAFDA Investigations Operations Manual(official source, opens in a new tab)How FDA investigators plan and conduct inspections
- FDA21 CFR 314.70(official source, opens in a new tab)Supplements and other changes to an approved application (post-approval CMC changes)
- ISOISO 19011(official source, opens in a new tab)Guidelines for auditing management systems
- ISPEISPE GAMP 5(official source, opens in a new tab)A risk-based approach to compliant GxP computerized systems
- EUEU GMP (EudraLex Volume 4)(official source, opens in a new tab)The EU's good manufacturing practice rules, including Annex 1 sterile and Annex 15 validation
- ICHICH Q7(official source, opens in a new tab)Good manufacturing practice for active pharmaceutical ingredients
- FDA21 CFR Part 7(official source, opens in a new tab)FDA enforcement policy, including product recalls
- PIC/SPIC/S(official source, opens in a new tab)The Pharmaceutical Inspection Co-operation Scheme and its GMP guide
- FDAFDA aseptic processing guidance(official source, opens in a new tab)Sterile Drug Products Produced by Aseptic Processing: Current Good Manufacturing Practice
Company hiring pulse
Lilly on Regulatory Jobs
- 53
- Open roles
- 53
- Distinct roles
- 10
- Locations
By discipline
- Quality29 55%
- Clinical17 32%
- Regulatory7 13%
By level
- Director24 45%
- Senior & Principal16 30%
- Associate & Specialist7 13%
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Quality Assurance - NALO - Distribution at Lilly
Open until filled. $66K–$172K a year, employer provided.


